5-Azidopyridin-1-Ium-5-I...
C6H6N4O2
5-Azidopyridin-1-Ium-5-I...
C6H6N4O2
Molecular Mass 166.137 g·mol−1 Heat of Formation 114.8 ± 16.7 kJ·mol−1 Dipole Moment 2.37 ± 1.08 D Volume 179.24 Å 3 1-(4-Azidophenyl)-2-Fluo...
C8H7FN3O
1-(4-Azidophenyl)-2-Fluo...
C8H7FN3O
Molecular Mass 180.159 g·mol−1 Heat of Formation 98.6 ± 16.7 kJ·mol−1 Dipole Moment 2.59 ± 1.08 D Volume 201.66 Å 3 (2s)-2-Azido-3-Phenylpro...
C9H10N3O2
(2s)-2-Azido-3-Phenylpro...
C9H10N3O2
Molecular Mass 192.195 g·mol−1 Heat of Formation 24.1 ± 16.7 kJ·mol−1 Dipole Moment 3.37 ± 1.08 D Volume 225.28 Å 3 3-(4-Azidophenyl)propano...
C9H10N3O2
3-(4-Azidophenyl)propano...
C9H10N3O2
Molecular Mass 192.195 g·mol−1 Heat of Formation -15.9 ± 16.7 kJ·mol−1 Dipole Moment 1.77 ± 1.08 D Volume 227.42 Å 3 (2s)-2-Amino-3-(3-Azido-...
C9H11N4O3
(2s)-2-Amino-3-(3-Azido-...
C9H11N4O3
Molecular Mass 223.209 g·mol−1 Heat of Formation -166.4 ± 16.7 kJ·mol−1 Dipole Moment 1.81 ± 1.08 D Volume 254.28 Å 3 (e)-(2-Methylphenyl)diaz...
C7H8N2
(e)-(2-Methylphenyl)diaz...
C7H8N2
Molecular Mass 120.152 g·mol−1 Heat of Formation 253.6 ± 16.7 kJ·mol−1 Dipole Moment 1.00 ± 1.08 D Volume 154.06 Å 3 (2s)-2-Amino-3-Azido-Pro...
C3H7N4O2
(2s)-2-Amino-3-Azido-Pro...
C3H7N4O2
Molecular Mass 131.113 g·mol−1 Heat of Formation -55.6 ± 16.7 kJ·mol−1 Dipole Moment 2.79 ± 1.08 D Volume 150.05 Å 3 4-Azido-N-[4-[(r)-[(1s,2...
C26H29IN6O3
4-Azido-N-[4-[(r)-[(1s,2...
C26H29IN6O3
Molecular Mass 600.451 g·mol−1 Heat of Formation 70.7 ± 16.7 kJ·mol−1 Dipole Moment 5.29 ± 1.08 D Volume 592.54 Å 3 N-[2-(4-Azidobenzyl)-3-S...
C12H15N4O3S
N-[2-(4-Azidobenzyl)-3-S...
C12H15N4O3S
Molecular Mass 295.338 g·mol−1 Heat of Formation -150.3 ± 16.7 kJ·mol−1 Dipole Moment 5.66 ± 1.08 D Volume 347.12 Å 3 4-Azido-2,3,5,6-Tetraflu...
C7H2F4N3O2
4-Azido-2,3,5,6-Tetraflu...
C7H2F4N3O2
Molecular Mass 236.103 g·mol−1 Heat of Formation -661.7 ± 16.7 kJ·mol−1 Dipole Moment 2.15 ± 1.08 D Volume 211.78 Å 3 4-Azidotetrafluorobenzoi...
C7H2F4N3O2
4-Azidotetrafluorobenzoi...
C7H2F4N3O2
Molecular Mass 236.103 g·mol−1 Heat of Formation -661.7 ± 16.7 kJ·mol−1 Dipole Moment 2.15 ± 1.08 D Volume 212.08 Å 3 (6r,7r)-3-[(2-{(e)-[4-(d...
C20H18N6O4S2
(6r,7r)-3-[(2-{(e)-[4-(d...
C20H18N6O4S2
Molecular Mass 470.525 g·mol−1 Heat of Formation 173.0 ± 16.7 kJ·mol−1 Dipole Moment 14.88 ± 1.08 D Volume 641.41 Å 3 (5-Azido-1h-Indol-3-Yl)a...
C10H9N4O2
(5-Azido-1h-Indol-3-Yl)a...
C10H9N4O2
Molecular Mass 217.204 g·mol−1 Heat of Formation 99.7 ± 16.7 kJ·mol−1 Dipole Moment 5.33 ± 1.08 D Volume 244.82 Å 3 (e)-Phenyldiazene
C6H6N2
(e)-Phenyldiazene
C6H6N2
Molecular Mass 106.125 g·mol−1 Heat of Formation 295.7 ± 16.7 kJ·mol−1 Dipole Moment 0.35 ± 1.08 D Volume 134.79 Å 3 4-Amino-1-[2-Azido-3-Hyd...
C10H7N6O3
4-Amino-1-[2-Azido-3-Hyd...
C10H7N6O3
Molecular Mass 259.201 g·mol−1 Heat of Formation 941.8 ± 16.7 kJ·mol−1 Dipole Moment 7.01 ± 1.08 D Volume 296.8 Å 3 3-(4-{(e)-[4-(dimethylam...
C17H17N5OS
3-(4-{(e)-[4-(dimethylam...
C17H17N5OS
Molecular Mass 339.415 g·mol−1 Heat of Formation 379.2 ± 16.7 kJ·mol−1 Dipole Moment 2.94 ± 1.08 D Volume 393.9 Å 3 1-{3-Azido-2,3-Dideoxy-5...
C16H10N6O5
1-{3-Azido-2,3-Dideoxy-5...
C16H10N6O5
Molecular Mass 366.288 g·mol−1 Heat of Formation 1575.9 ± 16.7 kJ·mol−1 Dipole Moment 10.62 ± 1.08 D Volume 365.56 Å 3 4-Azidobenzoyl Chloride
C7H5ClN3O
4-Azidobenzoyl Chloride
C7H5ClN3O
Molecular Mass 182.587 g·mol−1 Heat of Formation 223.1 ± 16.7 kJ·mol−1 Dipole Moment 2.84 ± 1.08 D Volume 194.61 Å 3 (z)-1-(4-Azidophenyl)-2-...
C8H10N5O
(z)-1-(4-Azidophenyl)-2-...
C8H10N5O
Molecular Mass 192.198 g·mol−1 Heat of Formation 512.3 ± 16.7 kJ·mol−1 Dipole Moment 3.32 ± 1.08 D Volume 212.24 Å 3 1-Azido-4-Isothiocyanato...
C7H5N4S
1-Azido-4-Isothiocyanato...
C7H5N4S
Molecular Mass 177.206 g·mol−1 Heat of Formation 577.7 ± 16.7 kJ·mol−1 Dipole Moment 1.74 ± 1.08 D Volume 200.77 Å 3 1-Azido-4-Isothiocyanato...
C7H5N4S
1-Azido-4-Isothiocyanato...
C7H5N4S
Molecular Mass 177.206 g·mol−1 Heat of Formation 577.3 ± 16.7 kJ·mol−1 Dipole Moment 1.52 ± 1.08 D Volume 201.39 Å 3 2-[(e)-(4-Hydroxy-3,5-Di...
C15H14N2O3
2-[(e)-(4-Hydroxy-3,5-Di...
C15H14N2O3
Molecular Mass 270.283 g·mol−1 Heat of Formation -222.6 ± 16.7 kJ·mol−1 Dipole Moment 1.00 ± 1.08 D Volume 318.57 Å 3 Methyl Red
C15H15N3O2
Methyl Red
C15H15N3O2
Molecular Mass 269.299 g·mol−1 Heat of Formation 35.3 ± 16.7 kJ·mol−1 Dipole Moment 3.03 ± 1.08 D Volume 319.88 Å 3 3-(2-Aminoethyl)-6-[2-(4...
C16H16N8O3
3-(2-Aminoethyl)-6-[2-(4...
C16H16N8O3
Molecular Mass 368.350 g·mol−1 Heat of Formation 731.7 ± 16.7 kJ·mol−1 Dipole Moment 7.25 ± 1.08 D Volume 409.13 Å 3 Methyl Phenylazoformate
C8H8N2O2
Methyl Phenylazoformate
C8H8N2O2
Molecular Mass 164.161 g·mol−1 Heat of Formation -36.2 ± 16.7 kJ·mol−1 Dipole Moment 2.61 ± 1.08 D Volume 191.5 Å 3 4-Azidophenol
C6H6N3O
4-Azidophenol
C6H6N3O
Molecular Mass 136.131 g·mol−1 Heat of Formation 234.4 ± 16.7 kJ·mol−1 Dipole Moment 3.56 ± 1.08 D Volume 157.06 Å 3 (6r)-5-Acetamido-2,6-Anh...
C17H20N5O9S
(6r)-5-Acetamido-2,6-Anh...
C17H20N5O9S
Molecular Mass 470.434 g·mol−1 Heat of Formation -832.9 ± 16.7 kJ·mol−1 Dipole Moment 6.02 ± 1.08 D Volume 497.59 Å 3 (6r)-5-Acetamido-2,6-Anh...
C17H20N5O9S
(6r)-5-Acetamido-2,6-Anh...
C17H20N5O9S
Molecular Mass 470.434 g·mol−1 Heat of Formation -833.8 ± 16.7 kJ·mol−1 Dipole Moment 5.81 ± 1.08 D Volume 496.58 Å 3 2-[(e)-(4-Hydroxy-3,5-Di...
C15H14N2O5
2-[(e)-(4-Hydroxy-3,5-Di...
C15H14N2O5
Molecular Mass 302.282 g·mol−1 Heat of Formation -448.1 ± 16.7 kJ·mol−1 Dipole Moment 3.17 ± 1.08 D Volume 339.61 Å 3 4-Azido-N-[2-[[(z)-N-Cya...
C26H33IN9O2
4-Azido-N-[2-[[(z)-N-Cya...
C26H33IN9O2
Molecular Mass 630.504 g·mol−1 Heat of Formation 405.0 ± 16.7 kJ·mol−1 Dipole Moment 7.62 ± 1.08 D Volume 685.69 Å 3 N-(4-Azido-2,3,5,6-Tetra...
C14H10F4N5O3
N-(4-Azido-2,3,5,6-Tetra...
C14H10F4N5O3
Molecular Mass 372.255 g·mol−1 Heat of Formation -731.7 ± 16.7 kJ·mol−1 Dipole Moment 3.25 ± 1.08 D Volume 375.98 Å 3 5-Azidoisophthalic Acid
C8H6N3O4
5-Azidoisophthalic Acid
C8H6N3O4
Molecular Mass 208.151 g·mol−1 Heat of Formation -313.3 ± 16.7 kJ·mol−1 Dipole Moment 1.59 ± 1.08 D Volume 219.39 Å 3 1-({(6r,7r)-2-Carboxy-8-...
C27H27N6O4S2+
1-({(6r,7r)-2-Carboxy-8-...
C27H27N6O4S2+
Molecular Mass 563.671 g·mol−1 Heat of Formation 198.1 ± 16.7 kJ·mol−1 Dipole Moment 7.82 ± 1.08 D Volume 636.98 Å 3 Ethyl (1z)-2-[(4-Azidobe...
C11H14N5O2
Ethyl (1z)-2-[(4-Azidobe...
C11H14N5O2
Molecular Mass 248.261 g·mol−1 Heat of Formation 104.3 ± 16.7 kJ·mol−1 Dipole Moment 1.00 ± 1.08 D Volume 296.37 Å 3 2-Azido-N-(2-Sulfanyleth...
C4H9N4OS
2-Azido-N-(2-Sulfanyleth...
C4H9N4OS
Molecular Mass 161.205 g·mol−1 Heat of Formation 117.9 ± 16.7 kJ·mol−1 Dipole Moment 3.54 ± 1.08 D Volume 191.01 Å 3 N-[2-(4-Azido-3-Iodophen...
C21H12IN5O4
N-[2-(4-Azido-3-Iodophen...
C21H12IN5O4
Molecular Mass 525.256 g·mol−1 Heat of Formation 2849.3 ± 16.7 kJ·mol−1 Dipole Moment 7.45 ± 1.08 D Volume 482.49 Å 3 (3-Azido-4-Chloro-Phenyl...
C7H7ClN5S
(3-Azido-4-Chloro-Phenyl...
C7H7ClN5S
Molecular Mass 228.682 g·mol−1 Heat of Formation 437.0 ± 16.7 kJ·mol−1 Dipole Moment 4.19 ± 1.08 D Volume 242.09 Å 3 2-[(4-Azido-2-Nitropheny...
C8H10N7O3
2-[(4-Azido-2-Nitropheny...
C8H10N7O3
Molecular Mass 252.210 g·mol−1 Heat of Formation 319.2 ± 16.7 kJ·mol−1 Dipole Moment 7.75 ± 1.08 D Volume 271.42 Å 3 4-(4-Chlorophenyl)-1-[4-...
C28H31ClFN4O3
4-(4-Chlorophenyl)-1-[4-...
C28H31ClFN4O3
Molecular Mass 526.022 g·mol−1 Heat of Formation 859.2 ± 16.7 kJ·mol−1 Dipole Moment 4.62 ± 1.08 D Volume 587.38 Å 3 Imino-[(2,3,5,6-Tetraflu...
C5H2F4N4
Imino-[(2,3,5,6-Tetraflu...
C5H2F4N4
Molecular Mass 194.090 g·mol−1 Heat of Formation -216.8 ± 16.7 kJ·mol−1 Dipole Moment 1.34 ± 1.08 D Volume 175.17 Å 3 4-[(4-Azido-2-Nitropheny...
C29H24N7O5
4-[(4-Azido-2-Nitropheny...
C29H24N7O5
Molecular Mass 550.545 g·mol−1 Heat of Formation 4191.3 ± 16.7 kJ·mol−1 Dipole Moment 3.78 ± 1.08 D Volume 598.46 Å 3 4-Azidobenzaldehyde
C7H6N3O
4-Azidobenzaldehyde
C7H6N3O
Molecular Mass 148.142 g·mol−1 Heat of Formation 292.5 ± 16.7 kJ·mol−1 Dipole Moment 2.58 ± 1.08 D Volume 173.25 Å 3 Methyl 4-Azidobenzenecar...
C8H9N4O
Methyl 4-Azidobenzenecar...
C8H9N4O
Molecular Mass 177.183 g·mol−1 Heat of Formation 314.5 ± 16.7 kJ·mol−1 Dipole Moment 2.92 ± 1.08 D Volume 211.64 Å 3 N-(4-Azido-2,3,5,6-Tetra...
C17H16F4N5O3
N-(4-Azido-2,3,5,6-Tetra...
C17H16F4N5O3
Molecular Mass 414.334 g·mol−1 Heat of Formation -805.0 ± 16.7 kJ·mol−1 Dipole Moment 5.90 ± 1.08 D Volume 439.63 Å 3 3-Azidopyridin-1-Ium-3-I...
C5H6N4
3-Azidopyridin-1-Ium-3-I...
C5H6N4
Molecular Mass 122.128 g·mol−1 Heat of Formation 459.5 ± 16.7 kJ·mol−1 Dipole Moment 2.72 ± 1.08 D Volume 140.68 Å 3 (e)-7-[(1s,2s,3s,5r)-3-[...
C22H30IN4O4S
(e)-7-[(1s,2s,3s,5r)-3-[...
C22H30IN4O4S
Molecular Mass 573.467 g·mol−1 Heat of Formation -280.6 ± 16.7 kJ·mol−1 Dipole Moment 5.71 ± 1.08 D Volume 572.48 Å 3 (e)-7-[(1s,2r,3r,5r)-3-[...
C22H30IN4O4S
(e)-7-[(1s,2r,3r,5r)-3-[...
C22H30IN4O4S
Molecular Mass 573.467 g·mol−1 Heat of Formation -262.2 ± 16.7 kJ·mol−1 Dipole Moment 2.77 ± 1.08 D Volume 583.87 Å 3 2-Azido-4-Nitrophenol
C6H5N4O3
2-Azido-4-Nitrophenol
C6H5N4O3
Molecular Mass 181.129 g·mol−1 Heat of Formation 215.3 ± 16.7 kJ·mol−1 Dipole Moment 5.59 ± 1.08 D Volume 187.93 Å 3 [[(2r,3s,4r,5r)-5-(6-Ami...
C21H29N10O14P2
[[(2r,3s,4r,5r)-5-(6-Ami...
C21H29N10O14P2
Molecular Mass 707.461 g·mol−1 Heat of Formation -2366.7 ± 16.7 kJ·mol−1 Dipole Moment 9.67 ± 1.08 D Volume 682.81 Å 3 1-(3-Azido-2,3-Dideoxy-5...
C30H16N5O7
1-(3-Azido-2,3-Dideoxy-5...
C30H16N5O7
Molecular Mass 558.477 g·mol−1 Heat of Formation 2753.8 ± 16.7 kJ·mol−1 Dipole Moment 9.32 ± 1.08 D Volume 576.27 Å 3 3'-Azido-2',3'-Dideoxy-5...
C16H19N6O5
3'-Azido-2',3'-Dideoxy-5...
C16H19N6O5
Molecular Mass 375.359 g·mol−1 Heat of Formation -413.0 ± 16.7 kJ·mol−1 Dipole Moment 6.56 ± 1.08 D Volume 420.12 Å 3 3'-Azido-2',3'-Dideoxy-5...
C16H19N6O5++
3'-Azido-2',3'-Dideoxy-5...
C16H19N6O5++
Molecular Mass 375.359 g·mol−1 Heat of Formation -413.9 ± 16.7 kJ·mol−1 Dipole Moment 4.88 ± 1.08 D Volume 422.63 Å 3 2-[(4-Azidobenzoyl)amino...
C10H12N5O2
2-[(4-Azidobenzoyl)amino...
C10H12N5O2
Molecular Mass 234.235 g·mol−1 Heat of Formation 239.1 ± 16.7 kJ·mol−1 Dipole Moment 3.47 ± 1.08 D Volume 271.92 Å 3 2-Azido-N-Benzyl-7h-Puri...
C12H12N8
2-Azido-N-Benzyl-7h-Puri...
C12H12N8
Molecular Mass 268.277 g·mol−1 Heat of Formation 758.7 ± 16.7 kJ·mol−1 Dipole Moment 9.37 ± 1.08 D Volume 301.81 Å 3 6-Azido-3-[2-[4-(4-Fluor...
C22H22FN6O3
6-Azido-3-[2-[4-(4-Fluor...
C22H22FN6O3
Molecular Mass 437.447 g·mol−1 Heat of Formation -184.9 ± 16.7 kJ·mol−1 Dipole Moment 1.58 ± 1.08 D Volume 495.88 Å 3 (e)-7-[(1s,2r,3r,5r)-3-[...
C25H35IN4O3
(e)-7-[(1s,2r,3r,5r)-3-[...
C25H35IN4O3
Molecular Mass 566.475 g·mol−1 Heat of Formation -181.4 ± 16.7 kJ·mol−1 Dipole Moment 6.50 ± 1.08 D Volume 607.36 Å 3 4-[(4-Azido-2-Nitro-Anil...
C14H16N6O4
4-[(4-Azido-2-Nitro-Anil...
C14H16N6O4
Molecular Mass 332.315 g·mol−1 Heat of Formation 99.8 ± 16.7 kJ·mol−1 Dipole Moment 7.17 ± 1.08 D Volume 362.28 Å 3 3-[3-(4-Azidophenyl)sulf...
C29H30IN4O5S
3-[3-(4-Azidophenyl)sulf...
C29H30IN4O5S
Molecular Mass 673.542 g·mol−1 Heat of Formation -320.6 ± 16.7 kJ·mol−1 Dipole Moment 9.48 ± 1.08 D Volume 692.34 Å 3 3-{3-[(4-Azidophenyl)sul...
C29H30IN4O5S
3-{3-[(4-Azidophenyl)sul...
C29H30IN4O5S
Molecular Mass 673.542 g·mol−1 Heat of Formation -320.6 ± 16.7 kJ·mol−1 Dipole Moment 9.48 ± 1.08 D Volume 692.54 Å 3 (5r)-5-(4-Azidophenyl)-8...
C17H18IN4O
(5r)-5-(4-Azidophenyl)-8...
C17H18IN4O
Molecular Mass 421.255 g·mol−1 Heat of Formation 392.4 ± 16.7 kJ·mol−1 Dipole Moment 3.91 ± 1.08 D Volume 395.52 Å 3 N-(4-Azidobenzoyl)glycyl...
C15H21N6O4
N-(4-Azidobenzoyl)glycyl...
C15H21N6O4
Molecular Mass 349.365 g·mol−1 Heat of Formation -365.2 ± 16.7 kJ·mol−1 Dipole Moment 3.13 ± 1.08 D Volume 416.83 Å 3 2-Azidoethanol
C2H6N3O
2-Azidoethanol
C2H6N3O
Molecular Mass 88.089 g·mol−1 Heat of Formation 99.0 ± 16.7 kJ·mol−1 Dipole Moment 1.91 ± 1.08 D Volume 107.13 Å 3 4-[(1s,3s)-3-[2-(4-Azido...
C31H36FN6O
4-[(1s,3s)-3-[2-(4-Azido...
C31H36FN6O
Molecular Mass 527.655 g·mol−1 Heat of Formation 244.6 ± 16.7 kJ·mol−1 Dipole Moment 5.08 ± 1.08 D Volume 649.88 Å 3 4-Azido-2-Methoxy-5-(met...
C17H27N6O4S
4-Azido-2-Methoxy-5-(met...
C17H27N6O4S
Molecular Mass 411.499 g·mol−1 Heat of Formation -328.0 ± 16.7 kJ·mol−1 Dipole Moment 1.79 ± 1.08 D Volume 480.78 Å 3 4-Azido-N-[(1r,2r,3r,4r)...
C13H17N4O7
4-Azido-N-[(1r,2r,3r,4r)...
C13H17N4O7
Molecular Mass 341.297 g·mol−1 Heat of Formation -856.0 ± 16.7 kJ·mol−1 Dipole Moment 4.87 ± 1.08 D Volume 383.0 Å 3 2-Azido-N-[(1r,2r)-2-Hyd...
C11H14N5O5
2-Azido-N-[(1r,2r)-2-Hyd...
C11H14N5O5
Molecular Mass 296.259 g·mol−1 Heat of Formation -195.1 ± 16.7 kJ·mol−1 Dipole Moment 6.64 ± 1.08 D Volume 325.9 Å 3 3,3'-Azobis(benzeneaceti...
C16H14N2O4
3,3'-Azobis(benzeneaceti...
C16H14N2O4
Molecular Mass 298.293 g·mol−1 Heat of Formation -402.3 ± 16.7 kJ·mol−1 Dipole Moment 0.63 ± 1.08 D Volume 345.66 Å 3 1-Azido-5-Isothiocyanato...
C11H7N4S
1-Azido-5-Isothiocyanato...
C11H7N4S
Molecular Mass 227.265 g·mol−1 Heat of Formation 661.5 ± 16.7 kJ·mol−1 Dipole Moment 0.76 ± 1.08 D Volume 256.64 Å 3 1-Azido-5-Isothiocyanato...
C11H7N4S
1-Azido-5-Isothiocyanato...
C11H7N4S
Molecular Mass 227.265 g·mol−1 Heat of Formation 662.0 ± 16.7 kJ·mol−1 Dipole Moment 0.72 ± 1.08 D Volume 256.37 Å 3 1-[2-(4-Azido-3-Iodophen...
C19H20F3IN5
1-[2-(4-Azido-3-Iodophen...
C19H20F3IN5
Molecular Mass 502.295 g·mol−1 Heat of Formation -49.5 ± 16.7 kJ·mol−1 Dipole Moment 3.70 ± 1.08 D Volume 471.52 Å 3 (2s,4s)-4-[[2-(4-Azidoph...
C18H15Cl2N5O3
(2s,4s)-4-[[2-(4-Azidoph...
C18H15Cl2N5O3
Molecular Mass 420.249 g·mol−1 Heat of Formation -165.3 ± 16.7 kJ·mol−1 Dipole Moment 3.91 ± 1.08 D Volume 457.51 Å 3 (3r,4ar,5s,6s,6as,10s,10...
C32H45IN5O8
(3r,4ar,5s,6s,6as,10s,10...
C32H45IN5O8
Molecular Mass 754.633 g·mol−1 Heat of Formation -1070.4 ± 16.7 kJ·mol−1 Dipole Moment 1.83 ± 1.08 D Volume 781.89 Å 3 (2s,4s,5r,6r)-5-Acetamid...
C17H22N5O10S
(2s,4s,5r,6r)-5-Acetamid...
C17H22N5O10S
Molecular Mass 488.449 g·mol−1 Heat of Formation -1134.6 ± 16.7 kJ·mol−1 Dipole Moment 8.65 ± 1.08 D Volume 513.96 Å 3 4-Azido-2-Hydroxy-N-{4-[...
C13H17IN5O3
4-Azido-2-Hydroxy-N-{4-[...
C13H17IN5O3
Molecular Mass 418.210 g·mol−1 Heat of Formation -121.3 ± 16.7 kJ·mol−1 Dipole Moment 7.32 ± 1.08 D Volume 392.19 Å 3 [4-(4-Chlorophenyl)-1-[4...
C28H27ClFN4O3
[4-(4-Chlorophenyl)-1-[4...
C28H27ClFN4O3
Molecular Mass 521.990 g·mol−1 Heat of Formation -164.0 ± 16.7 kJ·mol−1 Dipole Moment 2.98 ± 1.08 D Volume 605.81 Å 3 Methyl N-(4-((2-Chloro-4...
C19H18ClN5O4
Methyl N-(4-((2-Chloro-4...
C19H18ClN5O4
Molecular Mass 415.830 g·mol−1 Heat of Formation 97.7 ± 16.7 kJ·mol−1 Dipole Moment 4.69 ± 1.08 D Volume 476.25 Å 3 (3s,4r,4ar,7r,7ar,12bs)-...
C17H21N4O2
(3s,4r,4ar,7r,7ar,12bs)-...
C17H21N4O2
Molecular Mass 313.374 g·mol−1 Heat of Formation 68.2 ± 16.7 kJ·mol−1 Dipole Moment 4.80 ± 1.08 D Volume 363.36 Å 3 [(3r,4as,5r,6r,6ar,10r,1...
C32H44IN4O8
[(3r,4as,5r,6r,6ar,10r,1...
C32H44IN4O8
Molecular Mass 739.618 g·mol−1 Heat of Formation -1140.7 ± 16.7 kJ·mol−1 Dipole Moment 5.53 ± 1.08 D Volume 758.99 Å 3 L-Leucyl-L-Leucyl-4-Azid...
C21H32N7O6
L-Leucyl-L-Leucyl-4-Azid...
C21H32N7O6
Molecular Mass 478.522 g·mol−1 Heat of Formation -539.1 ± 16.7 kJ·mol−1 Dipole Moment 3.23 ± 1.08 D Volume 588.41 Å 3 Azulfidine
C18H14N4O5S
Azulfidine
C18H14N4O5S
Molecular Mass 398.393 g·mol−1 Heat of Formation -381.0 ± 16.7 kJ·mol−1 Dipole Moment 4.27 ± 1.08 D Volume 424.06 Å 3 2,5-Dioxo-1-Pyrrolidinyl...
C13H12N5O5
2,5-Dioxo-1-Pyrrolidinyl...
C13H12N5O5
Molecular Mass 318.265 g·mol−1 Heat of Formation -276.4 ± 16.7 kJ·mol−1 Dipole Moment 4.16 ± 1.08 D Volume 347.45 Å 3 (2,5-Dioxopyrrolidin-1-Y...
C13H12N5O5
(2,5-Dioxopyrrolidin-1-Y...
C13H12N5O5
Molecular Mass 318.265 g·mol−1 Heat of Formation -277.4 ± 16.7 kJ·mol−1 Dipole Moment 4.57 ± 1.08 D Volume 347.47 Å 3 N-[2-(4-Azido-3-Iodophen...
C21H27IN5O4
N-[2-(4-Azido-3-Iodophen...
C21H27IN5O4
Molecular Mass 540.375 g·mol−1 Heat of Formation -232.0 ± 16.7 kJ·mol−1 Dipole Moment 3.79 ± 1.08 D Volume 545.22 Å 3 (4s)-N-[2-(4-Azido-3-Iod...
C21H27IN5O4
(4s)-N-[2-(4-Azido-3-Iod...
C21H27IN5O4
Molecular Mass 540.375 g·mol−1 Heat of Formation -260.9 ± 16.7 kJ·mol−1 Dipole Moment 3.27 ± 1.08 D Volume 548.56 Å 3 (4e)-2-Methyl-4-({4-[(e)...
C19H16N4O
(4e)-2-Methyl-4-({4-[(e)...
C19H16N4O
Molecular Mass 316.357 g·mol−1 Heat of Formation 510.7 ± 16.7 kJ·mol−1 Dipole Moment 3.46 ± 1.08 D Volume 376.34 Å 3 3-Azido-4-[(e)-2-(1,1,4,...
C24H28N3O2
3-Azido-4-[(e)-2-(1,1,4,...
C24H28N3O2
Molecular Mass 390.498 g·mol−1 Heat of Formation -20.6 ± 16.7 kJ·mol−1 Dipole Moment 4.50 ± 1.08 D Volume 493.46 Å 3 4,4′-Azodibenzoic Acid
C14H10N2O4
4,4′-Azodibenzoic Acid
C14H10N2O4
Molecular Mass 270.240 g·mol−1 Heat of Formation -336.0 ± 16.7 kJ·mol−1 Dipole Moment 2.37 ± 1.08 D Volume 304.11 Å 3 1-[5-Azido-2-[(2r)-2-Hyd...
C14H21N4O3
1-[5-Azido-2-[(2r)-2-Hyd...
C14H21N4O3
Molecular Mass 293.341 g·mol−1 Heat of Formation -182.1 ± 16.7 kJ·mol−1 Dipole Moment 3.82 ± 1.08 D Volume 365.45 Å 3 [(4z)-5-Hydroxy-4-{[(e)-...
C14H26N4O6P+
[(4z)-5-Hydroxy-4-{[(e)-...
C14H26N4O6P+
Molecular Mass 377.353 g·mol−1 Heat of Formation -880.3 ± 16.7 kJ·mol−1 Dipole Moment 11.40 ± 1.08 D Volume 391.8 Å 3 2-Amino-6-Azido-1-Hexano...
C6H3N4O
2-Amino-6-Azido-1-Hexano...
C6H3N4O
Molecular Mass 147.114 g·mol−1 Heat of Formation 862.0 ± 16.7 kJ·mol−1 Dipole Moment 4.87 ± 1.08 D Volume 182.94 Å 3 Trans-Methyl-Ethyl-Diaze...
C3H8N2
Trans-Methyl-Ethyl-Diaze...
C3H8N2
Molecular Mass 72.109 g·mol−1 Heat of Formation 102.5 ± 16.7 kJ·mol−1 Dipole Moment 0.26 ± 1.08 D Volume 105.75 Å 3 1-Ethyl-2-Methyldiazene
C3H8N2
1-Ethyl-2-Methyldiazene
C3H8N2
Molecular Mass 72.109 g·mol−1 Heat of Formation 102.5 ± 16.7 kJ·mol−1 Dipole Moment 0.26 ± 1.08 D Volume 105.75 Å 3 [(3s)-3-[[(1r)-2-Amino-1...
C15H17N6O6S2
[(3s)-3-[[(1r)-2-Amino-1...
C15H17N6O6S2
Molecular Mass 441.462 g·mol−1 Heat of Formation -141.2 ± 16.7 kJ·mol−1 Dipole Moment 3.22 ± 1.08 D Volume 474.94 Å 3 2-[4-[3-[7-Azido-2-(trif...
C22H25F3N6OS
2-[4-[3-[7-Azido-2-(trif...
C22H25F3N6OS
Molecular Mass 478.534 g·mol−1 Heat of Formation -283.8 ± 16.7 kJ·mol−1 Dipole Moment 4.15 ± 1.08 D Volume 542.52 Å 3 [(3r,4as,5r,6r,6ar,10r,1...
C33H44IN5O10
[(3r,4as,5r,6r,6ar,10r,1...
C33H44IN5O10
Molecular Mass 797.634 g·mol−1 Heat of Formation -1474.0 ± 16.7 kJ·mol−1 Dipole Moment 5.51 ± 1.08 D Volume 805.61 Å 3 1-[4-(4-Amino-6,7-Dimeth...
C25H31IN8O3
1-[4-(4-Amino-6,7-Dimeth...
C25H31IN8O3
Molecular Mass 618.470 g·mol−1 Heat of Formation 156.2 ± 16.7 kJ·mol−1 Dipole Moment 0.64 ± 1.08 D Volume 631.78 Å 3 N'-(4-Azido-2-Nitro-Phen...
C8H11N6O2
N'-(4-Azido-2-Nitro-Phen...
C8H11N6O2
Molecular Mass 223.212 g·mol−1 Heat of Formation 393.9 ± 16.7 kJ·mol−1 Dipole Moment 7.22 ± 1.08 D Volume 250.64 Å 3 3-Methylbenzyl Azide
C8H10N3
3-Methylbenzyl Azide
C8H10N3
Molecular Mass 148.185 g·mol−1 Heat of Formation 354.4 ± 16.7 kJ·mol−1 Dipole Moment 3.17 ± 1.08 D Volume 189.48 Å 3 (2e)-8-Amino-7-[(e)-(4-N...
C22H16N6O3
(2e)-8-Amino-7-[(e)-(4-N...
C22H16N6O3
Molecular Mass 412.401 g·mol−1 Heat of Formation 535.1 ± 16.7 kJ·mol−1 Dipole Moment 11.04 ± 1.08 D Volume 456.51 Å 3 (2e)-8-Amino-7-[(e)-(4-N...
C22H16N6O3
(2e)-8-Amino-7-[(e)-(4-N...
C22H16N6O3
Molecular Mass 412.401 g·mol−1 Heat of Formation 541.0 ± 16.7 kJ·mol−1 Dipole Moment 10.06 ± 1.08 D Volume 455.24 Å 3