Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H12N2 |
| Molecular Weight | 184.2371 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N(NC1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=YBQZXXMEJHZYMB-UHFFFAOYSA-N
InChI=1S/C12H12N2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10,13-14H
| Molecular Formula | C12H12N2 |
| Molecular Weight | 184.2371 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Preparation and properties of a monomeric Mn(IV)-oxo complex. | 2006 Jul 12 |
|
| Tuning the electronic properties of cyclopentadienyl analogs with CB2N2 frameworks: 1,2-diphenyl-1,2-diaza-3,5-diborolyl ligands and their alkali metal salts. | 2008 Jul 14 |
|
| Characterisation of hydrazides and hydrazine derivatives as novel aspartic protease inhibitors. | 2010 Oct |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:37:12 GMT 2023
by
admin
on
Fri Dec 15 17:37:12 GMT 2023
|
| Record UNII |
1G3CS09TUK
|
| Record Status |
Validated (UNII)
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| Record Version |
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Common Name | English | ||
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Common Name | English |
| Code System | Code | Type | Description | ||
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C44392
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122-66-7
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Hydrazobenzene
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admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
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1G3CS09TUK
Created by
admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
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DTXSID7020710
Created by
admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
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2882
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204-563-5
Created by
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3510
Created by
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31222
Created by
admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
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C032041
Created by
admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> IMPURITY |
For the calculation of contents, multiply the peak areas by 0.55
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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