Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H10N2O |
| Molecular Weight | 198.2206 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C(C=C1)\N=N\C2=CC=CC=C2
InChI
InChIKey=BEYOBVMPDRKTNR-BUHFOSPRSA-N
InChI=1S/C12H10N2O/c15-12-8-6-11(7-9-12)14-13-10-4-2-1-3-5-10/h1-9,15H/b14-13+
| Molecular Formula | C12H10N2O |
| Molecular Weight | 198.2206 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Selective and direct immobilization of cysteinyl biomolecules by electrochemical cleavage of azo linkage. | 2010-10-05 |
|
| Synthesis of diaryl-azo derivatives as potential antifungal agents. | 2010-07-15 |
|
| Gas-phase tautomerism in hydroxy azo dyes - from 4-phenylazo-1-phenol to 4-phenylazo-anthracen-1-ol. | 2010-03 |
|
| Biotinylated glyco-functionalized quantum dots: synthesis, characterization, and cytotoxicity studies. | 2009-05-20 |
|
| 4-Chloro-2-[(E)-(4-nitro-phen-yl)diazenyl]phenol. | 2009-02-11 |
|
| Mycotoxin detection plays "cops and robbers": cyclodextrin chemosensors as specialized police? | 2008-12 |
|
| (E)-2-(5,5-Dimethyl-hexa-hydro-pyrimidin-2-yl)-4-(phenyl-diazen-yl)phenol. | 2008-11-26 |
|
| Density functional theory characterisation of 4-hydroxyazobenzene. | 2007-12 |
|
| Host-guest complexation affected by pH and length of spacer for hydroxyazobenzene-modified cyclodextrins. | 2006-12-21 |
|
| Assembly behavior of inclusion complexes of beta-cyclodextrin with 4-hydroxyazobenzene and 4-aminoazobenzene. | 2005-02-21 |
|
| Immature rat uterotrophic assay of 18 chemicals and Hershberger assay of 30 chemicals. | 2003-02-01 |
|
| Direct spectrophotometric assay of monooxygenase and oxidase activities of mushroom tyrosinase in the presence of synthetic and natural substrates. | 2003-01-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:45:52 GMT 2025
by
admin
on
Mon Mar 31 18:45:52 GMT 2025
|
| Record UNII |
VX4306NSH1
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
216-880-6
Created by
admin on Mon Mar 31 18:45:52 GMT 2025 , Edited by admin on Mon Mar 31 18:45:52 GMT 2025
|
PRIMARY | |||
|
VX4306NSH1
Created by
admin on Mon Mar 31 18:45:52 GMT 2025 , Edited by admin on Mon Mar 31 18:45:52 GMT 2025
|
PRIMARY | |||
|
5527
Created by
admin on Mon Mar 31 18:45:52 GMT 2025 , Edited by admin on Mon Mar 31 18:45:52 GMT 2025
|
PRIMARY | |||
|
Solvent Yellow 7
Created by
admin on Mon Mar 31 18:45:52 GMT 2025 , Edited by admin on Mon Mar 31 18:45:52 GMT 2025
|
PRIMARY | |||
|
DTXSID3022160
Created by
admin on Mon Mar 31 18:45:52 GMT 2025 , Edited by admin on Mon Mar 31 18:45:52 GMT 2025
|
PRIMARY | |||
|
3177
Created by
admin on Mon Mar 31 18:45:52 GMT 2025 , Edited by admin on Mon Mar 31 18:45:52 GMT 2025
|
PRIMARY | |||
|
1689-82-3
Created by
admin on Mon Mar 31 18:45:52 GMT 2025 , Edited by admin on Mon Mar 31 18:45:52 GMT 2025
|
PRIMARY |