Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H10N2O |
| Molecular Weight | 198.2206 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=NN(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=UBUCNCOMADRQHX-UHFFFAOYSA-N
InChI=1S/C12H10N2O/c15-13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
| Molecular Formula | C12H10N2O |
| Molecular Weight | 198.2206 |
| 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 |
|---|---|---|
| Transformation of BALB/c-3T3 cells: IV. Rank-ordered potency of 24 chemical responses detected in a sensitive new assay procedure. | 1993 Jul |
|
| Genotoxic effects of N-nitrosodicyclohexylamine in isolated human lymphocytes. | 2001 Apr |
|
| Determination of N-nitrosodimethylamine in artificial gastric juice by gas chromatography-mass spectrometry and by gas chromatography-thermal energy analysis. | 2001 Jun |
|
| Mechanistic studies of N-nitrosodimethylamine (NDMA) formation in chlorinated drinking water. | 2002 Apr |
|
| Formation of N-nitrosodimethylamine (NDMA) from reaction of monochloramine: a new disinfection by-product. | 2002 Feb |
|
| A quantitative comparison of smokeless measurements. | 2002 Nov |
|
| A qualitative comparison of smokeless powder measurements. | 2002 Sep |
|
| Assessment of the performance of the Ames II assay: a collaborative study with 19 coded compounds. | 2004 Mar 14 |
|
| Evaluation of the ability of a battery of three in vitro genotoxicity tests to discriminate rodent carcinogens and non-carcinogens I. Sensitivity, specificity and relative predictivity. | 2005 Jul 4 |
|
| Inhibitory effect of yuzu essential oil on the formation of N-nitrosodimethylamine in vegetables. | 2005 May 18 |
|
| Occurrence of N-nitrosodimethylamine in South Korean and imported alcoholic beverages. | 2005 Nov |
|
| Relationship of superficial scald development and alpha-farnesene oxidation to reactions of diphenylamine and diphenylamine derivatives in Cv. Granny Smith apple peel. | 2005 Oct 19 |
|
| Oxidative remediation of diphenylamine in wastewater. | 2006 Apr |
|
| Characterization of new nitrosamines in drinking water using liquid chromatography tandem mass spectrometry. | 2006 Dec 15 |
|
| Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006 Nov |
|
| Development of a quantitative LC-MS/MS method for the analysis of common propellant powder stabilizers in gunshot residue. | 2007 Jul |
|
| Mechanistic aspects of the oxidative and reductive fragmentation of N-nitrosoamines: a new method for generating nitrenium cations, amide anions, and aminyl radicals. | 2007 Mar 21 |
|
| Formation of N-nitrosamines from eleven disinfection treatments of seven different surface waters. | 2008 Jul 1 |
|
| A cell-microelectronic sensing technique for profiling cytotoxicity of chemicals. | 2008 May 12 |
|
| Diphenylamine metabolism in 'braeburn' apples stored under conditions conducive to the development of internal browning. | 2008 May 14 |
|
| Formation of N-nitrosodiphenylamine and two new N-containing disinfection byproducts from chloramination of water containing diphenylamine. | 2009 Nov 1 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:21:34 GMT 2023
by
admin
on
Sat Dec 16 01:21:34 GMT 2023
|
| Record UNII |
AP2V89J1DA
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Brand Name | English | ||
|
Systematic Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
C023649
Created by
admin on Sat Dec 16 01:21:34 GMT 2023 , Edited by admin on Sat Dec 16 01:21:34 GMT 2023
|
PRIMARY | |||
|
86-30-6
Created by
admin on Sat Dec 16 01:21:34 GMT 2023 , Edited by admin on Sat Dec 16 01:21:34 GMT 2023
|
PRIMARY | |||
|
585
Created by
admin on Sat Dec 16 01:21:34 GMT 2023 , Edited by admin on Sat Dec 16 01:21:34 GMT 2023
|
PRIMARY | |||
|
2875
Created by
admin on Sat Dec 16 01:21:34 GMT 2023 , Edited by admin on Sat Dec 16 01:21:34 GMT 2023
|
PRIMARY | |||
|
AP2V89J1DA
Created by
admin on Sat Dec 16 01:21:34 GMT 2023 , Edited by admin on Sat Dec 16 01:21:34 GMT 2023
|
PRIMARY | |||
|
DTXSID6021030
Created by
admin on Sat Dec 16 01:21:34 GMT 2023 , Edited by admin on Sat Dec 16 01:21:34 GMT 2023
|
PRIMARY | |||
|
201-663-0
Created by
admin on Sat Dec 16 01:21:34 GMT 2023 , Edited by admin on Sat Dec 16 01:21:34 GMT 2023
|
PRIMARY | |||
|
6838
Created by
admin on Sat Dec 16 01:21:34 GMT 2023 , Edited by admin on Sat Dec 16 01:21:34 GMT 2023
|
PRIMARY |