4-(4-NITROBENZYL)PYRIDINE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C12H10N2O2
Molecular Weight	214.22
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

[O-][N+](=O)C1=CC=C(CC2=CC=NC=C2)C=C1

InChI

InChIKey=MNHKUCBXXMFQDM-UHFFFAOYSA-N

InChI=1S/C12H10N2O2/c15-14(16)12-3-1-10(2-4-12)9-11-5-7-13-8-6-11/h1-8H,9H2

HIDE SMILES / InChI

Molecular Formula	C12H10N2O2
Molecular Weight	214.22
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
4-Amino-benzoic acid-4,4'-(propane-1,3-diyl)dipyridine (1/1).	2010-10-09	21588953
Alkylating potential of oxetanes.	2010-07-19	20550097
4-Amino-benzoic acid-1,2-bis-(4-pyrid-yl)ethane (2/1).	2010-06-05	21587796
4-(4-Nitro-benz-yl)pyridinium 5-nitro-salicylate.	2010-04-24	21579214
Reactivity of the mutagen 1,4-dinitro-2-methylpyrrole as an alkylating agent.	2010-03-05	20121054
Sorbate-nitrite interactions: acetonitrile oxide as an alkylating agent.	2009-07	19580248
Decreased susceptibility of the cytochrome P450 2B6 variant K262R to inhibition by several clinically important drugs.	2009-03	19074527
Evaluation of fluoren-NU as a novel antitumor agent.	2009	19718945
Chemical reactivity and biological activity of diketene.	2008-10	18759502
Synthesis, spectroscopy and alkylating properties of Pd(II) complexes of phosphorohydrazones of coumarin and chromone with potential antibacterial activity.	2008-06-11	18540163
Abstracts of papers presented at the 2008 pittsburgh conference.	2008	19365566
Genotoxicity profiles of common alkyl halides and esters with alkylating activity.	2007-10-04	17644026
New potent and selective cytochrome P450 2B6 (CYP2B6) inhibitors based on three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis.	2007-04	17325652
In vitro induction of micronuclei by monofunctional methanesulphonic acid esters: possible role of alkylation mechanisms.	2006-12-01	17011536
Autoxidative activation of the nematocide 1,3-dichloropropene to highly genotoxic and mutagenic derivatives: consideration of genotoxic/carcinogenic mechanisms.	2006-07	16841964
Alkylating potential of potassium sorbate.	2005-12-28	16366722
Evaluation of fluorenhymustine as a rationally designed novel anticancer agent.	2005-12	16404347
Colorimetric assays for quantitative analysis and screening of epoxide hydrolase activity.	2005-12	16328991
Nitrosation of glycine ethyl ester and ethyl diazoacetate to give the alkylating agent and mutagen ethyl chloro(hydroximino)acetate.	2004-03	15025513
Colorimetric high-throughput assay for alkene epoxidation catalyzed by cytochrome P450 BM-3 variant 139-3.	2004-03	15006137
Alkylating reactivity and herbicidal activity of chloroacetamides.	2003-04	12701706
On-resin real-time reaction monitoring of solid-phase oligosaccharide synthesis.	2002-10-30	12392392
Mutagenicity of bisphenol A (4,4'-isopropylidenediphenol) in vitro: effects of nitrosylation.	2002	12395404
Synthesis, antimicrobial, and alkylating properties of 3-phosphonic derivatives of chromone.	2001-12	11852533
Metabolic activation of mitomycin C by NADPH-ferredoxin reductase in vitro.	2001-02-23	11263680

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:24:17 GMT 2025` Edited by `admin` on `Mon Mar 31 19:24:17 GMT 2025`
Record UNII	0Z6GS37N7H
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NSC-83591

Preferred Name

English

4-(4-NITROBENZYL)PYRIDINE

Systematic Name

English

PYRIDINE, 4-((4-NITROPHENYL)METHYL)-

Systematic Name

English

4-(P-NITROBENZYL)PYRIDINE

Common Name

English

PYRIDINE, 4-(P-NITROBENZYL)

Common Name

English

.GAMMA.-(4-NITROBENZYL)PYRIDINE

Common Name

English

4-((4-NITROPHENYL)METHYL)PYRIDINE

Systematic Name

English

.GAMMA.-(P-NITROBENZYL)PYRIDINE

Common Name

English

4-(4'-NITROBENZYL)PYRIDINE

Common Name

English

Code System Code Type Description

EPA CompTox

DTXSID2061482