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
Synthesis, antimicrobial, and alkylating properties of 3-phosphonic derivatives of chromone.	2001 Dec	11852533
Metabolic activation of mitomycin C by NADPH-ferredoxin reductase in vitro.	2001 Feb 23	11263680
Mutagenicity of bisphenol A (4,4'-isopropylidenediphenol) in vitro: effects of nitrosylation.	2002	12395404
On-resin real-time reaction monitoring of solid-phase oligosaccharide synthesis.	2002 Oct 30	12392392
Alkylating reactivity and herbicidal activity of chloroacetamides.	2003 Apr	12701706
Nitrosation of glycine ethyl ester and ethyl diazoacetate to give the alkylating agent and mutagen ethyl chloro(hydroximino)acetate.	2004 Mar	15025513
Colorimetric high-throughput assay for alkene epoxidation catalyzed by cytochrome P450 BM-3 variant 139-3.	2004 Mar	15006137
Colorimetric assays for quantitative analysis and screening of epoxide hydrolase activity.	2005 Dec	16328991
Alkylating potential of potassium sorbate.	2005 Dec 28	16366722
In vitro induction of micronuclei by monofunctional methanesulphonic acid esters: possible role of alkylation mechanisms.	2006 Dec 1	17011536
Autoxidative activation of the nematocide 1,3-dichloropropene to highly genotoxic and mutagenic derivatives: consideration of genotoxic/carcinogenic mechanisms.	2006 Jul	16841964
New potent and selective cytochrome P450 2B6 (CYP2B6) inhibitors based on three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis.	2007 Apr	17325652
Genotoxicity profiles of common alkyl halides and esters with alkylating activity.	2007 Oct 4	17644026
Synthesis, spectroscopy and alkylating properties of Pd(II) complexes of phosphorohydrazones of coumarin and chromone with potential antibacterial activity.	2007 Sep-Oct	18540163
Abstracts of papers presented at the 2008 pittsburgh conference.	2008	19365566
Chemical reactivity and biological activity of diketene.	2008 Oct	18759502
Sorbate-nitrite interactions: acetonitrile oxide as an alkylating agent.	2009 Jul	19580248
Decreased susceptibility of the cytochrome P450 2B6 variant K262R to inhibition by several clinically important drugs.	2009 Mar	19074527
4-(4-Nitro-benz-yl)pyridinium 5-nitro-salicylate.	2010 Apr 24	21579214
Alkylating potential of oxetanes.	2010 Jul 19	20550097
4-Amino-benzoic acid-1,2-bis-(4-pyrid-yl)ethane (2/1).	2010 Jun 5	21587796
4-Amino-benzoic acid-4,4'-(propane-1,3-diyl)dipyridine (1/1).	2010 Oct 9	21588953

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:53:08 GMT 2023` Edited by `admin` on `Fri Dec 15 18:53:08 GMT 2023`
Record UNII	0Z6GS37N7H
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

4-(4-NITROBENZYL)PYRIDINE

Systematic Name

English

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

Systematic Name

English

4-(P-NITROBENZYL)PYRIDINE

Common Name

English

NSC-83591

Code

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