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Key Documents

N14204

Sigma-Aldrich

4-(4-Nitrobenzyl)pyridine

98%

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About This Item

Empirical Formula (Hill Notation):
C12H10N2O2
CAS Number:
Molecular Weight:
214.22
Beilstein/REAXYS Number:
170877
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

crystals

mp

69-71 °C (lit.)

SMILES string

[O-][N+](=O)c1ccc(Cc2ccncc2)cc1

InChI

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

InChI key

MNHKUCBXXMFQDM-UHFFFAOYSA-N

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Application

Used in tests for alkylating agents[1] and in a spectroscopic method for phosgene determination.[2]

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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P G Penketh et al.
Journal of medicinal chemistry, 37(18), 2912-2917 (1994-09-02)
1,2-Bis(sulfonyl)-1-alkylhydrazines are highly active experimental antineoplastic agents which decompose with first-order kinetics in neutral aqueous solutions. These agents generate approximately 2 mol of the corresponding sulfinate, 1 mol of nitrogen, and 1 mol of the appropriate alcohol, produced as a
J A Freeman et al.
Analytical chemistry, 66(11), 1902-1910 (1994-06-01)
A promising instrumental technique has been investigated to rapidly screen complex environmental samples for chemical contaminants having the propensity to covalently bond to biomacromolecules such as DNA. Radical molecular ions of pyridine, a model compound for nucleophilic bases of DNA
Timothy J Schrader et al.
Teratogenesis, carcinogenesis, and mutagenesis, 22(6), 425-441 (2002-10-24)
Bisphenol A (4,4'-isopropylidenediphenol) is a common component of polycarbonate plastics and epoxy resins. Since bisphenol A-containing plastics and resins have found uses in food-contact items, its potential migration into foodstuffs and possible health consequences have been the focus of many
Shino Manabe et al.
Journal of the American Chemical Society, 124(43), 12638-12639 (2002-10-24)
On-resin real-time monitoring by a combination of a color test of (p-nitrobenzyl)pyridine and Disperse Red was developed for oligosaccharide synthesis.
H B Jiang et al.
Biochemical pharmacology, 60(4), 571-579 (2000-06-30)
Mitomycin C (MC) requires bioreduction prior to the generation of alkylating moieties. NADPH-cytochrome P450 reductase is predominant in metabolic activation of MC in hypoxic cancer cells. In this study, neuronal nitric oxide synthase (nNOS), whose reductase domain is structurally similar

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