N14204
4-(4-Nitrobenzyl)pyridine
98%
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About This Item
Empirical Formula (Hill Notation):
C12H10N2O2
CAS Number:
Molecular Weight:
214.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-108-2
Beilstein/REAXYS Number:
170877
MDL number:
Assay:
98%
Form:
crystals
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
Application
Used in tests for alkylating agents and in a spectroscopic method for phosgene determination.
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Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Articles
DISCOVER Bioactive Small Molecules for Neuroscience
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| N14204-10G | 04061834109228 |
| N14204-100G | 04061834109181 |