N14204
4-(4-硝基苄基)吡啶
98%
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关于此项目
经验公式（希尔记法）:
C12H10N2O2
化学文摘社编号:
分子量:
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
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
SMILES string
[O-][N+](=O)c1ccc(Cc2ccncc2)cc1
assay
98%
form
crystals
mp
69-71 °C (lit.)
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Application
用于烷基化试剂的测试 以及用于光谱法测定光气。
存储类别
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
Marcio Fronza et al.
Phytochemistry, 78, 107-119 (2012-03-23)
Abietane diterpenes, especially those containing quinone moieties, are often reported to have cytotoxic effects on cancer cell lines. They deserve greater attention because several cancer chemotherapeutic agents also possess the quinone structural feature. To date, very little is known about
S K Dangwal
Industrial health, 32(1), 41-47 (1994-01-01)
A reagent consisting of 0.4% of nitrobenzyl pyridine and 0.5% of sodium acetate in ethanol was found to be applicable as a sampling and coloring solution to a sensitive and relatively specific spectrophotometric determination of phosgene. This method is a
Use of 4-(nitrobenzyl)pyridine (4-NBP) to test mutagenic potential of slow-reacting epoxides, their corresponding olefins, and other alkylating agents.
J H Kim et al.
Bulletin of environmental contamination and toxicology, 49(6), 879-885 (1992-12-01)
Rafael Gómez-Bombarelli et al.
Chemical research in toxicology, 25(6), 1176-1191 (2012-04-07)
Alkylating agents are considered to be archetypal carcinogens. One suitable technique to evaluate the activity of alkylating compounds is the NBP assay. This method is based on the formation of a chromophore in the reaction between the alkylating agent and
Marina González-Pérez et al.
Chemical research in toxicology, 25(12), 2755-2762 (2012-11-23)
The chemical reactivity of the mutagenic epoxides (EP) propylene oxide (PO), 1,2-epoxybutane (1,2-EB), and cis- and trans-2,3-epoxybutane (cis- and trans-2,3-EB) with 4-(p-nitrobenzyl)pyridine (NBP), a bionucleophile model for S(N)2 alkylating agents with high affinity for the guanine-N7 position, was investigated kinetically.
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