153494
2-氨基-5-硝基苯甲腈
95%
别名:
2-氰基-4-硝基苯胺, 5-硝基邻氨基苯甲腈
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关于此项目
线性分子式:
O2NC6H3(NH2)CN
化学文摘社编号:
分子量:
163.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-446-8
Beilstein/REAXYS Number:
1425714
MDL number:
Assay:
95%
Form:
powder
Quality Level
assay
95%
form
powder
mp
200-207 °C (lit.)
SMILES string
Nc1ccc(cc1C#N)[N+]([O-])=O
InChI
1S/C7H5N3O2/c8-4-5-3-6(10(11)12)1-2-7(5)9/h1-3H,9H2
InChI key
MGCGMYPNXAFGFA-UHFFFAOYSA-N
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Jinho Lee et al.
Bioorganic & medicinal chemistry letters, 18(7), 2292-2295 (2008-03-21)
A novel series of 3,5-diaminoindazoles were prepared and found to be CDK inhibitors. Potent inhibitors against CDK1 and CDK2 were obtained by introduction of 1lambda(6)-isothiazolidine-1,1-dioxide at 5-position of indazole. Anti-proliferative activities of compounds were evaluated using EJ, HCT116, SW620, and
Syed Muhammad Saad et al.
European journal of medicinal chemistry, 108, 13-20 (2015-12-01)
4-Arylamino-6-nitroquinazolines (2-25) were synthesized and evaluated for their leishmanicidal activities against Leishmania major promastigotes in vitro with IC50 values = 1.87-61.48 μM. Among the twenty four synthetic derivatives, 4-[4'-(methylsulfanyl)phenyl]amino-6-nitroquinazoline (21), and 4-(2'-methoxyphenyl)amino-6-nitroquinazoline (8) showed excellent antileishmanial activities with IC50 values 1.87 ± 0.31 and 4.37 ± 0.02 μM, respectively
Alexis Enright et al.
The Analyst, 129(10), 975-978 (2004-10-01)
A series of eleven specially designed benzotriazole monoazo dyes for use in surface enhanced resonance Raman scattering studies are reported. Unlike previous benzotriazole dyes produced for SERRS, these dyes have been synthesised to be trifunctional in nature. The presence of
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 153494-100G | 04061838740861 |