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153494

Sigma-Aldrich

2-Amino-5-nitrobenzonitrile

95%

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Synonym(s):
2-Cyano-4-nitroaniline, 5-Nitroanthranilonitrile
Linear Formula:
O2NC6H3(NH2)CN
CAS Number:
17420-30-3
Molecular Weight:
163.13
Beilstein:
1425714
EC Number:
241-446-8
MDL number:
MFCD00007362
PubChem Substance ID:
24849349
NACRES:
NA.22

Quality Level

100

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

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1 of 4

This Item
A89901324698522457
2-Amino-5-nitrobenzonitrile 95%

Sigma-Aldrich

153494

2-Amino-5-nitrobenzonitrile

2-Aminobenzonitrile 98%

Sigma-Aldrich

A89901

2-Aminobenzonitrile

4-Amino-3-nitrobenzonitrile 98%

Sigma-Aldrich

324698

4-Amino-3-nitrobenzonitrile

3-Amino-5-nitrobenzisothiazole 97%

Sigma-Aldrich

522457

3-Amino-5-nitrobenzisothiazole

form

powder

form

crystals

form

-

form

-

mp

200-207 °C (lit.)

mp

45-48 °C (lit.)

mp

159-162 °C (lit.)

mp

250 °C (dec.) (lit.)

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
Anton Georgiev et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 175, 76-91 (2016-12-27)
In this paper three different "push-pull" 4-aminoazobenzene dyes have been synthesized in order to characterize their photochromic behavior in different solvents. The molecular geometry was optimized by DFT/B3LYP functional combined with the standard 6-31+G(d,p) basis set for trans (E) and
Jie Hu et al.
Chemical biology & drug design, 85(6), 672-684 (2014-10-21)
Quinazoline has been reported to exhibit multiple bioactivities. The aim of this study was to discover new quinazoline derivatives with preventive effect on lipopolysaccharide-induced acute lung injury via anti-inflammatory actions. Thirty-three 4-amino quinazolin derivatives were synthesized and screened for anti-inflammatory

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