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153494

Sigma-Aldrich

2-Amino-5-nitrobenzonitrile

95%

Synonym(s):

2-Cyano-4-nitroaniline, 5-Nitroanthranilonitrile

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About This Item

Linear Formula:
O2NC6H3(NH2)CN
CAS Number:
17420-30-3
Molecular Weight:
163.13
Beilstein:
1425714
EC Number:
241-446-8
MDL number:
MFCD00007362
UNSPSC Code:
12352100
PubChem Substance ID:
24849349
NACRES:
NA.22

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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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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Deleterious substance

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

153494-5G:4548173107011
153494-100G:4548173106991
153494-BULK:
153494-VAR:
153494-500G:4548173107004

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Certificates of Analysis (COA)

Lot/Batch Number
STBH1641
STBH0648
STBF3081V
STBF4071V
S46185

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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
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
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
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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