516929
2-Amino-3-bromo-5-nitrobenzonitrile
97%
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About This Item
Linear Formula:
H2NC6H2(Br)(NO2)CN
CAS Number:
Molecular Weight:
242.03
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
241-574-4
MDL number:
Assay:
97%
InChI key
MUHLVSZIVTURCZ-UHFFFAOYSA-N
InChI
1S/C7H4BrN3O2/c8-6-2-5(11(12)13)1-4(3-9)7(6)10/h1-2H,10H2
SMILES string
Nc1c(Br)cc(cc1C#N)[N+]([O-])=O
assay
97%
mp
180-185 °C (lit.)
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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The conversion of 2-(4-chloro-5H-1, 2, 3-dithiazolylideneamino) benzonitriles into 3-aminoindole-2-carbonitriles using triphenylphosphine.
Michaelidou SS and Koutentis PA.
Tetrahedron, 65(40), 8428-8433 (2009)
P David Josephy et al.
Environmental and molecular mutagenesis, 57(1), 10-16 (2015-09-24)
Genotoxicity data on commercial azo dyes and their components remain sparse, despite their widespread use. We have tested the mutagenicity of 2-cyano-4-nitroaniline (CNNA) and 2,6-dicyano-4-nitroaniline (CNCNNA), components of azo dyes such as Disperse Blue 165 and Disperse Red 73, in
Vilas Venunath Patil et al.
The Journal of organic chemistry, 80(16), 7876-7883 (2015-07-28)
Unusual regio- and chemoselective oxidation of aromatic amines hindered with ortho substituents (except -NH2, -NHCH3, and -OH) to the corresponding nitro compounds is described by use of nonanebis(peroxoic acid). The mechanistic investigation for selective oxidation of amines ortho-substituted with -NH2
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