190268
2,6-Dibromo-4-nitroaniline
≥97%
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About This Item
Linear Formula:
Br2C6H2(NO2)NH2
CAS Number:
Molecular Weight:
295.92
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-577-8
MDL number:
Assay:
≥97%
mp
205-207 °C (lit.)
functional group
bromo, nitro
InChI key
YMZIFDLWYUSZCC-UHFFFAOYSA-N
InChI
1S/C6H4Br2N2O2/c7-4-1-3(10(11)12)2-5(8)6(4)9/h1-2H,9H2
SMILES string
Nc1c(Br)cc(cc1Br)[N+]([O-])=O
assay
≥97%
Quality Level
Related Categories
Application
2,6-Dibromo-4-nitroaniline has been used in the synthesis of:
- blue disperse dyes
- 7-bromo-5-iodo-4-oxo-1,4-dihydroquinoline-2-carboxylic acid
- diphenols-amides such as N-(2,6-dibromo-4-nitrophenyl)-4,4-bis(4-hydroxyphenyl)-pentanamide and N-(2,6-diiodo-4-nitrophenyl)-4,4-bis(4-hydroxyphenyl)-pentanamide
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
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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K Suresh Kumar et al.
Environmental monitoring and assessment, 127(1-3), 67-72 (2006-08-10)
Facile, selective and sensitive spectrophotometric method has been developed for the determination of bendiocarb in its insecticidal formulations, fortified water, food grains, agriculture wastewater and agriculture soil samples with prepared reagents. The method was based on alkaline hydrolysis of the
Polymerization by phase transfer catalysis. 24. Synthesis of condensation polymers derived from halogenated diphenol-amides with the amide group in the side chain.
Tagle LH, et al.
Polym. Bull., 42(6) (1999)
Substituent effects on the colour, dyeing and fastness properties of 4-phenylazo-1-naphthylamines and of 2-acetylamino-5-methoxy-4-N-?-cyanoethyl-N-?-hydroxyethylaminoazobenzene.
Peters AT.
Journal of the Society of Dyers and Colourists, 104(9), 344-348 (1988)
Synthesis of 7-Bromo-5-iodo-4-oxo-1, 4-dihydroquinoline-2-carboxylic acid.
Dumont F and Slegers G.
Bull. Soc. Chim. Belg., 104(8), 505-507 (1995)
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