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Merck
CN

190268

2,6-二溴-4-硝基苯胺

≥97%

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关于此项目

线性分子式:
Br2C6H2(NO2)NH2
化学文摘社编号:
827-94-1
分子量:
295.92
NACRES:
NA.22
PubChem Substance ID:
24851424
UNSPSC Code:
12352100
EC Number:
212-577-8
MDL number:
MFCD00007639
Assay:
≥97%

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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

100

functional group

bromo, nitro

相关类别

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
STBK5426
STBK2854
STBK2178
STBH3337
STBF5493V

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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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