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454257

2-Bromo-5-nitroaniline

97%

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About This Item

Linear Formula:
BrC6H3(NO2)NH2
CAS Number:
10403-47-1
Molecular Weight:
217.02
NACRES:
NA.22
PubChem Substance ID:
24868904
UNSPSC Code:
12352100
EC Number:
233-874-9
MDL number:
MFCD00051578
Assay:
97%
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assay

97%

mp

139-141 °C (lit.)

SMILES string

Nc1cc(ccc1Br)[N+]([O-])=O

InChI

1S/C6H5BrN2O2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H,8H2

InChI key

BAAUCXCLMDAZEL-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ4872
MKBR2050V
MKBN7930V
MKBF6903V
MKBC3423

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An intramolecular palladium-catalysed aryl amination reaction to produce benzimidazoles.
Brain CT and Brunton SA.
Tetrahedron Letters, 43(10), 1893-1895 (2002)
Olivier Baudoin et al.
Bioorganic & medicinal chemistry, 10(11), 3395-3400 (2002-09-06)
An improvement of the synthesis of biphenyl-carbamate 2a, the most active analogue of rhazinilam 1 so far, was performed using the Pd-catalyzed borylation/Suzuki coupling (BSC) method developed in our laboratories. The preparation of A-ring analogues of 2a bearing electron-withdrawing or
Formation and rearrangement of ipso intermediates in aromatic free-radical chlorination reactions.
Everly CR and Traynham JG.
The Journal of Organic Chemistry, 44(11), 1784-1787 (1979)
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Global Trade Item Number

SKUGTIN
454257-5G04061832100142