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Sigma-Aldrich

2-Bromo-5-fluoroaniline

97%

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About This Item

Linear Formula:
BrC6H3(F)NH2
CAS Number:
1003-99-2
Molecular Weight:
190.01
MDL number:
MFCD00070750
UNSPSC Code:
12352100
PubChem Substance ID:
24877625
NACRES:
NA.22

assay

97%

mp

43-47 °C (lit.)

SMILES string

Nc1cc(F)ccc1Br

InChI

1S/C6H5BrFN/c7-5-2-1-4(8)3-6(5)9/h1-3H,9H2

InChI key

FWTXFEKVHSFTDQ-UHFFFAOYSA-N

Application

2-Bromo-5-fluoroaniline may be used to synthesize:
  • orthobromothiobenzanilide of 5-fluoronitrobenzothiazole[1]
  • 2-bromo-5-fluorobenzo[14C]nitrile[2]
  • [3-14C]-5-fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole[2]
  • 2-bromo-5-fluoro-phenyl)-(2-methoxy-6-pentadecyl-benzyl)amine[3]

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_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBP8908V
MKAA2943V
MKAA2943
09610DJ
U21116

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T D Bradshaw et al.
Current medicinal chemistry, 11(8), 1009-1021 (2004-04-14)
This review traces the development of a series of potent and selective antitumour benzothiazoles from the discovery of the initial lead compound, 2-(4-amino-3-methylphenyl)benzothiazole (DF 203) in 1995 to the identification of a clinical candidate, Phortress, scheduled to enter Phase 1
Synthesis of isotopically labelled [3-14C]-and [3, 3-2H2]-5-fluoro-1, 3-dihydro-1-hydroxy-2, 1-benzoxaborole (AN2690), a new antifungal agent for the potential treatment of onychomycosis.
Baker SJ, et al.
Journal of Labelled Compounds & Radiopharmaceuticals, 50(4), 245-250 (2007)
Synthesis of novel benzylamine analogues of Anacardic acid as potent antibacterial agents.
Dubey PK.
Der Pharma Chemica, 3(6), 500-512 (2011)

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