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Documentos

367931

Sigma-Aldrich

2-Bromo-4-fluorobenzoic acid

97%

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About This Item

Fórmula lineal:
BrC6H3(F)CO2H
Número de CAS:
1006-41-3
Peso molecular:
219.01
MDL number:
MFCD00055370
UNSPSC Code:
12352100
PubChem Substance ID:
24862867
NACRES:
NA.22

assay

97%

form

solid

mp

172-176 °C (lit.)

SMILES string

OC(=O)c1ccc(F)cc1Br

InChI

1S/C7H4BrFO2/c8-6-3-4(9)1-2-5(6)7(10)11/h1-3H,(H,10,11)

InChI key

RRKPMLZRLKTDQV-UHFFFAOYSA-N

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General description

Amination of 2-bromo-4-fluorobenzoic acid with aniline is reported to yield N-phenyl-4-fluoro-anthranilic acid.

Application

2-Bromo-4-fluorobenzoic acid may be used in the synthesis of:
  • 3-fluoro-8-(methylthio)dibenzo[b,f]thiepin-10(11H)-one
  • 2-fluoro-8-(methylthio)dibenzo[b,f]thiepin-10(11H)-one
  • 2-((2-carboxy-5-fluorophenyl)amino)-3-methoxybenzoic acid
  • 2-bromo-4-fluorobenzamide

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

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Kopicova Z, et al.
Collection of Czechoslovak Chemical Communications, 40(11), 3519-3529 (1975)
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Bioorganic & medicinal chemistry, 19(7), 2190-2198 (2011-03-23)
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Organic & biomolecular chemistry, 9(7), 2233-2239 (2011-02-08)
A Heck cyclisation approach is described for the rapid synthesis of a library of natural product-like small molecules, based on the phenanthridine core. The synthesis of a range of substituted benzylamine building blocks and their incorporation into the library is
Christian Wolf et al.
The Journal of organic chemistry, 71(8), 3270-3273 (2006-04-08)
A chemo- and regioselective copper-catalyzed cross-coupling procedure for amination of 2-bromobenzoic acids is described. The method eliminates the need for acid protection and produces N-aryl and N-alkyl anthranilic acid derivatives in up to 99% yield. N-(1-Pyrene)anthranilic acid has been employed
Fu-Xiang Wang et al.
Developmental cell, 54(6), 742-757 (2020-08-07)
Plant somatic embryogenesis refers to a phenomenon where embryos develop from somatic cells in the absence of fertilization. Previous studies have revealed that the phytohormone auxin plays a crucial role in somatic embryogenesis by inducing a cell totipotent state, although

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