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461814

Sigma-Aldrich

5-Bromosalicylic acid

technical grade, 90%

Sinónimos:

5-Bromo-2-hydroxybenzoic acid

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About This Item

Fórmula lineal:
BrC6H3-2-(OH)CO2H
Número de CAS:
89-55-4
Peso molecular:
217.02
EC Number:
201-917-0
MDL number:
MFCD00002455
UNSPSC Code:
12352100
PubChem Substance ID:
24869910
NACRES:
NA.22

grade

technical grade

Quality Level

100

assay

90%

form

solid

mp

159-162 °C (lit.)

SMILES string

OC(=O)c1cc(Br)ccc1O

InChI

1S/C7H5BrO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,(H,10,11)

InChI key

IEJOONSLOGAXNO-UHFFFAOYSA-N

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Categorías relacionadas

General description

5-Bromosalicylic acid is a salicylic acid derivative. Its bonding to viscose fabric can impart antibacterial properties to the fabric. It has been identified as one of the brominated disinfection byproduct (Br-DBP) formed during the chlorination of saline sewage effluents.

Application

5-Bromosalicylic acid may be employed as a starting reagent for the synthesis of honokiol, a biphenyl-type neolignan.

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

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A Kantouch et al.
International journal of biological macromolecules, 62, 603-607 (2013-10-01)
Salicylic acid and three of its derivatives were used to provide antibacterial properties to viscose fabrics. The four bactericides used were bonded to the viscose fabrics using epichlorohydrin or polymer binders. Optimization of the salicylic acid and its derivatives as
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Bioorganic & medicinal chemistry letters, 14(10), 2621-2625 (2004-04-28)
Honokiol, a biphenyl-type neolignan, which shows the remarkable neurotrophic effect in primary cultured rat cortical neurons, has been effectively synthesized in 21% yield over 14 steps starting from 5-bromosalicylic acid and p-hydroxybenzoic acid by utilizing Pd-catalyzed Suzuki-Miyaura coupling reaction as
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