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Merck

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:
Peso molecular:
217.02
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22

grado

technical grade

Nivel de calidad

Análisis

90%

formulario

solid

mp

159-162 °C (lit.)

grupo funcional

bromo
carboxylic acid

cadena SMILES

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)

Clave InChI

IEJOONSLOGAXNO-UHFFFAOYSA-N

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Descripción general

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.

Aplicación

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

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves


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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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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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