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Merck
CN

560170

2-溴-4-甲基苯甲酸

97%

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关于此项目

线性分子式:
Br(CH3)C6H3COOH
化学文摘社编号:
分子量:
215.04
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
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assay

97%

form

solid

mp

143-147 °C (lit.)

SMILES string

Cc1ccc(C(O)=O)c(Br)c1

InChI

1S/C8H7BrO2/c1-5-2-3-6(8(10)11)7(9)4-5/h2-4H,1H3,(H,10,11)

InChI key

ZZYYOHPHSYCHQG-UHFFFAOYSA-N

General description

2-Bromo-4-methylbenzoic acid can be prepared from 2-bromo-4-methylbenzonitrile via hydrolysis.

Application

2-Bromo-4-methylbenzoic acid may be used to synthesize:
  • 4′-hydroxy-5:6′-dimethyldibenzo-α-pyrone
  • 2-bromo-4-methylbenzophenone
  • 7-hydroxy-5′-methyl-6-n-hexyl-3:4-benzocoumarin
  • 2-(trimethylsilyl)ethyl 2-bromo-4-methylbenzoate


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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Studies in the biochemistry of micro-organisms. 90. Alternariol and alternariol monomethyl ether, metabolic products of Alternaria tenuis.
Raistrick H, et al.
The Biochemical Journal, 55(3), 421-421 (1953)
204. Tetrahydrodibenzopyran derivatives isomeric with tetrahydrocannabinols.
Avison AWD, et al.
Journal of the Chemical Society, 952-955 (1949)
A Radioiodinated MIBG-octreotate conjugate exhibiting enhanced uptake and retention in sstr2-expressing tumor cells.
Vaidyanathan G, et al.
Bioconjugate Chemistry, 18(6), 2122-2130 (2007)



全球贸易项目编号

货号GTIN
560170-5G04061831821529
560170-1G04061832583365