560170
2-Bromo-4-methylbenzoic acid
97%
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About This Item
Linear Formula:
Br(CH3)C6H3COOH
CAS Number:
Molecular Weight:
215.04
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
2-Bromo-4-methylbenzoic acid, 97%
InChI
1S/C8H7BrO2/c1-5-2-3-6(8(10)11)7(9)4-5/h2-4H,1H3,(H,10,11)
SMILES string
Cc1ccc(C(O)=O)c(Br)c1
InChI key
ZZYYOHPHSYCHQG-UHFFFAOYSA-N
assay
97%
form
solid
mp
143-147 °C (lit.)
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
General description
2-Bromo-4-methylbenzoic acid can be prepared from 2-bromo-4-methylbenzonitrile via hydrolysis.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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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)
Intramolecular Reactions. IV. Chain Transfer Reaction Involving an Aromatic Hydrogen Atom and Related Reactions of 2-(4'-Methylbenzoyl)-benzenediazonium Salts1.
DeTar DF and Relyea DI.
Journal of the American Chemical Society, 78(17), 4302-4305 (1955)
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