5-Bromo-2-methylbenzoic acid

5-Bromo-2-methylbenzoic acid Basic information
Product Name:5-Bromo-2-methylbenzoic acid
Synonyms:5-BROMO-2-METHYLBENZOIC ACID,98%;5-Bromo-2-methylbenzoic acid ,97%;2,3,4,6-tetrakis-O-triMethylsilyl-D-guluconolactone;5-Bromo-o-toluic acid, 4-Bromo-2-carboxytoluene;5 - broMine - 2 - Methyl benzoic acid;5-Bromo-2-methylbenzoic acid≥ 99% (HPLC);5-Bromo-2-methylbenzoic acid 97%;5-BROMO-2-METHYLBENZOIC ACID
CAS:79669-49-1
MF:C8H7BrO2
MW:215.04
EINECS:628-605-0
Product Categories:Aromatic Nitriles;C8;Carboxylic Acids;Phenyls & Phenyl-Het;Organic acids;Carbonyl Compounds;Acids & Esters;Bromine Compounds;Carboxylic Acids;Phenyls & Phenyl-Het;API;bc0001;79669-49-1
Mol File:79669-49-1.mol
5-Bromo-2-methylbenzoic acid Structure
5-Bromo-2-methylbenzoic acid Chemical Properties
Melting point 167-171°C
Boiling point 319.4±30.0 °C(Predicted)
density 1.599±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
solubility soluble in Methanol
pka3.48±0.25(Predicted)
form powder to crystal
color White to Almost white
InChIKeySEENCYZQHCUTSB-UHFFFAOYSA-N
CAS DataBase Reference79669-49-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-36/37/38
Safety Statements 26
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
HazardClass IRRITANT
PackingGroup 
HS Code 29163990
MSDS Information
5-Bromo-2-methylbenzoic acid Usage And Synthesis
Chemical PropertiesOff-white Powder.
Uses2-Methyl-5-bromobenzoic acid is used in organic synthesis and pharmaceutical intermediates. It is used in the synthesis of 5-bromo-2-methyl-N-(quinolin-8-yl)benzamide, (5-Bromo-2-methylphenyl)(thiophen-2-yl)-methanone and 2-(5-bromo-2-methylbenzyl)-5-(4-fluorophenyl)thiophene.
SynthesisIn a reaction vessel equipped with a mechanical stirrer, a solution of 2-methylbenzoic acid (10.00 g, 73.45 mmol, 1.0 equivalent) in concentrated sulfuric acid (15 mL) at room temperature, bromine (17.6 g, 110.14 mmol, 1. 5 equivalents) was added dropwise over 10 minutes and stirred at 25 ° C. for 20 hours. The reaction solution was injected into ice water (60 ml), and the precipitated solid was filtered, washed with water (20 mL), and air-dried at 60 ° C. overnight to obtain a bromo compound (15.2 g, 97%, addition rate: 95.7).5-Br body / 3-Br body = 62: 38). The obtained crude bromo compound (3 g) was dissolved in ethanol (9 mL) at 70 ° C., cooled to 20 ° C., and stirred at the same temperature for 30 minutes at 10 ° C. or lower for 3 hours. The precipitated crystals were filtered and air-dried at 60 ° C. overnight to obtain 5-Bromo-2-methylbenzoic acid(1.19 g, 5-Br / 3-Br = 91: 9, total yield: 38.5%).
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methylbenzoic acid Methylparaben 4-BROMO-2-METHYLBENZOIC ACID,4-Bromo-2-methylbenzoic acid, 98+%,4-Bromo-2-Methylbenzoic Acid 2-Methyl-4-Bromobenzoic Acid Methyl 2-bromobenzoate Methyl 3-(Trifluoromethyl)benzoic acid 4-Bromobenzoic acid Ethyl 2-(Chlorosulfonyl)acetate m-Toluic acid 3-Bromoanisole 3-BROMO-2-METHYLBENZOIC ACID 98%,3-BROMO-2-METHYLBENZOIC ACID Folic acid o-Toluic acid Kresoxim-methyl Methyl 4-(bromomethyl)benzoate Bromine phosphoric acid Methyl bromide

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