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Methyl 3-bromo-4-methylbenzoate

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CAS:104901-43-1
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Methyl 3-bromo-4-methylbenzoate manufacturers

Methyl 3-bromo-4-methylbenzoate Basic information
Product Name:Methyl 3-bromo-4-methylbenzoate
Synonyms:METHYL 4-BROMO-M-TOLUATE;Benzoicacid, 3-bromo-4-methyl-, methyl ester;METHYL 3-BROMO-4-METHYLBENZOATE;METHYL 3-BROMO-P-TOLUATE;3-BROMO-4-METHYL METHYL BENZOATE;3-BROMO-4-METHYLBENZOIC ACID METHYL ESTER;4-BROMO-3-METHYLBENZOIC ACID METHYL ESTER;4-BROMO-M-TOLUIC ACID METHYL ESTER
CAS:104901-43-1
MF:C9H9BrO2
MW:229.07
EINECS:
Product Categories:Acids & Esters;Bromine Compounds;Aromatic Esters
Mol File:104901-43-1.mol
Methyl 3-bromo-4-methylbenzoate Structure
Methyl 3-bromo-4-methylbenzoate Chemical Properties
Melting point 38-44 °C(lit.)
Boiling point 130°C/0.1mmHg(lit.)
density 1.433±0.06 g/cm3(Predicted)
refractive index 1.5570 to 1.5610
Fp >230 °F
storage temp. Inert atmosphere,Room Temperature
solubility Soluble in dimethyl sulfoxide.
form clear liquid
color Colorless to Light orange to Yellow
InChIInChI=1S/C9H9BrO2/c1-6-3-4-7(5-8(6)10)9(11)12-2/h3-5H,1-2H3
InChIKeyMASRAGFWFYHMFI-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=C(C)C(Br)=C1
CAS DataBase Reference104901-43-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 2916399090
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
Methyl 3-bromo-4-methylbenzoate Usage And Synthesis
Chemical PropertiesOrange-red solid
UsesIt is a pharmaceutical intermediate.
Synthesis Reference(s)The Journal of Organic Chemistry, 53, p. 5545, 1988 DOI: 10.1021/jo00258a030
Synthesis
Methanol

67-56-1

3-Bromo-4-methylbenzoic acid

7697-26-9

Methyl 3-bromo-4-methylbenzoate

104901-43-1

The general procedure for the synthesis of methyl 3-bromo-4-methylbenzoate from methanol and 3-bromo-4-methylbenzoic acid was as follows: 3-bromo-4-methylbenzoic acid (2.0 g, 9.30 mmol) was suspended in methanol (20 ml), and sulfuric acid (0.04 ml) was added as a catalyst. The reaction mixture was stirred at 60°C for 42 hours. After completion of the reaction, the reaction mixture was concentrated and the residue was dissolved in ethyl acetate. The organic phase was washed with saturated aqueous sodium bicarbonate, dried over anhydrous magnesium sulfate, filtered and concentrated to afford the title compound methyl 3-bromo-4-methylbenzoate as an orange oil (2.25 g, quantitative yield), which could be used for subsequent experiments without further purification.

References[1] Patent: US2013/237537, 2013, A1. Location in patent: Paragraph 0330-0331
[2] Patent: WO2013/119946, 2013, A1. Location in patent: Paragraph 0198; 0345
[3] Patent: WO2011/107608, 2011, A1. Location in patent: Page/Page column 69
[4] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 23, p. 6442 - 6446
[5] Patent: WO2006/4903, 2006, A2. Location in patent: Page/Page column 125
Tag:Methyl 3-bromo-4-methylbenzoate(104901-43-1) Related Product Information
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