methyl 4-(bromomethyl)-2-methoxybenzoate

methyl 4-(bromomethyl)-2-methoxybenzoate Suppliers list
Company Name: Anhui Yongsheng Pharmaceutical Technology Co., Ltd  Gold
Tel: 3307 18017383231
Email: 983544897@qq.com
Company Name: JinYan Chemicals(ShangHai) Co.,Ltd.  
Tel: 13817811078
Email: sales@jingyan-chemical.com
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
Email: info@hanhongsci.com
Company Name: Baiyin Chengze Chemical Technology Co., Ltd.  
Tel: +86 943-8535351 13389336721
Email: sales@chengzechem.com
Company Name: Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.  
Tel: 025-66113011 13913916777
Email: cfzhang@aikonchem.com

methyl 4-(bromomethyl)-2-methoxybenzoate manufacturers

methyl 4-(bromomethyl)-2-methoxybenzoate Basic information
Product Name:methyl 4-(bromomethyl)-2-methoxybenzoate
Synonyms:methyl 4-(bromomethyl)-2-methoxybenzoate;2-Methoxy-4-(broMoMethyl)benzoic acid Methyl ester;4-broMoMethyl-2-Methoxy benzoic acid Methyl ester;Methyl 2-Methoxy-4-(bromomethyl)benzoate;Benzoic acid, 4-(bromomethyl)-2-methoxy-, methyl ester;)-2-methoxybenzoate;Oxirane, 2-[7-(phenylMethoxy)ethyl]-
CAS:74733-27-0
MF:C10H11BrO3
MW:259.1
EINECS:
Product Categories:
Mol File:74733-27-0.mol
methyl 4-(bromomethyl)-2-methoxybenzoate Structure
methyl 4-(bromomethyl)-2-methoxybenzoate Chemical Properties
Boiling point 142-146 °C(Press: 1.8 Torr)
density 1.432±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
AppearanceWhite to off-white Solid
InChIInChI=1S/C10H11BrO3/c1-13-9-5-7(6-11)3-4-8(9)10(12)14-2/h3-5H,6H2,1-2H3
InChIKeyDCXFLSHDURQRML-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=C(CBr)C=C1OC
Safety Information
MSDS Information
methyl 4-(bromomethyl)-2-methoxybenzoate Usage And Synthesis
Synthesis
METHYL 2-METHOXY-4-METHYLBENZOATE

81245-24-1

methyl 4-(bromomethyl)-2-methoxybenzoate

74733-27-0

General procedure for the synthesis of methyl 4-bromomethyl-2-methoxybenzoate from methyl 2-methoxy-4-methylbenzoate: over a period of 1.5 h, bromine (6.19 mL, 120 mmol) was slowly added dropwise over a period of 1.5 h to a reflux mixture of methyl 2-methoxy-4-methylbenzoate (21.625 g, 120 mmol) in carbon tetrachloride (240 mL) dissolved in a carbon tetrachloride (75 mL). During the dropwise addition, the reaction mixture was irradiated using a 250W tungsten lamp. After dropwise addition, the reaction was continued at reflux for 15 minutes. Upon completion of the reaction, the mixture was concentrated and the solvent was removed under vacuum to afford methyl 4-bromomethyl-2-methoxybenzoate as an oily product (29.864 g, 96% yield). The product was confirmed by NMR hydrogen spectrum (400 MHz, CDCl3): δ 2.40 (s, 3H), 3.87 (s, 3H), 3.91 (s, 3H), 4.44 (s, 2H). Mass spectrometry (FIA-MS) showed the molecular ion peak m/e: 259 ([M+1]+).

References[1] Patent: WO2004/108677, 2004, A1. Location in patent: Page 199
[2] Synlett, 2014, vol. 25, # 17, p. 2485 - 2487
[3] Patent: US2009/209586, 2009, A1. Location in patent: Page/Page column 13
[4] Patent: KR2016/20674, 2016, A. Location in patent: Paragraph 0053; 0115; 0116
[5] Bulletin de la Societe Chimique de France, 1962, p. 2255 - 2261
Tag:methyl 4-(bromomethyl)-2-methoxybenzoate(74733-27-0) Related Product Information
METHYL 4-(BROMOMETHYL)-3-METHOXYBENZOATE 3-Cyanomethylbenzoic acid methyl ester 2-Bromo-5-methoxytoluene Bis(2-ethylhexyl) phthalate METHYL 2-METHOXY-4-METHYLBENZOATE methyl 4-formyl-2-methoxybenzoate