4-(2-Methoxyphenyl)benzaldehyde

4-(2-Methoxyphenyl)benzaldehyde Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
Email: sales@chemwish.com
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Tel: 021-50135380
Email: shchemsky@sina.com
Company Name: Amatek Scientific Co. Ltd.  
Tel: 0512-56316828 4008675858
Email: sales@amateksci.com
Company Name: ShangHai Yuchuan Pharmaceutical Technology Co., Ltd.  
Tel: 02161555100
Email:
4-(2-Methoxyphenyl)benzaldehyde Basic information
Product Name:4-(2-Methoxyphenyl)benzaldehyde
Synonyms:AKOS BAR-0190;2'-METHOXY[1,1'-BIPHENYL]-4-CARBALDEHYDE;2'-METHOXY[1,1'-BIPHENYL]-4-CARBOXALDEHYDE;2'-METHOXY-BIPHENYL-4-CARBALDEHYDE;2'-METHOXY-BIPHENYL-4-CARBOXALDEHYDE;TIMTEC-BB SBB010158;4-(2-Methoxyphenyl)benzaldehyde, 2-(4-Formylphenyl)anisole, 4-Formyl-2-methoxybiphenyl;2'-methoxy-[1,1'-biphenyl]-4-carbaldehyde
CAS:421553-62-0
MF:C14H12O2
MW:212.24
EINECS:
Product Categories:pharmacetical
Mol File:421553-62-0.mol
4-(2-Methoxyphenyl)benzaldehyde Structure
4-(2-Methoxyphenyl)benzaldehyde Chemical Properties
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
CAS DataBase Reference421553-62-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
HazardClass IRRITANT
HS Code 2913000090
MSDS Information
4-(2-Methoxyphenyl)benzaldehyde Usage And Synthesis
Uses2''-Methoxy-biphenyl-4-carbaldehyde
Synthesis
2-Methoxyphenylboronic acid

5720-06-9

4-Bromobenzaldehyde

1122-91-4

4-(2-METHOXYPHENYL)BENZALDEHYDE

421553-62-0

The general procedure for the synthesis of 2'-methoxybiphenyl-4-carbaldehyde from 2-methoxyphenylboronic acid and p-bromobenzaldehyde is as follows: to a round-bottomed flask fitted with a stirring magnet are added 2-methoxyphenylboronic acid (275 mmol), p-bromobenzaldehyde (250 mmol), a base (375 mmol), a catalyst of 1.0 mol/L (9.2 mg), and a solvent (4 mL) . The flask inlet was sealed with a rubber septum and the internal air was displaced by nitrogen. The reaction mixture was stirred at room temperature for a certain time and then diluted with deionized water (5 mL) and ether (5 mL). The organic layer was separated and concentrated under reduced pressure.

References[1] Journal of Chemical Research, 2004, # 9, p. 593 - 595
[2] Advanced Synthesis and Catalysis, 2004, vol. 346, # 13-15, p. 1669 - 1673
[3] Synthesis, 2005, # 4, p. 537 - 542
[4] Tetrahedron Letters, 2018, vol. 59, # 31, p. 2989 - 2993
[5] ChemCatChem, 2016, vol. 8, # 4, p. 743 - 750
4-(2-Methoxyphenyl)benzaldehyde Preparation Products And Raw materials
Raw materials2-Methoxyphenylboronic acid-->4-Bromobenzaldehyde-->Sodium carbonate-->Methanol
Tag:4-(2-Methoxyphenyl)benzaldehyde(421553-62-0) Related Product Information
4-(4-METHOXYPHENYL)BENZALDEHYDE 4-(3-Methoxyphenyl)benzaldehyde 4-(2-Methoxyphenyl)benzaldehyde 2-Methoxybiphenyl 4-(2-Fluoro-3-methoxyphenyl)benzaldehyde 4-(5-Chloro-2-methoxyphenyl)benzaldehyde,4-(4-Chloro-2-methoxyphenyl)benzaldehyde,4-(4-Chloro-3-methoxyphenyl)benzaldehyde 4-(3-Chloro-4-methoxyphenyl)benzaldehyde,4-(3-Chloro-5-methoxyphenyl)benzaldehyde 4-(2-Cyano-4-(trifluoromethyl)phenyl)benzaldehyde 3-(2-Fluoro-3-methoxyphenyl)benzaldehyde 4-(2,3-Dimethoxyphenyl)benzoic acid 2'-Methoxy-biphenyl-4-carboxylic acid 2'-Methoxy-biphenyl-3-carbaldehyde 3-(4-Methoxyphenyl)benzaldehyde 3-(3-Methoxyphenyl)benzaldehyde Benzoxanthene yellow allocolchicine 3-methoxy-2-phenyl-1H-naphtho[2,1,8-mna]xanthen-1-one 4'-(2-METHOXYPHENYL)-2,2,2-TRIFLUOROACETOPHENONE