ChemicalBook--->CAS DataBase List--->421553-62-0

421553-62-0

421553-62-0 Structure

421553-62-0 Structure
IdentificationMore
[Name]

4-(2-METHOXYPHENYL)BENZALDEHYDE
[CAS]

421553-62-0
[Synonyms]

2'-METHOXY[1,1'-BIPHENYL]-4-CARBALDEHYDE
2'-METHOXY[1,1'-BIPHENYL]-4-CARBOXALDEHYDE
2'-METHOXY-BIPHENYL-4-CARBALDEHYDE
2'-METHOXY-BIPHENYL-4-CARBOXALDEHYDE
4-(2-METHOXYPHENYL)BENZALDEHYDE
AKOS BAR-0190
TIMTEC-BB SBB010158
[Molecular Formula]

C14H12O2
[MDL Number]

MFCD01631913
[Molecular Weight]

212.24
[MOL File]

421553-62-0.mol
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[CAS DataBase Reference]

421553-62-0(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2913000090
Hazard InformationBack Directory
[Uses]

2''-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
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