Basic information Safety Supplier Related

2-methoxy-4-methyl-benzaldehyde

Basic information Safety Supplier Related

2-methoxy-4-methyl-benzaldehyde Basic information

Product Name:
2-methoxy-4-methyl-benzaldehyde
Synonyms:
  • 2-methoxy-4-methyl-benzaldehyde
  • 4-Methyl-6-methoxybenzaldehyde
  • 2-methoxy-4-methylbenzaldehyde(SALTDATA: FREE)
  • Benzaldehyde, 2-methoxy-4-methyl-
CAS:
57415-35-7
MF:
C9H10O2
MW:
150.17
Mol File:
57415-35-7.mol
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2-methoxy-4-methyl-benzaldehyde Chemical Properties

Melting point:
40-43 ºC
Boiling point:
258 ºC
Density 
1.062
Flash point:
114 ºC
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
Light yellow to brown Solid
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Safety Information

HazardClass 
IRRITANT
HS Code 
2913000090
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2-methoxy-4-methyl-benzaldehyde Usage And Synthesis

Uses

2-Methoxy-4-methylbenzaldehyde acts as a reagent in the synthesis of [3,2-d]pyrimidine derivatives as week as in the synthesis of tachykinin NK2 receptor antagonists which may be used in the treatment of IBS.

Synthesis Reference(s)

Journal of Medicinal Chemistry, 35, p. 734, 1992 DOI: 10.1021/jm00082a014

Synthesis

698-27-1

74-88-4

57415-35-7

GENERAL METHODS: Potassium carbonate (K2CO3, 35 mg, 0.25 mmol) was added to a solution of anhydrous N,N-dimethylformamide (DMF, 6.0 mL) of 2-hydroxy-4-methylbenzaldehyde (34 mg, 0.25 mmol) and the mixture was stirred at room temperature for 30 min. Subsequently, iodomethane (CH3I, 30 μL, 68 mg, 0.5 mmol) was added and the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, distilled water was added to terminate the reaction and the aqueous phase was extracted three times with ethyl acetate (EtOAc). The organic phases were combined and dried over anhydrous magnesium sulfate (MgSO4) and subsequently concentrated under reduced pressure. The residue was purified by silica gel column chromatography.

References

[1] Beilstein Journal of Organic Chemistry, 2018, vol. 14, p. 734 - 746
[2] Synthesis (Germany), 2017, vol. 49, # 1,

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