4-Methoxy-2-methylbenzaldehyde

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Names

[ CAS No. ]:
52289-54-0

[ Name ]:
4-Methoxy-2-methylbenzaldehyde

[Synonym ]:
MFCD02261771
2-Methyl-p-anisaldehyde
VHR B1 DO1
4-Methoxy-2-methylbenzaldehyde
2-Methyl-4-methoxybenzaldehyde
Benzaldehyde, 4-methoxy-2-methyl-

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
264.1±20.0 °C at 760 mmHg

[ Molecular Formula ]:
C9H10O2

[ Molecular Weight ]:
150.174

[ Flash Point ]:
118.9±15.3 °C

[ Exact Mass ]:
150.068085

[ PSA ]:
26.30000

[ LogP ]:
2.16

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.542

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3.0

[ HS Code ]:
2912499000

Precursor & DownStream

Precursor

  • 4-Methoxy-1,2-dimethylbenzene
  • 4-Bromo-3-methyl-anisole
  • N,N-Dimethylformamide
  • 1-Methoxy-2,3-dimethylbenzene
  • zinc,dicyanide
  • 3-Methylanisole
  • 4-METHOXY-2-METHYLBENZYL ALCOHOL
  • 2-iodo-5-methoxystyrene oxide
  • 2-Iodo-5-methoxybenzaldehyde
  • (2-iodo-5-methoxyphenyl)methanol

DownStream

  • 2-Hydroxy-3-methylbenzaldehyde
  • methyl 4-methoxy-2-methylbenzoate
  • 4-Methoxy-1,2-dimethylbenzene
  • 4-METHOXY-2-METHYLBENZYLAMINE Hydrochloride
  • 4-Methoxy-2-methylbenzoic acid
  • 4-Hydroxy-2-methylbenzoic acid
  • ethyl 3-(4-methoxy-2-methylphenyl)prop-2-enoate
  • 4-(Benzyloxy)-2-methylbenzaldehyde
  • (4-Methoxy-2-methylphenyl)acetonitrile
  • 4-Methoxy-2-methylphenylacetic acid

Customs

[ HS Code ]: 2912499000

[ Summary ]:
2912499000. other aldehyde-ethers, aldehyde-phenols and aldehydes with other oxygen function. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

Antifungal activity of redox-active benzaldehydes that target cellular antioxidation.

Ann. Clin. Microbiol. Antimicrob. 10 , 23, (2011)

Disruption of cellular antioxidation systems should be an effective method for control of fungal pathogens. Such disruption can be achieved with redox-active compounds. Natural phenolic compounds can ...

Gas chromatography-mass spectrometry analysis of regioisomeric ring substituted methoxy methyl phenylacetones.

J. Chromatogr. Sci. 45(8) , 458-65, (2007)

The methoxy methyl phenylacetones share an isobaric relationship (equivalent mass but different elemental composition) to the controlled precursor substance 3,4-methylenedioxyphenylacetone. The 10 met...

Compounds of potential interest for the chemotherapy of leprosy. Buu-Hoï NP, et al.

J. Org. Chem. 21(4) , 415-418, (1956)


More Articles


Related Compounds

  • 5-ethoxy-4-methoxy-2-methylbenzaldehyde
  • 5-hydroxy-4-methoxy-2-methylbenzaldehyde
  • 5-(Benzyloxy)-4-Methoxy-2-Methylbenzaldehyde
  • 4-methoxy-2-(methoxymethoxy)-6-methylbenzaldehyde
  • 4-methoxy-5-methoxycarbonyloxy-2-methylbenzaldehyde
  • 4-methoxy-2-(3-trimethylsilylprop-2-ynyl)phenol