2-(BENZYLOXY)-3-METHOXYBENZALDEHYDE

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Names

[ CAS No. ]:
2011-06-5

[ Name ]:
2-(BENZYLOXY)-3-METHOXYBENZALDEHYDE

[Synonym ]:
2-Benzyloxy-3-methoxy-benzaldehyd
2-Benzyloxy-3-methoxybenzaldehyde
MFCD00202674

Chemical & Physical Properties

[ Density]:
1.154g/cm3

[ Boiling Point ]:
386.9ºC at 760 mmHg

[ Melting Point ]:
44-46ºC(lit.)

[ Molecular Formula ]:
C15H14O3

[ Molecular Weight ]:
242.27000

[ Flash Point ]:
179.3ºC

[ Exact Mass ]:
242.09400

[ PSA ]:
35.53000

[ LogP ]:
3.08670

[ Vapour Pressure ]:
3.43E-06mmHg at 25°C

[ Index of Refraction ]:
1.59

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2912499000

Synthetic Route

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

Conjugation of benzylvanillin and benzimidazole structure improves DNA binding with enhanced antileukemic properties.

PLoS ONE 8(11) , e80983, (2013)

Benzyl-o-vanillin and benzimidazole nucleus serve as important pharmacophore in drug discovery. The benzyl vanillin (2-(benzyloxy)-3-methoxybenzaldehyde) compound shows anti-proliferative activity in ...

1D and 2D NMR Studies of Benzyl o-Vanillin. Al-Douh MH, et al.

Indo. J. Chem. 8(3) , 411-17, (2010)

2-Benzyloxy-3-methoxybenzaldehyde (benzyl-o-vanillin). Al-Douh MH, et al.

Acta Crystallogr. Sect. E Struct. Rep. Online 62(11) , 4768-70, (2006)


More Articles


Related Compounds

  • 2-(Benzyloxy)-5-chloro-3-methoxybenzaldehyde
  • (2-(Benzyloxy)-3,5-difluorophenyl)boronic acid
  • 2-benzyloxy-3-hydroxymethyl-1-methoxybenzene
  • 2-(benzyloxy)-3-(hexadecyloxy)propyl (2-bromoethyl) hydrogen phosphate
  • 2-(benzyloxy)-3,4-diphenylisoquinolin-1(2H)-one
  • 2-benzyloxy-3,5-dichloro-benzoic acid methyl ester
  • 3-Phenoxy-1-(2,2,2-trifluoroacetyl)azetidine-3-carboxylic acid
  • 1-(2,2,2-Trifluoroacetyl)-1,2,3,5-tetrahydro-4,1-benzoxazepine-8-carboxylic acid
  • 3-{[1-(2,2,2-Trifluoroacetyl)azetidin-3-yl]oxy}benzoic acid
  • 2-[3-Acetyl-2-(trifluoromethyl)-2,3-dihydro-1,3-benzoxazol-2-yl]acetic acid
  • 3,3-Difluoro-1-(2-methoxy-3-methylphenyl)cyclobutan-1-amine
  • benzyl N-{1-[5-(hydroxymethyl)-1,3,4-thiadiazol-2-yl]ethyl}carbamate
  • rel-(2R)-2-(N-{5,6-dimethylthieno[2,3-d]pyrimidin-4-yl}acetamido)propanoic acid
  • (4,5,6,7-Tetrahydro-1-benzothiophen-3-yl)methanesulfonyl chloride
  • benzyl N-{[5-(hydroxymethyl)-1,3,4-thiadiazol-2-yl]methyl}-N-methylcarbamate
  • benzyl N-(4,6-disulfanylpyrimidin-5-yl)carbamate