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
  • (4-ethoxyphenyl)[6-fluoro-4-(4-isopropylphenyl)-1,1-dioxido-4H-1,4-benzothiazin-2-yl]methanone
  • 3-Chloro-4-(methylamino)benzaldehyde
  • N-Ethyl-4-(2-pyridinyl)-1-piperazinecarboxamide
  • O-Oxalylhomoserine
  • (2S,3S,5R,6R)-3-[2-[3-[[(2R)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-6-(2-hydroxypropan-2-yl)-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
  • cyclo-dopa 5-O-glucoside
  • N-(1,3-Benzodioxol-5-Ylmethyl)-1-[(1r)-1-Naphthalen-1-Ylethyl]piperidine-4-Carboxamide
  • 1-(3-Methylphenyl)-4-(4,5,6,7-tetrahydro-1-benzothiophene-2-carbonyl)piperazine
  • N-[2-(1H-1,3-benzimidazol-1-yl)ethyl]-4-(2-pyrimidinylamino)butanamide
  • 2-(2-methyl-1H-indol-3-yl)-N-((5-methylisoxazol-3-yl)methyl)-2-oxoacetamide
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