Methyl (4-hydroxymethyl)benzoate

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Names

[ CAS No. ]:
6908-41-4

[ Name ]:
Methyl (4-hydroxymethyl)benzoate

[Synonym ]:
methyl 4-(hydroxymethyl)benzoate
EINECS 230-017-0
MFCD00009984

Chemical & Physical Properties

[ Density]:
1.177g/cm3

[ Boiling Point ]:
157 °C / 5mmHg

[ Melting Point ]:
47-50 °C(lit.)

[ Molecular Formula ]:
C9H10O3

[ Molecular Weight ]:
166.17400

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
166.06300

[ PSA ]:
46.53000

[ LogP ]:
0.96550

[ Index of Refraction ]:
1.542

MSDS

Click to get detail MSDS

Safety Information

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

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S37/39-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2918199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Methyl 4-formylbenzoate
  • Methyl 4-(chlorocarbonyl)benzoate
  • mono-methyl_terephthalate
  • DMT
  • methyl 4-((phenylthio)carbonyl)benzoate
  • methyl 4-[(tetrahydropyran-2-yloxy)methyl]benzoate
  • Methanol
  • 4-(Hydroxymethyl)benzoic acid
  • Methyl 4-(bromomethyl)benzoate

DownStream

  • methyl 4-[(4-nitrophenoxy)carbonyloxymethyl]benzoate
  • Methyl 4-(chloromethyl)benzoate
  • methyl p-toluate
  • Methyl benzoate
  • Benzoic acid, 4-[phenylimino)-,methyl ester
  • 4-(Acetoxymethyl)benzoic acid methyl ester
  • 4-(Hydroxymethyl)benzoic acid
  • Methyl 4-formylbenzoate
  • Methanol
  • methyl 4-ethynylbenzoate

Customs

[ HS Code ]: 2918199090

[ Summary ]:
2918199090 other carboxylic acids with alcohol function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Evolution, synthesis and SAR of tripeptide alpha-ketoacid inhibitors of the hepatitis C virus NS3/NS4A serine protease.

Bioorg. Med. Chem. Lett. 12(4) , 705-8, (2002)

N-terminal truncation of the hexapeptide ketoacid 1 gave rise to potent tripeptide inhibitors of the hepatitis C virus NS3 protease/NS4A cofactor complex. Optimization of these tripeptides led to keto...


More Articles

Related Compounds

  • methyl 4-bromo-3-(hydroxymethyl)benzoate
  • methyl 4-[(E)-(2,4-dioxo-1H-quinolin-3-ylidene)-hydroxymethyl]benzoate
  • methyl 4-[(3,4,5,6,7,8-hexahydro-5,5,8,8-tetramethyl-1(2H)-oxoanthracen-2-yl)hydroxymethyl]benzoate
  • methyl 4-(hydroxymethyl)norbornane-1-carboxylate
  • methyl 4-hydroxymethyl-1-triphenylmethylimidazole-5-carboxylate
  • methyl 4-(hydroxymethyl)-1H-pyrrole-2-carboxylate
  • [1-(2-Methoxy-4,5-dimethylphenyl)-2,2-dimethylcyclopropyl]methanamine
  • 1-methyl-5-[1-(2-methylpropyl)-1H-pyrazol-3-yl]-1H-pyrazol-4-amine
  • 1-[(3,4,5-Trifluorophenyl)methyl]cyclopropan-1-ol
  • {1-[(2-Methylquinolin-6-yl)methyl]cyclopropyl}methanol
  • 2-[1-(Aminomethyl)-2,2-dimethylcyclopropyl]-5-bromophenol
  • 1-{[2-chloro-5-(trifluoromethyl)phenyl]methyl}-N-methylcyclopropan-1-amine
  • Methyl({2-[5-(trifluoromethyl)pyridin-2-yl]propan-2-yl})amine
  • methyl (3R)-3-[4-(dimethylamino)-3-fluorophenyl]-3-hydroxypropanoate
  • Tert-butyl 3-[1-(aminooxy)-2-methylpropan-2-yl]piperidine-1-carboxylate
  • 4-Amino-3-(5-chloro-2-fluoropyridin-3-yl)butanoic acid
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