Methyl 4-methoxybutanoate

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Names

[ CAS No. ]:
29006-01-7

[ Name ]:
Methyl 4-methoxybutanoate

[Synonym ]:
MFCD00274316
4-Methoxy-buttersaeure-methylester
methyl,4-Methoxybutanoate
Butyric acid,4-methoxy-,methyl ester
4-methoxybutyric acid methyl ester
methyl 4-methoxybutyrate
methyl methoxybutyrate

Chemical & Physical Properties

[ Density]:
0.961

[ Boiling Point ]:
155ºC

[ Molecular Formula ]:
C6H12O3

[ Molecular Weight ]:
132.15800

[ Flash Point ]:
48ºC

[ Exact Mass ]:
132.07900

[ PSA ]:
35.53000

[ LogP ]:
0.58600

[ Vapour Pressure ]:
3.1mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.408(lit.)

MSDS

Safety Information

[ Symbol ]:

GHS02

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H226

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
F+

[ Risk Phrases ]:
10

[ Safety Phrases ]:
16

[ RIDADR ]:
UN 3272 3/PG 3

[ HS Code ]:
2918990090

Synthetic Route

Precursor & DownStream

Precursor

  • gamma-Butyrolactone
  • Trimethyl orthoformate
  • Methanol
  • 1-iodo-3-methoxypropane
  • carbon monoxide
  • 4-Methoxybutanoic acid
  • Oxetane
  • Carbon dioxide
  • methyl iodide
  • diazomethane

DownStream

  • 4-Methoxy-4-oxobutanoic acid
  • Dimethyl succinate
  • 4-Methoxybutanoic acid
  • 1,5-Pentanediol
  • 7-methoxy-1-hepten-4-ol
  • 4-Methoxybutanal
  • 1-dimethoxyphosphoryl-5-methoxypentan-2-one

Customs

[ HS Code ]: 2918990090

[ Summary ]:
2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Molecular basis for the enhanced lipase-catalyzed N-acylation of 1-phenylethanamine with methoxyacetate.

ChemBioChem. 7(11) , 1745-9, (2006)

One of the commercial methods for preparing enantiopure amines is lipase-catalyzed kinetic resolution, although lipases catalyze aminolysis with only low activity. Interestingly, in 1997 Balkenhohl et...

Systematic evaluation of the conformational properties of aliphatic omega-methoxy methyl esters.

J. Org. Chem. 70(19) , 7731-6, (2005)

[structure: see text] A systematic conformational study of omega-methoxy methyl esters, CH(3)O-(CH2)n-COO-CH3 with n = 3 and 4, has been performed using quantum mechanical calculations at the MP2 leve...


More Articles


Related Compounds

  • methyl 4-imino-4-methoxybutanoate
  • methyl 4-chloro-3-methoxybutanoate
  • methyl 4,4-difluoro-3-hydroxy-3-methoxybutanoate
  • methyl 2-(benzo[d]thiazol-2-ylthio)-4-methoxybutanoate
  • methyl 4-(hydroxymethyl)-1H-pyrrole-2-carboxylate
  • methyl 4,5-dipropyl-1H-pyrrole-2-carboxylate
  • 1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-3-(1-(4-methoxyphenyl)-5-oxopyrrolidin-3-yl)urea
  • 1-(3-Chloro-2-methylphenyl)-3-[1-(4-methoxyphenyl)-5-oxopyrrolidin-3-yl]urea
  • 1-(5-Chloro-2-methylphenyl)-3-[1-(4-methoxyphenyl)-5-oxopyrrolidin-3-yl]urea
  • 1-(3-Fluoro-4-methylphenyl)-3-[1-(4-methoxyphenyl)-5-oxopyrrolidin-3-yl]urea
  • 1-(1-(4-Methoxyphenyl)-5-oxopyrrolidin-3-yl)-3-(pyridin-3-yl)urea
  • 1-[2-(1H-indol-3-yl)ethyl]-3-[1-(4-methoxyphenyl)-5-oxopyrrolidin-3-yl]urea
  • N-(3-(3-(1-(4-methoxyphenyl)-5-oxopyrrolidin-3-yl)ureido)phenyl)acetamide
  • N-(4-(3-(1-(4-methoxyphenyl)-5-oxopyrrolidin-3-yl)ureido)phenyl)acetamide
  • 1-(1-(4-methoxyphenyl)-5-oxopyrrolidin-3-yl)-3-((2-methyl-1H-indol-5-yl)methyl)urea
  • N-(2-(3-(1-(4-methoxyphenyl)-5-oxopyrrolidin-3-yl)ureido)ethyl)acetamide
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