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Methyl 3-methoxypropionate

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Methyl 3-methoxypropionate Basic information
Preparation
Product Name:Methyl 3-methoxypropionate
Synonyms:Methyl β-Methoxypropionate;Methyl 3-methoxypropionate,98%;Methyl 3-methoxyprop;3-Methoxy propionate;Methyl 3-methoxypropiote;METHYL 3-METHOXYPROPIONATE;METHYL 3-METHOXYPROPIONATE, 99+%;Methylmethoxypropanoate
CAS:3852-09-3
MF:C5H10O3
MW:118.13
EINECS:223-358-1
Product Categories:Aromatic Propionic Acids;C2 to C5;Carbonyl Compounds;Esters;3852-09-3
Mol File:3852-09-3.mol
Methyl 3-methoxypropionate Structure
Methyl 3-methoxypropionate Chemical Properties
Boiling point 142-143 °C (lit.)
density 1.009 g/mL at 25 °C (lit.)
vapor pressure 9.733-15.999hPa at 20-25℃
refractive index n20/D 1.402(lit.)
Fp 118 °F
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Colorless to Almost colorless
Specific Gravity1.013 (20℃)
Water Solubility 428.60g/L(25 ºC)
BRN 1744829
InChIInChI=1S/C5H10O3/c1-7-4-3-5(6)8-2/h3-4H2,1-2H3
InChIKeyBDJSOPWXYLFTNW-UHFFFAOYSA-N
SMILESC(OC)(=O)CCOC
LogP0.1
CAS DataBase Reference3852-09-3(CAS DataBase Reference)
EPA Substance Registry SystemPropanoic acid, 3-methoxy-, methyl ester (3852-09-3)
Safety Information
Hazard Codes Xi
Risk Statements 10-36/37/38
Safety Statements 26-36-37/39
RIDADR UN 3272 3/PG 3
WGK Germany 3
RTECS UF5274000
TSCA TSCA listed
HazardClass 3.2
PackingGroup III
HS Code 29189900
Storage Class3 - Flammable liquids
Hazard ClassificationsEye Irrit. 2
Flam. Liq. 3
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
Methyl 3-methoxypropionate English
ACROS English
SigmaAldrich English
Methyl 3-methoxypropionate Usage And Synthesis
PreparationIn a dry reaction flask, 0.2 mL of Na₂CO₃ (0.05 M aq.) was added to a solution of ethyl acrylate (0.5 mmol) and methanol (2.0 mmol). The resulting reaction mixture was stirred at room temperature for approximately 5 hours until the olefins were completely consumed. The reaction progress was monitored by thin-layer chromatography (TLC). After the reaction was complete, the reaction mixture was extracted three times with ethyl acetate (3 x 5 mL). The combined organic layers were washed with brine (10 mL) and dried over Na₂SO₄. The organic layers were filtered to remove the drying agent, and the resulting organic solvent was concentrated under vacuum. The crude product was purified by silica gel column chromatography (eluent: PE: EtOAc = 8:1) to obtain methyl 3-methoxypropionate.
Chemical Propertiesclear colorless liquid
UsesMethyl 3-methoxypropionate may be employed as acylation reagent for the lipase-catalyzed N-acylation of 1-phenylethanamine. It may be used in the synthesis of poly(2-hydroxylethyl 5-norbornene-2-carboxylate /t-butyl 5-norbornene-2-carboxylate /5-norbornene-2-carboxylic acid /maleic anhydride) resists. Lithographic performance of these resists was studied using ArF stepper.
Synthesis Reference(s)Journal of the American Chemical Society, 68, p. 544, 1946 DOI: 10.1021/ja01208a003
General DescriptionMethyl 3-methoxypropionate is an ester.
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