407429
Methyl 3-methoxypropionate
≥99%
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About This Item
Linear Formula:
CH3OCH2CH2COOCH3
CAS Number:
Molecular Weight:
118.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-358-1
Beilstein/REAXYS Number:
1744829
MDL number:
Assay:
≥99%
Form:
liquid
InChI key
BDJSOPWXYLFTNW-UHFFFAOYSA-N
InChI
1S/C5H10O3/c1-7-4-3-5(6)8-2/h3-4H2,1-2H3
SMILES string
COCCC(=O)OC
assay
≥99%
form
liquid
Quality Level
bp
142-143 °C (lit.)
density
1.009 g/mL at 25 °C (lit.)
functional group
ester, ether
Related Categories
General description
Methyl 3-methoxypropionate is an ester.
Application
Methyl 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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
116.6 °F - closed cup
flash_point_c
47 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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A Novel Alicyclic Polymers for 193nm Single Layer Resist Materials
Jung J-C, et al.
J. Photopolym. Sci. Technol., 11(3), 481-488 (1998)
Maria Cammenberg et al.
Chembiochem : a European journal of chemical biology, 7(11), 1745-1749 (2006-09-23)
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 al. used ethyl methoxyacetate instead of ethyl butyrate as an acylation reagent for the
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