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
Quality Level
assay
≥99%
form
liquid
refractive index
n20/D 1.402 (lit.)
bp
142-143 °C (lit.)
density
1.009 g/mL at 25 °C (lit.)
functional group
ester, ether
SMILES string
COCCC(=O)OC
InChI
1S/C5H10O3/c1-7-4-3-5(6)8-2/h3-4H2,1-2H3
InChI key
BDJSOPWXYLFTNW-UHFFFAOYSA-N
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 407429-250ML | 04061831988192 |
| 407429-1L | 04061836692209 |