METHYL 3-METHOXYACRYLATE
METHYL 3-METHOXYACRYLATE Basic information
- Product Name:
- METHYL 3-METHOXYACRYLATE
- Synonyms:
-
- Methyl trans-3-methoxyacrylate,95%
- Methyl 3-methoxyacrylate
- (E)-Methyl 3-Methoxyacrylate
- Methyl trans-3-Methoxyacrylate 97%
- Methyl trans-3-methoxyacrylate
- 2-Propenoic acid,3-methoxy-, methyl ester, (2E)-
- trans-3-methoxyacrylate
- METHYL TRANS-3-METHOXYACRYLATE
- CAS:
- 5788-17-0
- MF:
- C5H8O3
- MW:
- 116.12
- EINECS:
- 412-900-4
- Product Categories:
-
- C2 to C5
- Carbonyl Compounds
- Esters
- Mol File:
- 5788-17-0.mol
METHYL 3-METHOXYACRYLATE Chemical Properties
- Melting point:
- 3-4 °C
- Boiling point:
- 56 °C18 mm Hg(lit.)
- Density
- 1.08 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.451(lit.)
- Flash point:
- 145 °F
- storage temp.
- 2-8°C
- form
- liquid
- Appearance
- Colorless to light yellow Liquid
- InChI
- InChI=1S/C5H8O3/c1-7-4-3-5(6)8-2/h3-4H,1-2H3/b4-3+
- InChIKey
- AUTCCPQKLPMHDN-ONEGZZNKSA-N
- SMILES
- C(OC)(=O)/C=C/OC
- CAS DataBase Reference
- 5788-17-0
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
METHYL 3-METHOXYACRYLATE Usage And Synthesis
Chemical Properties
CLEAR COLOURLESS LIQUID
Uses
Methyl trans-3-methoxyacrylate may be used in the preparation of:
- 5- hydroxyquinolines
- 7-hydroxyquinolines
- methyl 5-methoxyquinoline-3-carboxylate
Synthesis
Method 1: Starting from vinyl methyl ether and single phosgene in the presence of solvent and catalyst addition reaction to produce chloride and propionyl chloride, propionyl chloride and methanol in the presence of organic base substitution condensation to produce chlorinated alkyl esters, alkyl esters and then in the presence of catalyst for cracking reaction, off HCl, to get 3-methoxyacrylic acid methyl ester.
Method 2: Methyl acrylate is used as raw material, 2,3-dibromopropionic acid methyl ester is obtained by bromination and addition, and then 3,3-dimethoxypropionic acid methyl ester is obtained by etherification with sodium methanol, and then cracking reaction is carried out under the presence of catalyst, and HCl is taken off, and then 3-methoxyacrylic acid methyl ester is obtained.
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