Methyl 3-methoxypent-2-enoate

Base Information

• Chemical Name: Methyl 3-methoxypent-2-enoate
• CAS No.: 104065-67-0
• Molecular Formula: C7H12 O3
• Molecular Weight: 144.17
• Hs Code.: 2918990090
• DSSTox Substance ID: DTXSID30363534
• Mol file: 104065-67-0.mol

Synonyms:Methyl 3-methoxypent-2-enoate;3-Methoxy-2-pentenoic Acid Methyl Ester;104065-67-0;METHYL 3-METHOXY-2-PENTENOATE;DTXSID30363534;(E)-methyl 3-methoxypent-2-enoate;AKOS030255025;FT-0695103

Chemical Property of Methyl 3-methoxypent-2-enoate

Chemical Property:

• Vapor Pressure: 0.595mmHg at 25°C
• Refractive Index: 1.427
• Boiling Point: 188.6°Cat760mmHg
• Flash Point: 69.3°C
• PSA: 35.53000
• Density: 0.978g/cm³
• LogP: 1.09970
• XLogP3: 1.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 144.078644241
• Heavy Atom Count: 10
• Complexity: 138

Purity/Quality:

97% ^*data from raw suppliers

3-Methoxy-2-pentenoicAcidMethylEster ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(=CC(=O)OC)OC
• Uses: 3-Methoxy-2-pentenoic Acid Methyl Ester is an intermediate in the synthesis of prostaglandins.

Technology Process of Methyl 3-methoxypent-2-enoate

There total 2 articles about Methyl 3-methoxypent-2-enoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 64.0%

methyl propanoyl acetate (30414-53-0) + trimethyl orthoformate (149-73-5) → methyl 3-methoxypent-2-enoate (104065-67-0)

Guidance literature:

With sulfuric acid; at 0 - 20 ℃; for 24h;

DOI:10.1039/c3cc47800a

Reference yield:

concentrated H2 SO4 + methyl propanoyl acetate (30414-53-0) → 3-methoxy-2-pentenoic acid methyl ester (104065-67-0)

Guidance literature:

With trimethyl orthoformate;

Reference yield:

5-benzyloxy-3-(2-hydroxyethyl)indole (41339-61-1) + 3-methoxy-2-pentenoic acid methyl ester (104065-67-0) → 1-Ethyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-acetic acid methyl ester (135873-13-1)

Guidance literature:

With trifluoroborane diethyl ether; In dichloromethane; ethyl acetate;

upstream raw materials:

methyl propanoyl acetate

trimethyl orthoformate

Downstream raw materials:

1-Ethyl-1,3,4,9-tetrahydro-6-(phenylmethoxy)pyrano[3,4-b]indole-1-acetic acid methyl ester

(2'R,3'R)-1-benzyl-5-bromo-4'-methoxy-3'-methylspiro[indoline-3,2'-pyran]-2,6'(3'H)-dione

(2'R,3'R)-1-benzyl-5-fluoro-4'-methoxy-3'-methylspiro[indoline-3,2'-pyran]-2,6'(3'H)-dione

(2'R,3'R)-1-benzyl-5-chloro-4'-methoxy-3'-methylspiro[indoline-3,2'-pyran]-2,6'(3'H)-dione

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