4-Hexenoic acid, methyl ester, (4E)-

Base Information

Chemical Name:4-Hexenoic acid, methyl ester, (4E)-
CAS No.:14017-81-3
Molecular Formula:C7H12O2
Molecular Weight:128.171
Hs Code.:
Mol file:14017-81-3.mol

Synonyms:Methyl (4E)-hex-4-enoate;4-Hexenoic acid, methyl ester, (E)- (8CI);Methyl trans-4-hexenoate;

Suppliers and Price of 4-Hexenoic acid, methyl ester, (4E)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 9 raw suppliers

Chemical Property of 4-Hexenoic acid, methyl ester, (4E)-

Chemical Property:

Boiling Point:126 °C at 760 mmHg
Flash Point:40.1 °C
Density:0.907 g/cm³

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4-Hexenoic acid, methyl ester, (4E)-

There total 3 articles about 4-Hexenoic acid, methyl ester, (4E)- 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:

: 1918-79-2
2-methylthiophene-5-carboxylic acid

: 689-89-4
(2E,4E)-methylhexa-2,4-dienoate

: 71624-92-5
Methyl 2,5-Dihydro-5-methyl-2-thiophenecarboxylate

: 13894-61-6
methyl (E)-hex-3-enoate

: 14017-81-3
methyl (E)-hex-4-enoate

: 13894-62-7
methyl (Z)-hex-3-enoate

: 86610-45-9
Methyl (Z)-5-Mercapto-3-hexenoate

Guidance literature:: With methanol; sulfuric acid; ammonia; lithium; Product distribution; Mechanism; 1) -78 degC, 60 min, 2) room temp., 24 h; other amount of Li: 10 eq.;
DOI:10.1021/jo00167a013

Reference yield:

: 67-56-1
methanol

: 124-38-9,18923-20-1
carbon dioxide

: 1567-14-2
methyl (2E)-2-methyl-2-pentenoate

: 13894-61-6
methyl (E)-hex-3-enoate

: 14017-81-3
methyl (E)-hex-4-enoate

Guidance literature:: With hydrogenchloride; Yield given. Multistep reaction. Yields of byproduct given; 1.) 3 d, 35 deg C, THF;
DOI:10.1016/0022-328X(87)85007-6

Reference yield:

: 35194-36-6
hex-4-enoic acid

: 74-88-4
methyl iodide

: 14017-81-3
methyl (E)-hex-4-enoate

: 13894-60-5
methyl (Z)-hex-4-enoate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 2h; Title compound not separated from byproducts;
DOI:10.1021/ol036062m