(2E,4Z)-hexa-2,4-dienoic acid

Base Information

Chemical Name:(2E,4Z)-hexa-2,4-dienoic acid
CAS No.:30361-30-9
Molecular Formula:C₆H₈O₂
Molecular Weight:112.128
Hs Code.:
NSC Number:50268,49103
DSSTox Substance ID:DTXSID301309200
Nikkaji Number:J1.452.131C
Wikidata:Q27117557
Metabolomics Workbench ID:55840
Mol file:30361-30-9.mol

Synonyms:(2E,4Z)-hexa-2,4-dienoic acid;30361-30-9;(2E,4Z)-2,4-hexadienoic acid;2,4-Hexadienoic acid, (2E,4Z)-;(2E,4Z)-sorbic acid;(2E,4Z)-SA;NSC49103;SCHEMBL5374461;CHEBI:38361;DTXSID301309200;NSC50268;(2E, 4Z)-2, 4-hexadienoic acid;AKOS037645338;2-trans,4-cis-hexa -2,4-dienoic acid;AS-60253;D86563;A930221;EN300-22861890;Q27117557

Suppliers and Price of (2E,4Z)-hexa-2,4-dienoic acid

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

TRC
trans,cis-Sorbicacid
250mg
$ 1695.00

TRC
trans,cis-Sorbicacid
100mg
$ 765.00

TRC
trans,cis-Sorbicacid
50mg
$ 405.00

Total 4 raw suppliers

Chemical Property of (2E,4Z)-hexa-2,4-dienoic acid

Chemical Property:

Melting Point:35-38 °C(Solv: pentane (109-66-0))
Boiling Point:58 - 60 °C (0.05 mmHg)
PSA：37.30000
Density:1.024±0.06 g/cm3(Predicted)
LogP:1.20330
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:112.052429494
Heavy Atom Count:8
Complexity:123

Purity/Quality:

99% ^*data from raw suppliers

trans,cis-Sorbicacid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC=CC=CC(=O)O
Isomeric SMILES:C/C=C\C=C\C(=O)O
Uses trans,cis-Sorbic acid has been used in the study of photosensitization of carbon nanotubes and the production of reactive oxygen species by using the sorbic acid as a catalyst in the reaction process.

Technology Process of (2E,4Z)-hexa-2,4-dienoic acid

There total 24 articles about (2E,4Z)-hexa-2,4-dienoic acid 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: 79.0%

: 4423-18-1
(but-2-enylidene)malonic acid

: 110-44-1,5309-56-8,5309-57-9,22500-92-1,30361-30-9,91751-55-2
(2Z,4E)-hexa-2,4-dienoic acid

Guidance literature:: With quinoline; at 130 ℃; for 3h;
DOI:10.1021/ja020635t

Reference yield: 54.0%

: 3-butenoic acid 1-methyl-2-propen-1-yl ester

: 110-44-1,5309-56-8,5309-57-9,22500-92-1,30361-30-9,91751-55-2
(2Z,4E)-hexa-2,4-dienoic acid

Guidance literature:: With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; sodium hydride; In toluene; mineral oil; at 65 ℃; for 4.5h;
DOI:10.1002/anie.202106250