3Z-nonenoic acid

Base Information

Chemical Name:3Z-nonenoic acid
CAS No.:41653-98-9
Molecular Formula:C9H16O2
Molecular Weight:156.225
Hs Code.:
UNII:2PH40QU00W
Nikkaji Number:J98.033A
Wikidata:Q27255417
Metabolomics Workbench ID:854
Mol file:41653-98-9.mol

Synonyms:3Z-nonenoic acid;cis-3-Nonenoic acid;3-Nonenoic acid, (Z)-;3-Nonenoic acid, (3Z)-;UNII-2PH40QU00W;2PH40QU00W;41653-98-9;C9:1n-6;(Z)-non-3-enoic acid;(Z)-3-Nonenoic acid;xi-3-Nonenoic acid;(3Z)-3-nonenoic acid;SCHEMBL5370778;ZBPYTVBKHKUNHG-SREVYHEPSA-N;LMFA01030444;Q27255417

Suppliers and Price of 3Z-nonenoic 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
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price

Total 0 raw suppliers

Chemical Property of 3Z-nonenoic acid

Chemical Property:

PSA：37.30000
LogP:2.59760
XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:156.115029749
Heavy Atom Count:11
Complexity:128

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCC=CCC(=O)O
Isomeric SMILES:CCCCC/C=C\CC(=O)O

Technology Process of 3Z-nonenoic acid

There total 17 articles about 3Z-nonenoic 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:

: 60-33-3,116745-32-5,26085-09-6,64080-88-2,7049-66-3,949900-18-9,60476-23-5,6144-28-1,67922-65-0,89718-18-3
linoleic acid

: 3788-56-5
9-hydroxynonanoic acid

: 41653-98-9,4124-88-3
(Z)-non-3-enoic acid

Guidance literature:: With recombinant escherichia coli BL₂₁(DE₃) expressing alcohol dehydrogenase from micrococcus luteus NCTC₂₆₆₅, Baeyer-Villiger monooxygenase from pseudomonas putida KT₂₄₄₀, oleate hydratase of stenotrophomonas maltophilia; In aq. buffer; at 35 ℃; pH=8; Overall yield = > 50 %; Microbiological reaction;
DOI:10.1002/anie.201209187

Reference yield:

: 3391-86-4
1-octen-3-ol

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

: 28163-88-4,4124-88-3
(E)-non-3-enoic acid

: 41653-98-9,4124-88-3
(Z)-non-3-enoic acid

Guidance literature:: With nickel(II) bromide dimethoxyethane; Bathocuproine; magnesium chloride; zinc; In N,N-dimethyl-formamide; at 40 ℃; for 40h; under 760.051 Torr; Overall yield = 63 %; Overall yield = 24.6 mg; diastereoselective reaction; Schlenk technique; Glovebox;
DOI:10.1002/anie.201702857

Reference yield:

: 201230-82-2
carbon monoxide

: 147583-38-8
1-vinyl hexyl diethyl phosphate

: 28163-88-4,4124-88-3
(E)-non-3-enoic acid

: 41653-98-9,4124-88-3
(Z)-non-3-enoic acid

Guidance literature:: With hexarhodium hexadecacarbonyl; tetrabutyl-ammonium chloride; water; triethylamine; In dimethyl sulfoxide; at 50 ℃; for 10h; under 15200 Torr; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1016/0022-328X(93)83025-Q