3-Decen-1-ol, (Z)-

Base Information

• Chemical Name: 3-Decen-1-ol, (Z)-
• CAS No.: 10340-22-4
• Molecular Formula: C10H20O
• Molecular Weight: 156.268
• Hs Code.: 2905290000
• European Community (EC) Number: 233-734-7
• UNII: A00BN8C8CC
• DSSTox Substance ID: DTXSID00884463
• Nikkaji Number: J82.052K
• Metabolomics Workbench ID: 3229
• Mol file: 10340-22-4.mol

Synonyms:10340-22-4;3-Decen-1-ol, (Z)-;(Z)-3-Decenol;(Z)-dec-3-en-1-ol;3-Decen-1-ol, (3Z)-;(3Z)-3-Decen-1-ol;cis-3-Decen-1-Ol;(Z)-3-decen-1-ol;3-Dedecen-1-ol, (Z)-;3Z-Decen-1-ol;UNII-A00BN8C8CC;A00BN8C8CC;EINECS 233-734-7;cis-Slaterol;SCHEMBL3498336;DTXSID00884463;MTIJDFJGPCJFKE-FPLPWBNLSA-N;(3Z)-DEC-3-EN-1-OL;LMFA05000139;Q27273442

Chemical Property of 3-Decen-1-ol, (Z)-

Chemical Property:

• Vapor Pressure: 0.0128mmHg at 25°C
• Refractive Index: 1.453
• Boiling Point: 230.1 °C at 760 mmHg
• PKA: 14.92±0.10(Predicted)
• Flash Point: 86.5 °C
• PSA: 20.23000
• Density: 0.845 g/cm³
• LogP: 2.89540
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 7
• Exact Mass: 156.151415257
• Heavy Atom Count: 11
• Complexity: 86.9

Purity/Quality:

95% ^*data from raw suppliers

(3Z)-Decen-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCC=CCCO
• Isomeric SMILES: CCCCCC/C=C\CCO
• Uses: (3Z)-Decen-1-ol can be used as reactant/reagent in studies of influence of the Chemical Structure on Odor Qualities and Odor Thresholds in Homologous Series of Alka-1,5-dien-3-ones, Alk-1-en-3-ones, Alka-1,5-dien-3-ols, and Alk-1-en-3-ols.

Technology Process of 3-Decen-1-ol, (Z)-

There total 7 articles about 3-Decen-1-ol, (Z)- 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: 94.0%

3-decyn-1-ol (51721-39-2) → (Z)-dec-3-en-1-ol (10340-22-4)

Guidance literature:

With 5% palladium on barium sulphate; hydrogen; In pyridine; at 20 ℃; for 12h; Sealed tube;

Reference yield: 82.0%

(Z)-1-(2-tetrahydropyranyloxy)-dec-3-ene (137103-87-8) → (Z)-dec-3-en-1-ol (10340-22-4)

Guidance literature:

With toluene-4-sulfonic acid; In methanol; for 6h; Ambient temperature;

Reference yield: 47.0%

2,3-dihydro-2H-furan (1191-99-7,75454-45-4) + n-hexylmagnesium bromide (3761-92-0) → (Z)-dec-3-en-1-ol (10340-22-4)

Guidance literature:

2,3-dihydro-2H-furan; With bis(1,5-cyclooctadiene)nickel⁽⁰⁾; C₂₇H₃₉N₂⁽¹⁺⁾*Cl^(1-)*ClH; lithium chloride; In tetrahydrofuran; at -30 ℃; for 0.0333333h; Inert atmosphere;

n-hexylmagnesium bromide; In tetrahydrofuran; at -30 ℃; for 16h; stereoselective reaction; Inert atmosphere;

DOI:10.1021/ol4031815

upstream raw materials:

heptanal

3-hydroxypropyltriphenylphosphonium bromide

3-decyn-1-ol

(Z)-1-(2-tetrahydropyranyloxy)-dec-3-ene

Downstream raw materials:

1-((Z)-9-Isocyano-nonadec-12-ene-9-sulfonyl)-4-methyl-benzene

1-((Z)-10-Isocyano-icos-13-ene-10-sulfonyl)-4-methyl-benzene

Refernces

• 1、 D’yakonov, Vladimir A.,Makarov, Alexey A.,Dzhemileva, Lilya U.,Ramazanov, Ilfir R.,Makarova, Elina Kh.,Dzhemilev, Usein M.. "Natural trienoic acids as anticancer agents: First stereoselective synthesis, cell cycle analysis, induction of apoptosis, cell signaling and mitochondrial targeting studies". . . Retrieved 2021.
• 2、 -. "CYCLOALKYL-CONTAINING CARBOXYLIC ACIDS AND USES THEREOF". Page/Page column 73; 75. . Retrieved 2021/06/26.
• 3、 Wissing, Maren,Niehues, Maximilian,Ravoo, Bart Jan,Studer, Armido. "Synthesis and Immobilization of Metal Nanoparticles Using Photoactive Polymer-Decorated Zeolite L Crystals and Their Application in Catalysis". supporting information. p. 2245 - 2253. Retrieved 2020/05/05.