(Z)-8-DODECEN-1-YL ACETATE

Base Information

• Chemical Name: (Z)-8-DODECEN-1-YL ACETATE
• CAS No.: 28079-04-1
• Molecular Formula: C14H26O2
• Molecular Weight: 226.359
• Hs Code.: 2915390090
• European Community (EC) Number: 248-823-6
• UNII: 0MWD335OTN
• DSSTox Substance ID: DTXSID9035543
• Nikkaji Number: J4.090H
• Wikidata: Q27236972
• Metabolomics Workbench ID: 3890
• Mol file: 28079-04-1.mol

Synonyms:8-Dodecen-1-ol,acetate, (8Z)- (9CI);8-Dodecen-1-ol, acetate, (Z)- (8CI);(8Z)-Dodec-8-en-1-olacetate;(Z)-8-Dodecen-1-ol acetate;(Z)-8-Dodecen-1-yl acetate;(Z)-8-Dodecenyl acetate;Denacil;Funemone;GM;Orfamone;cis-8-Dodecen-1-yl acetate;8-Dodecen-1-ol,1-acetate, (8Z)-;

Chemical Property of (Z)-8-DODECEN-1-YL ACETATE

Chemical Property:

• Vapor Pressure: 0.00114mmHg at 25°C
• Refractive Index: 1.448
• Boiling Point: 300.1 °C at 760 mmHg
• Flash Point: 96.5 °C
• PSA: 26.30000
• Density: 0.881 g/cm³
• LogP: 4.24640
• Storage Temp.: 2-8°C
• Solubility.: DMSO (Slightly), Water (Slightly)
• XLogP3: 4.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 11
• Exact Mass: 226.193280068
• Heavy Atom Count: 16
• Complexity: 185

Purity/Quality:

93% ^*data from raw suppliers

GentamicinDeuterated(CComplex)PentaacetateSalt(Containsd0) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCC=CCCCCCCCOC(=O)C
• Isomeric SMILES: CCC/C=C\CCCCCCCOC(=O)C
• Uses: Inhibits protein synthesis by binding to L6 protein of 50S ribosomal subunit. Antibacterial. Antibiotic complex consists of three closely related components, gentamicins C1, C2, C1a, and also gentamic in A which differs from the other members of the complex but is similar to Kanamycin C. Gentamicin C1: R1=R2=CH3 Gentamicin C2: R1=CH3; R2=H Gentamicin C1A: R1=R2=H (8Z)-Dodecenyl Acetate is derived from 1-Pentyne (P284800), which is used as a reagent in the synthesis of novel 1,2,3-triazole-1,4-benzoxazine hybrids which exhibit antiproliferative activity. 1-Pentyne is also used as a reagent in the synthesis of disubstituted isoxazoles which exhibit anti-aging activity.

Technology Process of (Z)-8-DODECEN-1-YL ACETATE

There total 76 articles about (Z)-8-DODECEN-1-YL ACETATE 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: 97.0%

1-Acetoxydodec-8-yne (26906-26-3) → (Z)-8-dodecen-1-yl acetate (28079-04-1)

Guidance literature:

With quinoline; hydrogen; Pd-BaSO₄; In methanol;

Reference yield: 95.0%

Δ8-dodecen-1-ol (153123-34-3) + acetic anhydride (108-24-7) → (Z)-8-dodecen-1-yl acetate (28079-04-1)

Guidance literature:

With pyridine; at 5 - 25 ℃; for 2h; Large scale;

Reference yield: 95.0%

(Z)-8-dodecenol (40642-40-8) + acetyl chloride (75-36-5) → (Z)-8-dodecen-1-yl acetate (28079-04-1)

Guidance literature:

In pyridine;

upstream raw materials:

(E)-8-dodecenyl acetate

(Z)-8-dodecenol

acetyl chloride

1-Acetoxydodec-8-yne

Refernces

• 1、 Babler,Coghlan. "". . p. 1971. Retrieved 1979.
• 2、 -. "SYNTHESIS OF PHEROMONE DERIVATIVES VIA Z-SELECTIVE OLEFIN METATHESIS". Paragraph 0261; 0267. . Retrieved 2021/12/28.
• 3、 -. "Synthesis method of (Z/E)-8-dodecen-1-alcohol acetate compound". . . Retrieved 2019/05/21.