8-Nonenyl Acetate

Base Information

• Chemical Name: 8-Nonenyl Acetate
• CAS No.: 13038-22-7
• Molecular Formula: C11H20 O2
• Molecular Weight: 184.279
• European Community (EC) Number: 844-776-6
• DSSTox Substance ID: DTXSID10576680
• Nikkaji Number: J118.230G
• Wikidata: Q82466504
• Mol file: 13038-22-7.mol

Synonyms:8-Nonenyl Acetate;13038-22-7;ACETIC ACID 8-NONEN-1-YL ESTER;non-8-enyl acetate;ACETICACID8-NONEN-1-YLESTER;8-Nonen-1-ol, 1-acetate;non-8-en-1-yl acetate;Acetic Acid 8-Nonenyl Ester;9-Acetoxy-1-nonene;8-Nonen-1-yl acetate;SCHEMBL2839048;HUXQMCFHKGATCP-UHFFFAOYSA-;DTXSID10576680;MFCD00671492;AKOS025294280;CS-0361164;D88431;InChI=1/C11H20O2/c1-3-4-5-6-7-8-9-10-13-11(2)12/h3H,1,4-10H2,2H3

Chemical Property of 8-Nonenyl Acetate

Chemical Property:

• Refractive Index: 1.436
• Boiling Point: 155 °C / 24mmHg
• Density: 0.88
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 9
• Exact Mass: 184.146329876
• Heavy Atom Count: 13
• Complexity: 141

Purity/Quality:

99.9% ^*data from raw suppliers

8-Nonenyl Acetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OCCCCCCCC=C

Technology Process of 8-Nonenyl Acetate

There total 16 articles about 8-Nonenyl 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: 100.0%

non-8-en-1-ol (13038-21-6) + acetic anhydride (108-24-7) → non-8-en-1-yl acetate (13038-22-7)

Guidance literature:

With pyridine; at 20 ℃; for 72h;

DOI:10.1016/j.tet.2009.02.064

Reference yield: 81.0%

9-bromononyl acetate (53596-82-0) → non-8-en-1-yl acetate (13038-22-7)

Guidance literature:

With lithium carbonate; lithium bromide; In N,N-dimethyl-formamide; at 120 ℃; for 6h;

DOI:10.1007/s10600-006-0263-7

Reference yield: 77.0%

C20H36O4 → non-8-en-1-yl acetate (13038-22-7) + C20H36O4 (1160105-93-0)

Guidance literature:

With [Ru(pivalate)(CHC₆H₄OiPr)(C₁₀H₁₄C₃H₄N₂Mes)]; In tetrahydrofuran; at 35 ℃; for 4h; under 3800.26 Torr; Sealed tube;

DOI:10.1021/ja4010267

upstream raw materials:

1,9-nonanediol diacetate

non-8-en-1-ol

acetyl chloride

9-bromononyl acetate

Downstream raw materials:

(3S,6S)-3,6-dimethyloctane

8-methyl-2-decene

C₁₈H₃₆

(S,E)-14-methyl-8-hexadecenyl acetate

Refernces

Z -selective ethenolysis with a ruthenium metathesis catalyst: Experiment and theory

10.1021/ja4010267

The research involves several key chemicals that play crucial roles in the investigation of Z-selective ethenolysis and cross metathesis reactions. Methyl Oleate (6) is a standard substrate used to compare the ethenolysis reactivity and selectivity of metathesis catalysts. It is a fatty acid ester commonly used in olefin metathesis studies. 5-Decene (11) is an internal olefin used in cross metathesis reactions. The study investigates the reactivity of catalysts 3 and 5 with both cis- and trans-isomers of 5-decene. 8-Nonenyl Acetate (14) is another internal olefin substrate used in cross metathesis reactions. It is used in combination with 5-decene to study the formation of cross products.

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