10-Undecenoic acid octyl ester

Base Information

• Chemical Name: 10-Undecenoic acid octyl ester
• CAS No.: 28080-85-5
• Molecular Formula: C19H36O2
• Molecular Weight: 296.48800
• Hs Code.: 2916190090
• Mol file: 28080-85-5.mol

Synonyms:1-octyl 10-undecenoate;caprylyl undecylenate;undecylenic acid octyl ester;Octyl 10-undecenoate;10-Undecenoic acid,octyl ester;

Chemical Property of 10-Undecenoic acid octyl ester

Chemical Property:

• PSA: 26.30000
• LogP: 6.19690

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 10-Undecenoic acid octyl ester

There total 3 articles about 10-Undecenoic acid octyl ester 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: 98.0%

undec-10-enoyl chloride (38460-95-6) + octanol (111-87-5) → 1-octyl 10-undecenoate (28080-85-5)

Guidance literature:

With 1-methyl-1H-imidazole; N,N,N,N,-tetramethylethylenediamine; potassium carbonate; In acetonitrile; at 0 - 5 ℃; for 1h;

DOI:10.1016/j.tet.2007.08.117

Reference yield: 75.0%

octanol (111-87-5) + 10-undecenoic acid (112-38-9) → 1-octyl 10-undecenoate (28080-85-5)

Guidance literature:

With Rhizomucor miehei lipase; In aq. phosphate buffer; at 30 ℃; for 24h; Enzymatic reaction;

DOI:10.1039/d1sc05660c

Reference yield:

octanol (111-87-5) + Methyl 10-undecenoate (111-81-9) → 1-octyl 10-undecenoate (28080-85-5)

Guidance literature:

Novozym 435; at 60 ℃; for 6h; under 15.0015 Torr; Enzymatic reaction;

upstream raw materials:

undec-10-enoyl chloride

octanol

Methyl 10-undecenoate

10-undecenoic acid

Refernces

• 1、 Nakatsuji, Hidefumi,Morimoto, Mami,Misaki, Tomonori,Tanabe, Yoo. "Mild, powerful, and robust methods for esterification, amide formation, and thioesterification between acid chlorides and alcohols, amines, thiols, respectively". . p. 12071 - 12080. Retrieved 2008/03/13.