Allyl laurate

Base Information

• Chemical Name: Allyl laurate
• CAS No.: 7003-75-0
• Molecular Formula: C15H28 O2
• Molecular Weight: 240.386
• Hs Code.: 2915900090
• NSC Number: 20977
• UNII: NJF9MS33KY
• DSSTox Substance ID: DTXSID90220316
• Nikkaji Number: J792.570K
• Wikidata: Q83097497
• ChEMBL ID: CHEMBL2229588
• Mol file: 7003-75-0.mol

Synonyms:ALLYL LAURATE;7003-75-0;prop-2-enyl dodecanoate;Dodecanoic acid, 2-propenyl ester;ALLYL DODECANOATE;AI3-02318;NSC 20977;NSC-20977;Dodecanoic acid, 2-propen-1-yl ester;Allyllaurate;Lauric acid allyl ester;NJF9MS33KY;2-Propen-1-yl dodecanoate;SCHEMBL248452;CHEMBL2229588;DTXSID90220316;NSC20977;MFCD00048428;FT-0622028;ALLYL LAURATE, (ALLYL DODECANOATE;LAURIC ACID ALLYL ESTER)

Chemical Property of Allyl laurate

Chemical Property:

• Vapor Pressure: 0.000737mmHg at 25°C
• Boiling Point: 135-136°C 4,5mm
• Flash Point: 130.8°C
• PSA: 26.30000
• Density: 0.875g/cm³
• LogP: 4.63650
• XLogP3: 5.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 13
• Exact Mass: 240.208930132
• Heavy Atom Count: 17
• Complexity: 187

Purity/Quality:

99% ^*data from raw suppliers

ALLYL LAURATE 98.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCC(=O)OCC=C

Technology Process of Allyl laurate

There total 7 articles about Allyl laurate 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: 89.0%

2-chloro-1-(chloromethyl)ethyl dodecanoate (7208-96-0) + butanone (78-93-3) → allyl dodecanoate (7003-75-0)

Guidance literature:

With sodium iodide; at 115 ℃; for 48h;

DOI:10.1021/jf900097j

Reference yield: 73.0%

lauric acid (143-07-7) + allyl alcohol (107-18-6) → allyl dodecanoate (7003-75-0)

Guidance literature:

With ethenetetracarbonitrile; for 48h; Ambient temperature;

DOI:10.1246/cl.1997.55

Reference yield: 57.0%

methyl n-dodecanoate (111-82-0) + allyl alcohol (107-18-6) → allyl dodecanoate (7003-75-0)

Guidance literature:

With tetracyanomethylene; at 60 ℃; for 48h;

DOI:10.1246/cl.1997.55

upstream raw materials:

lauric acid

allyl alcohol

n-dodecanoyl chloride

methyl n-dodecanoate

Downstream raw materials:

lauric acid

allyl acrylate

butyl laurate

ethyl laurate

Refernces

• 1、 Escriba, Marc,Barbut, Montserrat,Eras, Jordi,Canela, Ramon,Avilla, Jesus,Balcells, Merge. "Synthesis of allyl esters of fatty acids and their ovicidal effect on Cydia pomonella (L.)". experimental part. p. 4849 - 4853. Retrieved 2010/06/14.
• 2、 Gangadhar, A.,Subbarao, R.,Lakshminarayana, G.. "A FACILE SYNTHESIS OF 1(3)-ACYLGLYCEROLS". . p. 2505 - 2514. Retrieved 2007/10/02.