alpha-Linolenic anhydride

Base Information

• Chemical Name: alpha-Linolenic anhydride
• CAS No.: 55726-27-7
• Molecular Formula: C36H58O3
• Molecular Weight: 538.855
• European Community (EC) Number: 633-496-8
• Mol file: 55726-27-7.mol

Synonyms:55726-27-7;ALPHA-LINOLENIC ANHYDRIDE;SCHEMBL3283651

Chemical Property of alpha-Linolenic anhydride

Chemical Property:

• PSA: 43.37000
• LogP: 11.23520
• Storage Temp.: ?20°C
• XLogP3: 12.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 28
• Exact Mass: 538.43859571
• Heavy Atom Count: 39
• Complexity: 674

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC=CCC=CCC=CCCCCCCCC(=O)OC(=O)CCCCCCCC=CCC=CCC=CCC
• Isomeric SMILES: CC/C=C/C/C=C/C/C=C/CCCCCCCC(=O)OC(=O)CCCCCCC/C=C/C/C=C/C/C=C/CC

Technology Process of alpha-Linolenic anhydride

There total 1 articles about alpha-Linolenic anhydride 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:

(9Z,12Z,15Z)-octadeca-9-12,15-trienoic acid (463-40-1,1955-33-5,21661-10-9,21661-09-6,21661-13-2,21661-11-0) → α-linolenic acid anhydride (55726-27-7)

Guidance literature:

With dicyclohexyl-carbodiimide; In dichloromethane; at 20 ℃; for 4h;

DOI:10.1016/0024-3205(96)00101-4

Reference yield: 62.0%

α-linolenic acid anhydride (55726-27-7) + estrone-2,4,16,16-d4 (53866-34-5,350820-16-5) → 2,4,16,16-D4-estrone-3-linolenate

Guidance literature:

With dmap; In pyridine; at 50 ℃; for 0.0333333h; microwave irradiation;

DOI:10.1016/j.steroids.2005.08.001

Reference yield:

α-linolenic acid anhydride (55726-27-7) → 2,3-dihydroxypropyl (9Z,12Z,15Z)-9,12,15-octadecatrienoate (18465-99-1,56554-41-7,75685-85-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 69.5 percent / DMAP / benzene / 8 h / Ambient temperature

2: 43 percent / TFA / CH₂Cl₂ / 12 h / 0 °C

With dmap; trifluoroacetic acid; In dichloromethane; benzene;

DOI:10.1021/jm00379a019

upstream raw materials:

(9Z,12Z,15Z)-octadeca-9-12,15-trienoic acid

Downstream raw materials:

N-Linolenoyldopamine

2,3-dihydroxypropyl (9Z,12Z,15Z)-9,12,15-octadecatrienoate

1-linolenoyl-2,3-bis(4-aminobutyryl)propane-1,2,3-triol

1,2-dilinolenoyl-3-(4-aminobutyryl)propane-1,2,3-triol