Tetracosyl tetracosanoate

Base Information

• Chemical Name: Tetracosyl tetracosanoate
• CAS No.: 1001-43-0
• Molecular Formula: C48H96 O2
• Molecular Weight: 705.289
• UNII: OI4628R01I
• DSSTox Substance ID: DTXSID20142936
• Nikkaji Number: J370.104B
• Wikidata: Q27285659
• Mol file: 1001-43-0.mol

Synonyms:Tetracosyl tetracosanoate;Tetracosanoic acid, tetracosyl ester;1-Tetracosanyl tetracosanoate;UNII-OI4628R01I;Lignoceryl Lignocerate;OI4628R01I;1001-43-0;tetracosanyl tetracosanoate;SCHEMBL11041639;tetracosyl estertetracosanoic acid;DTXSID20142936;1-TETRACOSYL TETRACOSANOATE;Tetracosanoic acid tetracosyl ester;C48H96O2;Q27285659

Chemical Property of Tetracosyl tetracosanoate

Chemical Property:

• Vapor Pressure: 1.79E-17mmHg at 25°C
• Boiling Point: 663.5°C at 760 mmHg
• Flash Point: 370.8°C
• Density: 0.855g/cm³
• XLogP3: 23.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 46
• Exact Mass: 704.74103230
• Heavy Atom Count: 50
• Complexity: 601

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCCCCCCCC

Technology Process of Tetracosyl tetracosanoate

There total 3 articles about Tetracosyl tetracosanoate 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:

tetracosyl alcohol (506-51-4) → tetracosanoic acid tetracosyl ester (1001-43-0)

Guidance literature:

With quinoline; chloroform;

Reference yield:

tetracosanoic acid phenyl ester (460335-09-5) → tetracosanoic acid tetracosyl ester (1001-43-0)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium; alcohol

2: chloroform; quinoline

With quinoline; ethanol; chloroform; sodium;

Reference yield:

→ tetracosanoic acid tetracosyl ester (1001-43-0)

Guidance literature:

DOI:10.1016/0009-3084(71)90063-6

upstream raw materials:

tetracosyl alcohol

tetracosanoic acid phenyl ester

Downstream raw materials:

tetracosyl alcohol

tetracosyl acetate