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Tetracosanoyl chloride

Base Information Edit
  • Chemical Name:Tetracosanoyl chloride
  • CAS No.:58576-73-1
  • Molecular Formula:C24H47ClO
  • Molecular Weight:387.09
  • Hs Code.:
  • DSSTox Substance ID:DTXSID801314494
  • Nikkaji Number:J355.064H
  • Mol file:58576-73-1.mol
Tetracosanoyl chloride

Synonyms:Tetracosanoyl chloride;58576-73-1;Tetracosanoic acid chloride;SCHEMBL3674715;DTXSID801314494

Suppliers and Price of Tetracosanoyl chloride
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • TetracosanoylChloride
  • 10mg
  • $ 230.00
Total 1 raw suppliers
Chemical Property of Tetracosanoyl chloride Edit
Chemical Property:
  • PSA:17.07000 
  • LogP:9.35390 
  • XLogP3:11.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:22
  • Exact Mass:386.3315438
  • Heavy Atom Count:26
  • Complexity:277
Purity/Quality:

99% *data from raw suppliers

TetracosanoylChloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCCCCCCCCCCCCCC(=O)Cl
  • Uses Tetracosanoyl Chloride is an intermediate in the synthesis of C24 Ceramide (C263450).
Technology Process of Tetracosanoyl chloride

There total 6 articles about Tetracosanoyl chloride 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:
Guidance literature:
With thionyl chloride;
Guidance literature:
Multi-step reaction with 4 steps
1: HCl / CHCl3 / 5 h / Heating
2: 86 percent / NaOH / ethanol / 1 h / Heating
3: 81.53 percent / powdered potassium hydroxide, hydrazine hydrate / ethane-1,2-diol / 1.) reflux, 1 h, 2.) reflux, 1 h
4: thionyl chloride, dimethylformamide
With hydrogenchloride; potassium hydroxide; sodium hydroxide; thionyl chloride; hydrazine hydrate; N,N-dimethyl-formamide; In ethanol; chloroform; ethylene glycol;
DOI:10.1016/S0040-4020(01)97739-7
Guidance literature:
Multi-step reaction with 2 steps
1: 81.53 percent / powdered potassium hydroxide, hydrazine hydrate / ethane-1,2-diol / 1.) reflux, 1 h, 2.) reflux, 1 h
2: thionyl chloride, dimethylformamide
With potassium hydroxide; thionyl chloride; hydrazine hydrate; N,N-dimethyl-formamide; In ethylene glycol;
DOI:10.1016/S0040-4020(01)97739-7
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