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3a,7a-Dihydroxy-5a-cholanate

Base Information
  • Chemical Name:3a,7a-Dihydroxy-5a-cholanate
  • CAS No.:15357-34-3
  • Molecular Formula:C24H40 O4
  • Molecular Weight:392.579
  • Hs Code.:
  • Mol file:15357-34-3.mol
3a,7a-Dihydroxy-5a-cholanate

Synonyms:3a,7a-Dihydroxy-5a-cholanate;3a,7a-Dihydroxy-5a-cholanic acid;3a,7a-dihydroxy-(5a)-cholan-24-oate;3a,7a-dihydroxy-(5a)-cholan-24-oic acid

Suppliers and Price of 3a,7a-Dihydroxy-5a-cholanate
Supply Marketing:
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
Total 22 raw suppliers
Chemical Property of 3a,7a-Dihydroxy-5a-cholanate
Chemical Property:
  • Vapor Pressure:2.98E-14mmHg at 25°C 
  • Boiling Point:547.1°Cat760mmHg 
  • Flash Point:298.8°C 
  • PSA:77.76000 
  • Density:1.128g/cm3 
  • LogP:4.47790 
  • XLogP3:4.9
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:392.29265975
  • Heavy Atom Count:28
  • Complexity:605
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CCC(=O)O)C1CCC2C1(CCC3C2C(CC4C3(CCC(C4)O)C)O)C
  • Isomeric SMILES:C[C@H](CCC(=O)O)C1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2[C@@H](C[C@@H]4[C@@]3(CC[C@H](C4)O)C)O)C
Technology Process of 3a,7a-Dihydroxy-5a-cholanate

There total 16 articles about 3a,7a-Dihydroxy-5a-cholanate 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:
Multi-step reaction with 5 steps
1.1: phosphorus pentoxide / chloroform / 4 h / 20 °C / Inert atmosphere
2.1: 2-iodoxybenzoic acid / dimethyl sulfoxide / 72 h / 40 °C / Inert atmosphere
3.1: ammonia; lithium; tert-butyl alcohol / tetrahydrofuran / 0.08 h / -78 °C / Inert atmosphere
4.1: potassium tri-sec-butyl-borohydride / tetrahydrofuran / 2 h / -78 °C / Inert atmosphere
5.1: hydrogenchloride / methanol / 2 h / Reflux; Inert atmosphere
5.2: 8 h / Reflux; Inert atmosphere
With hydrogenchloride; 2-iodoxybenzoic acid; phosphorus pentoxide; ammonia; lithium; potassium tri-sec-butyl-borohydride; tert-butyl alcohol; In tetrahydrofuran; methanol; chloroform; dimethyl sulfoxide; 3.1: Birch reduction;
DOI:10.1016/j.tetlet.2011.05.140
Guidance literature:
aus 5-en-Cholinsaeure durch Bioreaktion in 'Carp bile';
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