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3,7-Dihydroxycoprostanic acid

Base Information Edit
  • Chemical Name:3,7-Dihydroxycoprostanic acid
  • CAS No.:17974-66-2
  • Molecular Formula:C27H46 O4
  • Molecular Weight:434.66
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70939252
  • Mol file:17974-66-2.mol
3,7-Dihydroxycoprostanic acid

Synonyms:3 alpha,7 alpha-dihydroxy-5 beta-cholestan-26-oic acid;3,7-DHCA;3,7-dihydroxycholestan-26-oic acid

Suppliers and Price of 3,7-Dihydroxycoprostanic acid
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
  • Medical Isotopes, Inc.
  • 3α,7α-DihydroxycoprostanicAcid
  • 1 mg
  • $ 290.00
  • ChemScene
  • 3α,7α-Dihydroxycoprostanicacid
  • 10mg
  • $ 850.00
  • ChemScene
  • 3α,7α-Dihydroxycoprostanicacid
  • 5mg
  • $ 500.00
Total 3 raw suppliers
Chemical Property of 3,7-Dihydroxycoprostanic acid Edit
Chemical Property:
  • Vapor Pressure:1.42E-15mmHg at 25°C 
  • Refractive Index:1.533 
  • Boiling Point:574.2°Cat760mmHg 
  • Flash Point:315.1°C 
  • PSA:77.76000 
  • Density:1.092g/cm3 
  • LogP:5.50410 
  • XLogP3:6.6
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:6
  • Exact Mass:434.33960994
  • Heavy Atom Count:31
  • Complexity:664
Purity/Quality:

99%min *data from raw suppliers

3α,7α-DihydroxycoprostanicAcid *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CCCC(C)C(=O)O)C1CCC2C1(CCC3C2C(CC4C3(CCC(C4)O)C)O)C
  • Isomeric SMILES:C[C@H](CCCC(C)C(=O)O)C1CCC2[C@@]1(CCC3C2[C@@H](C[C@H]4[C@@]3(CC[C@H](C4)O)C)O)C
Technology Process of 3,7-Dihydroxycoprostanic acid

There total 11 articles about 3,7-Dihydroxycoprostanic acid 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 lithium chloride; In dimethyl sulfoxide; at 160 ℃; for 1h;
DOI:10.1016/S0039-128X(99)00099-9
Guidance literature:
Multi-step reaction with 5 steps
1: 77 percent / BH3*THF / tetrahydrofuran / 20 h / 20 °C
2: 94 percent / I2; Ph3P; imidazole / tetrahydrofuran / 4 h / 20 °C
3: 75 percent / NaH / tetrahydrofuran; dimethylsulfoxide / 3 h / 20 °C
4: 95 percent / KOH / ethanol / 3 h / Heating
5: 61 percent / aq. LiCl / dimethylsulfoxide / 1 h / 160 °C
With 1H-imidazole; potassium hydroxide; borane-THF; iodine; sodium hydride; triphenylphosphine; lithium chloride; In tetrahydrofuran; ethanol; dimethyl sulfoxide; 1: Reduction / 2: Iodination / 3: Substitution / 4: Deformylation; Hydrolysis / 5: Decarboxylation;
DOI:10.1016/S0039-128X(99)00099-9
Guidance literature:
Multi-step reaction with 4 steps
1: 94 percent / I2; Ph3P; imidazole / tetrahydrofuran / 4 h / 20 °C
2: 75 percent / NaH / tetrahydrofuran; dimethylsulfoxide / 3 h / 20 °C
3: 95 percent / KOH / ethanol / 3 h / Heating
4: 61 percent / aq. LiCl / dimethylsulfoxide / 1 h / 160 °C
With 1H-imidazole; potassium hydroxide; iodine; sodium hydride; triphenylphosphine; lithium chloride; In tetrahydrofuran; ethanol; dimethyl sulfoxide; 1: Iodination / 2: Substitution / 3: Deformylation; Hydrolysis / 4: Decarboxylation;
DOI:10.1016/S0039-128X(99)00099-9
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