Yakkasterone

Base Information

Chemical Name:Yakkasterone
CAS No.:13027-33-3
Molecular Formula:C₂₇H₄₆O₃
Molecular Weight:418.66
Hs Code.:
UNII:YO7G6S09N3
DSSTox Substance ID:DTXSID80926658
Nikkaji Number:J143.767D
Wikidata:Q27896404
Metabolomics Workbench ID:34428
ChEMBL ID:CHEMBL1277915
Mol file:13027-33-3.mol

Synonyms:3beta, 5alpha-dihydroxycholestan-6-one;yakkasterone;YS 64;YS-64

Suppliers and Price of Yakkasterone

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

TRC
5α-hydroxy-6-ketoCholesterol
2.5mg
$ 90.00

TRC
5α-hydroxy-6-ketoCholesterol
1mg
$ 45.00

Cayman Chemical
5α-hydroxy-6-keto Cholesterol ≥98%
1mg
$ 25.00

Cayman Chemical
5α-hydroxy-6-keto Cholesterol ≥98%
10mg
$ 225.00

Cayman Chemical
5α-hydroxy-6-keto Cholesterol ≥98%
5mg
$ 119.00

AK Scientific
5alpha-Cholestan-3beta,5alpha-diol-6-one
10mg
$ 403.00

AK Scientific
5alpha-Cholestan-3beta,5alpha-diol-6-one
1mg
$ 133.00

Total 7 raw suppliers

Chemical Property of Yakkasterone

Chemical Property:

Vapor Pressure:2.15E-13mmHg at 25°C
Boiling Point:528.9°Cat760mmHg
Flash Point:287.7°C
PSA：57.53000
Density:1.061g/cm³
LogP:5.76250
XLogP3:7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:418.34469533
Heavy Atom Count:30
Complexity:659

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

5α-hydroxy-6-ketoCholesterol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CCCC(C)C1CCC2C1(CCC3C2CC(=O)C4(C3(CCC(C4)O)C)O)C
Isomeric SMILES:C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC(=O)[C@@]4([C@@]3(CC[C@@H](C4)O)C)O)C

Technology Process of Yakkasterone

There total 41 articles about Yakkasterone 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: 95.0%

: 1253-84-5
cholestanetriol

: 2953-37-9,6580-08-1,16526-63-9,97100-50-0,115792-36-4,13027-33-3
3β,5-dihydroxy-5α-cholestan-6-one

Guidance literature:: With N-Bromosuccinimide; In 1,4-dioxane; water;

Reference yield: 85.0%

: 1253-84-5
cholestanetriol

: 2953-37-9,6580-08-1,16526-63-9,97100-50-0,115792-36-4,13027-33-3
3β,5-dihydroxy-5α-cholestan-6-one

: 20281-70-3
5α-cholestane-5-ol-3,6-dione

Guidance literature:: With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In dimethyl sulfoxide; for 0.75h; Ambient temperature;
DOI:10.1016/0040-4039(94)80038-3