(5alpha)-17-(3-Pyridinyl)androst-16-en-3-one

Base Information

Chemical Name:(5alpha)-17-(3-Pyridinyl)androst-16-en-3-one
CAS No.:154229-26-2
Molecular Formula:C₂₄H₃₁NO
Molecular Weight:349.516
Hs Code.:
UNII:675L8BAG4G
DSSTox Substance ID:DTXSID00471175
Nikkaji Number:J686.896G
Wikidata:Q30647374
Wikipedia:3-Keto-5%CE%B1-abiraterone
Mol file:154229-26-2.mol

Synonyms:3-keto-5alpha-abiraterone;3-ketoabiraterone

Suppliers and Price of (5alpha)-17-(3-Pyridinyl)androst-16-en-3-one

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)-17-(3-Pyridinyl)androst-16-en-3-one
50mg
$ 1320.00

Total 13 raw suppliers

Chemical Property of (5alpha)-17-(3-Pyridinyl)androst-16-en-3-one

Chemical Property:

Boiling Point:486.0±45.0 °C(Predicted)
PKA:5.32±0.12(Predicted)
PSA：29.96000
Density:1.094±0.06 g/cm3(Predicted)
LogP:5.68670
XLogP3:5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:349.240564612
Heavy Atom Count:26
Complexity:624

Purity/Quality:

99% ^*data from raw suppliers

(5α)-17-(3-Pyridinyl)androst-16-en-3-one ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC12CCC(=O)CC1CCC3C2CCC4(C3CC=C4C5=CN=CC=C5)C
Isomeric SMILES:C[C@]12CCC(=O)C[C@@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC=C4C5=CN=CC=C5)C
Uses (5α)-17-(3-Pyridinyl)androst-16-en-3-one is a related compound of Abiraterone (A108490). (5α)-17-(3-Pyridinyl)androst-16-en-3-one is a 17-(3-pyridyl)-substituted steroid useful in cancer treatment such as prostatic cancer and breast cancer.

Technology Process of (5alpha)-17-(3-Pyridinyl)androst-16-en-3-one

There total 22 articles about (5alpha)-17-(3-Pyridinyl)androst-16-en-3-one 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: 86.0%