Androsta-3,5-diene-7,17-dione

Base Information

Chemical Name:Androsta-3,5-diene-7,17-dione
CAS No.:1420-49-1
Molecular Formula:C19H24O2
Molecular Weight:284.398
Hs Code.:
NSC Number:134910
DSSTox Substance ID:DTXSID50931294
Pharos Ligand ID:AAAQVT6WNKFP
ChEMBL ID:CHEMBL262723
Mol file:1420-49-1.mol

Synonyms:NSC 134910;

Suppliers and Price of Androsta-3,5-diene-7,17-dione

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
Arimistane
1g
$ 50.00

TRC
Arimistane
5g
$ 105.00

Chemenu
Androst-3,5-diene-7,17-dione 98%
100g
$ 350.00

Cayman Chemical
Androst-3,5-diene-7,17-dione ≥98%
10mg
$ 63.00

Cayman Chemical
Androst-3,5-diene-7,17-dione ≥98%
5mg
$ 35.00

Total 84 raw suppliers

Chemical Property of Androsta-3,5-diene-7,17-dione

Chemical Property:

Vapor Pressure:2.88E-08mmHg at 25°C
Melting Point:167-168℃
Refractive Index:1.568
Boiling Point:449.3 °C at 760 mmHg
Flash Point:167.5 °C
PSA：34.14000
Density:1.14g/cm³
LogP:3.86340
Storage Temp.:-20°C Freezer
Solubility.:Chloroform (Sparingly), Methanol (Slightly)
XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:284.177630004
Heavy Atom Count:21
Complexity:584

Purity/Quality:

99%, ^*data from raw suppliers

Arimistane ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC12CCC3C(C1CCC2=O)C(=O)C=C4C3(CCC=C4)C
Uses Arimistane is an aromatase inhibitor used in the reduction of estrogen production as well as a potential reagent in the synthesis of anti-cancer agent MGC-803.

Technology Process of Androsta-3,5-diene-7,17-dione

There total 13 articles about Androsta-3,5-diene-7,17-dione 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%