Testololactone

Base Information

Chemical Name:Testololactone
CAS No.:4416-57-3
Molecular Formula:C19H26 O3
Molecular Weight:302.414
Hs Code.:
UNII:3RQL9VE1NB
Nikkaji Number:J39.509I
Wikidata:Q27102810
Metabolomics Workbench ID:35342
Mol file:4416-57-3.mol

Synonyms:hydrotestolactone;testololactone

Suppliers and Price of Testololactone

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
Testololactone
10mg
$ 1455.00

Medical Isotopes, Inc.
Testololactone
1 mg
$ 650.00

American Custom Chemicals Corporation
TESTOLOLACTONE 95.00%
5MG
$ 502.83

Total 4 raw suppliers

Chemical Property of Testololactone

Chemical Property:

Vapor Pressure:2.62E-09mmHg at 25°C
Melting Point:207-209 °C
Boiling Point:478.2°Cat760mmHg
Flash Point:211.2°C
PSA：43.37000
Density:1.15g/cm³
LogP:3.81390
Storage Temp.:Refrigerator
Solubility.:Chloroform (Slightly), DMSO (Slightly)
XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:302.18819469
Heavy Atom Count:22
Complexity:563

Purity/Quality:

99% ^*data from raw suppliers

Testololactone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC12CCC(=O)C=C1CCC3C2CCC4(C3CCC(=O)O4)C
Isomeric SMILES:C[C@]12CCC(=O)C=C1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CCC(=O)O4)C
Uses Testololactone, is the derivative of Testolactone (T154800), which is an antineoplastic agent that is a derivative of progesterone and is used to treat advanced stage breast cancer.

Technology Process of Testololactone

There total 7 articles about Testololactone 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: 60.9%

: 57-83-0
Progesterone

: 63-05-8
Androstenedione

: 4416-57-3
testololactone

Guidance literature:: With penicillium citreo-viride A_.C_.C_.C_. 0402; In acetone; at 27.5 ℃; for 120h; Microbiological reaction;
DOI:10.1016/j.steroids.2006.06.005

Reference yield: 52.6%

: 57-83-0
Progesterone

: 58-22-0
testosterone

: 63-05-8
Androstenedione

: 897-06-3
Androsta-1,4-diene-3,17-dione

: 4416-57-3
testololactone

Guidance literature:: With Fusarium dimerum; In water; at 30 ℃; for 36h; pH=7; Further Variations:; Reagents; pH-values; var. times; Product distribution;

Reference yield: 45.2%

: 521-17-5,1963-03-7,4593-57-1,4593-58-2,14504-94-0,16895-59-3,47122-33-8,64162-67-0,75767-22-5,139973-51-6,151284-19-4
5-androstenediol

: 63-05-8
Androstenedione

: 4416-57-3
testololactone

Guidance literature:: With penicillium citreo-viride A_.C_.C_.C_. 0402; In acetone; at 27.5 ℃; for 120h; Microbiological reaction;
DOI:10.1016/j.steroids.2006.06.005