Halopredone acetate

Base Information Edit

Chemical Name:Halopredone acetate
CAS No.:57781-14-3
Molecular Formula:C25H29 Br F2 O7
Molecular Weight:559.402
Hs Code.:
European Community (EC) Number:260-951-4
UNII:24NUL39JY1
DSSTox Substance ID:DTXSID30206477
Nikkaji Number:J11.144I
Wikidata:Q27253865
NCI Thesaurus Code:C166537
Pharos Ligand ID:58FGR8XTCDLS
ChEMBL ID:CHEMBL2106520
Mol file:57781-14-3.mol

Synonyms:halopredone acetate;halopredone acetate, (6alpha,11beta)-isomer;THS 201;THS-201;Topicon

Suppliers and Price of Halopredone acetate

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

American Custom Chemicals Corporation
2-BROMO-6BETA,9-DIFLUORO-11BETA,17,21-TRIHYDROXYPREGNA-1,4-DIENE-3,20-DIONE 17,21-DI(ACETATE) 95.00%
5MG
$ 505.75

Total 3 raw suppliers

Chemical Property of Halopredone acetate Edit

Chemical Property:

Vapor Pressure:5.36E-18mmHg at 25°C
Melting Point:290-292° (dec)
Refractive Index:1.3760 (estimate)
Boiling Point:620.5°C at 760 mmHg
Flash Point:329.1°C
PSA：106.97000
Density:1.49g/cm³
LogP:3.46190
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:6
Exact Mass:558.10647
Heavy Atom Count:35
Complexity:1070

Purity/Quality:

99% ^*data from raw suppliers

2-BROMO-6BETA,9-DIFLUORO-11BETA,17,21-TRIHYDROXYPREGNA-1,4-DIENE-3,20-DIONE 17,21-DI(ACETATE) 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OCC(=O)C1(CCC2C1(CC(C3(C2CC(C4=CC(=O)C(=CC43C)Br)F)F)O)C)OC(=O)C
Isomeric SMILES:CC(=O)OCC(=O)[C@]1(CC[C@@H]2[C@@]1(C[C@@H]([C@]3([C@H]2C[C@H](C4=CC(=O)C(=C[C@@]43C)Br)F)F)O)C)OC(=O)C
Uses Anti-inflammatory (topical).

Technology Process of Halopredone acetate

There total 4 articles about Halopredone acetate 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: