Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

10-Methylthioethyl estra-4,9(11)-diene 3,17-dione

Base Information Edit
  • Chemical Name:10-Methylthioethyl estra-4,9(11)-diene 3,17-dione
  • CAS No.:137437-16-2
  • Molecular Formula:C21H28O2S
  • Molecular Weight:344.518
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90160182
  • Nikkaji Number:J729.824B
  • Wikidata:Q83028546
  • Pharos Ligand ID:KFLBFDRVZ1W2
  • ChEMBL ID:CHEMBL3752510
  • Mol file:137437-16-2.mol
10-Methylthioethyl estra-4,9(11)-diene 3,17-dione

Synonyms:10-methylthioethyl estra-4,9(11)-diene 3,17-dione;RU 54115;RU-54115;RU54115

Suppliers and Price of 10-Methylthioethyl estra-4,9(11)-diene 3,17-dione
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
Total 1 raw suppliers
Chemical Property of 10-Methylthioethyl estra-4,9(11)-diene 3,17-dione Edit
Chemical Property:
  • Vapor Pressure:8.14E-11mmHg at 25°C 
  • Boiling Point:517.5°Cat760mmHg 
  • Flash Point:217.8°C 
  • PSA:59.44000 
  • Density:1.16g/cm3 
  • LogP:4.74070 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:344.18100131
  • Heavy Atom Count:24
  • Complexity:646
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12CC=C3C(C1CCC2=O)CCC4=CC(=O)CCC43CCSC
  • Isomeric SMILES:C[C@]12CC=C3[C@H]([C@@H]1CCC2=O)CCC4=CC(=O)CC[C@@]43CCSC
Technology Process of 10-Methylthioethyl estra-4,9(11)-diene 3,17-dione

There total 5 articles about 10-Methylthioethyl estra-4,9(11)-diene 3,17-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:
Guidance literature:
With hydrogenchloride; In ethanol; for 1h; Yield given; Heating;
DOI:10.1021/jm950539l
Guidance literature:
Multi-step reaction with 5 steps
1: 71.6 percent / 1,2-dichloro-ethane / 8 h / Heating
2: 85.5 percent / lithium aluminum hydride / tetrahydrofuran / 1.) -50 deg C, 30 min, 2.) RT, 2 h
3: 100 percent / triethylamine / CH2Cl2 / 0.75 h / 0 °C
4: dimethylformamide / 1 h / 35 °C
5: 6 N hydrochloric acid / ethanol / 1 h / Heating
With hydrogenchloride; lithium aluminium tetrahydride; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1021/jm950539l
Guidance literature:
Multi-step reaction with 3 steps
1: 100 percent / triethylamine / CH2Cl2 / 0.75 h / 0 °C
2: dimethylformamide / 1 h / 35 °C
3: 6 N hydrochloric acid / ethanol / 1 h / Heating
With hydrogenchloride; triethylamine; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm950539l
Post RFQ for Price