Viprostol

Base Information

Chemical Name:Viprostol
CAS No.:73621-92-8
Deprecated CAS:93522-21-5
Molecular Formula:C₂₃H₃₆O₅
Molecular Weight:392.536
Hs Code.:
UNII:O2Y6I4Y8TF
DSSTox Substance ID:DTXSID301021620
Nikkaji Number:J3.043.122G
Wikidata:Q27285247
NCI Thesaurus Code:C152893
ChEMBL ID:CHEMBL2107669
Mol file:73621-92-8.mol

Synonyms:15-(deoxy)-16-hydroxy-16-vinylprostaglandin E2 methyl ester;15-deoxy-16-hydroxy-16-vinyl-PGE2 methyl ester;CL 115,347;CL 115347;DHV-PGE2Me;viprostol;viprostol, (+-)-isomer

Suppliers and Price of Viprostol

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

Total 1 raw suppliers

Chemical Property of Viprostol

Chemical Property:

PSA：83.83000
LogP:3.89570
XLogP3:3.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:14
Exact Mass:392.25627424
Heavy Atom Count:28
Complexity:565

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC(CC=CC1C(CC(=O)C1CC=CCCCC(=O)OC)O)(C=C)O
Isomeric SMILES:CCCCC(C/C=C/[C@H]1[C@@H](CC(=O)[C@@H]1C/C=C\CCCC(=O)OC)O)(C=C)O

Technology Process of Viprostol

There total 5 articles about Viprostol 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:

: 2918-13-0
1-hepten-3-one

: 73621-92-8,73647-73-1,81445-69-4,81445-71-8,90457-41-3,104012-13-7,115810-19-0
(16RS)-(+/-)-15-deoxy-16-hydroxy-16-vinyl-PGE2 methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 33 percent

2: 90 percent / imidazole / dimethylformamide

With 1H-imidazole; In N,N-dimethyl-formamide;
DOI:10.1021/jm00347a003

Reference yield:

: 4938-52-7
1-hepten-3-ol

: 73621-92-8,73647-73-1,81445-69-4,81445-71-8,90457-41-3,104012-13-7,115810-19-0
(16RS)-(+/-)-15-deoxy-16-hydroxy-16-vinyl-PGE2 methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 41 percent / pyridinium chlorochromate

2: 33 percent

3: 90 percent / imidazole / dimethylformamide

With 1H-imidazole; pyridinium chlorochromate; In N,N-dimethyl-formamide;
DOI:10.1021/jm00347a003

Reference yield:

: 81416-65-1
(+/-)-4-hydroxy-4-vinyl-1-octyne

: 73621-92-8,73647-73-1,81445-69-4,81445-71-8,90457-41-3,104012-13-7,115810-19-0
(16RS)-(+/-)-15-deoxy-16-hydroxy-16-vinyl-PGE2 methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / imidazole / dimethylformamide

With 1H-imidazole; In N,N-dimethyl-formamide;
DOI:10.1021/jm00347a003