16,16-dimethyl-PGE1

Base Information

• Chemical Name: 16,16-dimethyl-PGE1
• CAS No.: 41692-15-3
• Molecular Formula: C₂₂H₃₈O₅
• Molecular Weight: 382.541
• Wikidata: Q76286286
• Metabolomics Workbench ID: 2418
• Mol file: 41692-15-3.mol

Synonyms:16,16-dimethylprostaglandin E;16,16-dimethylprostaglandin E, (11alpha,13E,15S)-isomer

Chemical Property of 16,16-dimethyl-PGE1

Chemical Property:

• Vapor Pressure: 5.9E-14mmHg at 25°C
• Boiling Point: 540.9°Cat760mmHg
• Flash Point: 295°C
• PSA: 94.83000
• Density: 1.104g/cm³
• LogP: 4.11120
• XLogP3: 4
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 13
• Exact Mass: 382.27192431
• Heavy Atom Count: 27
• Complexity: 497

Purity/Quality:

98% ^*data from raw suppliers

16,16-dimethyl Prostaglandin E1 ≥98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCC(C)(C)C(C=CC1C(CC(=O)C1CCCCCCC(=O)O)O)O
• Isomeric SMILES: CCCCC(C)(C)[C@@H](/C=C/[C@H]1[C@@H](CC(=O)[C@@H]1CCCCCCC(=O)O)O)O

Technology Process of 16,16-dimethyl-PGE1

There total 1 articles about 16,16-dimethyl-PGE1 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:

7-[(1R,2R,3R,5S)-2-[(E)-(R)-4,4-Dimethyl-3-(tetrahydro-pyran-2-yloxy)-oct-1-enyl]-5-hydroxy-3-(tetrahydro-pyran-2-yloxy)-cyclopentyl]-heptanoic acid → 16,16-Dimethylprostaglandin E1 (41692-15-3)

Guidance literature:

Multistep reaction; (i) CrO₃, aq. MnSO₄, H₂SO₄, (ii) AcOH, THF;

Reference yield:

16,16-Dimethylprostaglandin E1 (41692-15-3) → 16.16-Dimethyl-PGA1 (41692-24-4)

Guidance literature:

With acetic acid;

Reference yield:

16,16-Dimethylprostaglandin E1 (41692-15-3) + 4-chloro-phenol (106-48-9,82344-39-6) → 16,16-Dimethyl-PGE(1)-p-chlorphenylester (41661-72-7)

Guidance literature:

Multistep reaction; (i) DCC, CHCl₃, (ii) /BRN= 507004/, Py;

Downstream raw materials:

16.16-Dimethyl-PGA1

16,16-Dimethyl-PGE⁽¹⁾-p-chlorphenylester

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