16-phenyl tetranor Prostaglandin E2

Base Information

• Chemical Name: 16-phenyl tetranor Prostaglandin E2
• CAS No.: 38315-44-5
• Molecular Formula: C22H28O5
• Molecular Weight: 372.45
• Wikidata: Q76286296
• Metabolomics Workbench ID: 2427
• Mol file: 38315-44-5.mol

Synonyms:16-phenyl tetranor Prostaglandin E2;38315-44-5;16-phenyl-tetranor-PGE2;(Z)-7-[(1R,2R,3R)-3-hydroxy-2-[(E,3S)-3-hydroxy-4-phenylbut-1-enyl]-5-oxocyclopentyl]hept-5-enoic acid;16-phenyl-tetranor-Prostaglandin E2;9-oxo-11R,15S-dihydroxy-16-phenyl-17,18,19,20-tetranor-5Z,13E-prostadienoic acid;LMFA03010066;CHEBI:165308;HMS3648J11;PD021124;SR-01000946437;SR-01000946437-1

Chemical Property of 16-phenyl tetranor Prostaglandin E2

Chemical Property:

• PSA: 94.83000
• LogP: 2.91350
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 10
• Exact Mass: 372.19367399
• Heavy Atom Count: 27
• Complexity: 533

Purity/Quality:

99% ，98% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(C(C(C1=O)CC=CCCCC(=O)O)C=CC(CC2=CC=CC=C2)O)O
• Isomeric SMILES: C1[C@H]([C@@H]([C@H](C1=O)C/C=C\CCCC(=O)O)/C=C/[C@H](CC2=CC=CC=C2)O)O

Technology Process of 16-phenyl tetranor Prostaglandin E2

There total 2 articles about 16-phenyl tetranor Prostaglandin E2 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:

→ (Z)-7-[(1R,2S,3R)-3-Hydroxy-2-((E)-3-hydroxy-4-phenyl-but-1-enyl)-5-oxo-cyclopentyl]-hept-5-enoic acid (38315-44-5,52390-11-1,54324-16-2,54324-17-3,57968-87-3,57968-88-4,59686-06-5)

Guidance literature:

entspr. Ether, saure Hydrolyse;

Reference yield:

→ 16-Phenyl-17,18,19,20-tetranor-PGE(2) (38315-44-5,52390-11-1,54324-16-2,54324-17-3,57968-87-3,57968-88-4,59686-06-5)

Guidance literature:

entspr. Aethylester (aus den opt. akt. Glykolen Bsp.9);