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Otosenine 12-acetate

Base Information
  • Chemical Name:Otosenine 12-acetate
  • CAS No.:16958-30-8
  • Molecular Formula:C21H29NO8
  • Molecular Weight:423.463
  • Hs Code.:
  • Wikidata:Q105241643
  • Mol file:16958-30-8.mol
Otosenine 12-acetate

Synonyms:Florosenine;Florosenine (neutral);Otosenine 12-acetate;[(1R,3'S,6R,7R,11Z)-3',6,7,14-tetramethyl-3,8,17-trioxospiro[2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-4,2'-oxirane]-7-yl] acetate;16958-30-8;4,8-Secosenecionan-8,11,16-trione, 15,20-dihydro-12-(acetyloxy)-15,20-epoxy-4-methyl-, (15-alpha,20S);C21H29NO8;C21-H29-N-O8;LS-144733

Suppliers and Price of Otosenine 12-acetate
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 4 raw suppliers
Chemical Property of Otosenine 12-acetate
Chemical Property:
  • Vapor Pressure:1.34E-15mmHg at 25°C 
  • Boiling Point:626.3°Cat760mmHg 
  • Flash Point:332.6°C 
  • PSA:111.74000 
  • Density:1.27g/cm3 
  • LogP:0.72940 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:9
  • Rotatable Bond Count:2
  • Exact Mass:423.18931688
  • Heavy Atom Count:30
  • Complexity:792
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1CC2(C(O2)C)C(=O)OC3CCN(CC=C(C3=O)COC(=O)C1(C)OC(=O)C)C
  • Isomeric SMILES:C[C@@H]1CC2([C@@H](O2)C)C(=O)O[C@@H]3CCN(C/C=C(\C3=O)/COC(=O)[C@]1(C)OC(=O)C)C
Technology Process of Otosenine 12-acetate

There total 1 articles about Otosenine 12-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:
Guidance literature:
Otosenin, Acetylchlorid;
DOI:10.1021/jo01273a047
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