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Cyclopentadecanone, 3-methyl-, (3S)-

Base Information
  • Chemical Name:Cyclopentadecanone, 3-methyl-, (3S)-
  • CAS No.:63975-98-4
  • Molecular Formula:C16H30O
  • Molecular Weight:238.414
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70428131
  • Nikkaji Number:J489.984I
  • Wikidata:Q82240916
Cyclopentadecanone, 3-methyl-, (3S)-

Synonyms:Cyclopentadecanone, 3-methyl-, (3S)-;(+)-Muscone;63975-98-4;SCHEMBL316736;(s)-3-methyl-cyclopentadecanone;DTXSID70428131;AKOS015911952

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Chemical Property of Cyclopentadecanone, 3-methyl-, (3S)-
Chemical Property:
  • XLogP3:6.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:238.229665576
  • Heavy Atom Count:17
  • Complexity:198
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1CCCCCCCCCCCCC(=O)C1
  • Isomeric SMILES:C[C@H]1CCCCCCCCCCCCC(=O)C1
Technology Process of Cyclopentadecanone, 3-methyl-, (3S)-

There total 80 articles about Cyclopentadecanone, 3-methyl-, (3S)- 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:
dimethyl zinc(II); 4-(cis-2,6-dimethylpiperidine)-(R)-dinaphthdioxaphosphepin; copper compound; In toluene;
cyclopentadec-2-en-1-one; In toluene; Product distribution / selectivity;
Guidance literature:
With hydrogen; Ru2Cl4[(R)Tol-BINAP]2(NEt3); In methanol; at 25 ℃; for 24h; under 36778.6 Torr; Inert atmosphere;
Guidance literature:
3-methylcyclopentadecanone; With (R)-1-phenyl-ethyl-amine; toluene-4-sulfonic acid; In tetrahydrofuran; at 70 ℃; for 4h; Inert atmosphere; Irradiation;
With hydrogenchloride; In ethanol; water; at 65 ℃; for 1.8h; enantioselective reaction;
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