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Cyclopentadecanone, 3-methyl-, (3R)-

Base Information
  • Chemical Name:Cyclopentadecanone, 3-methyl-, (3R)-
  • CAS No.:10403-00-6
  • Molecular Formula:C16H30 O
  • Molecular Weight:238.414
  • Hs Code.:2914299000
  • UNII:UPS3C6CV36
  • Nikkaji Number:J276.713I
  • Wikidata:Q27291190
  • ChEMBL ID:CHEMBL3731037
  • Mol file:10403-00-6.mol
Cyclopentadecanone, 3-methyl-, (3R)-

Synonyms:3-methylcyclopentadecanone;DL-3-methylcyclopentadecanone;muscone;muscone, (+-)-;muskone

Suppliers and Price of Cyclopentadecanone, 3-methyl-, (3R)-
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
  • TRC
  • (R)-Muscone
  • 100mg
  • $ 255.00
  • TRC
  • (R)-Muscone
  • 25mg
  • $ 110.00
  • AvaChem
  • (R)-(-)-Muscone
  • 100mg
  • $ 290.00
  • AvaChem
  • (R)-(-)-Muscone
  • 1g
  • $ 890.00
  • American Custom Chemicals Corporation
  • (R)-(-)-MUSCONE 95.00%
  • 5MG
  • $ 495.79
Total 34 raw suppliers
Chemical Property of Cyclopentadecanone, 3-methyl-, (3R)-
Chemical Property:
  • Vapor Pressure:0.000176mmHg at 25°C 
  • Boiling Point:329.5°C at 760 mmHg 
  • Flash Point:145.3°C 
  • PSA:17.07000 
  • Density:0.843g/cm3 
  • LogP:5.27650 
  • 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:

98%,99%, *data from raw suppliers

(R)-Muscone *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1CCCCCCCCCCCCC(=O)C1
  • Isomeric SMILES:C[C@@H]1CCCCCCCCCCCCC(=O)C1
  • General Description (R)-(-)-Muscone is a naturally occurring macrocyclic ketone with a musk-like odor, widely used in perfumery. It can be synthesized through various enantioselective methods, including copper-catalyzed conjugate additions, enantioselective protonation, ring-closing metathesis, and asymmetric methyl addition. Key synthetic strategies involve the use of chiral ligands or catalysts to achieve high enantiomeric excess (up to >95% ee), as demonstrated in methods such as the enantioselective protonation of a bicyclic ketone enolate or the copper-catalyzed 1,4-addition of dialkylzinc reagents to cyclic enones. (R)-(-)-MUSCONE is typically obtained as a C15 macrocycle, with ring-closing metathesis proving particularly efficient for its natural (R)-configuration.
Technology Process of Cyclopentadecanone, 3-methyl-, (3R)-

There total 160 articles about Cyclopentadecanone, 3-methyl-, (3R)- 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:
With hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1039/a802891e
Guidance literature:
With hydrogen; nickel; In ethyl acetate;
DOI:10.1002/ejoc.200400037
Guidance literature:
With hydrogen; palladium on activated charcoal; In ethanol; at 20 ℃; for 1h;
DOI:10.1271/bbb.66.1389
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