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(2R,4R)-4-Methyl-2-phenyloxolane

Base Information
  • Chemical Name:(2R,4R)-4-Methyl-2-phenyloxolane
  • CAS No.:38300-00-4
  • Molecular Formula:C11H14O
  • Molecular Weight:162.232
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90553979
  • Nikkaji Number:J427.622A
  • Wikidata:Q82434744
(2R,4R)-4-Methyl-2-phenyloxolane

Synonyms:DTXSID90553979;(2R,4R)-4-Methyl-2-phenyloxolane

Suppliers and Price of (2R,4R)-4-Methyl-2-phenyloxolane
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of (2R,4R)-4-Methyl-2-phenyloxolane
Chemical Property:
  • XLogP3:2.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:162.104465066
  • Heavy Atom Count:12
  • Complexity:138
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1CC(OC1)C2=CC=CC=C2
  • Isomeric SMILES:C[C@@H]1C[C@@H](OC1)C2=CC=CC=C2
Technology Process of (2R,4R)-4-Methyl-2-phenyloxolane

There total 27 articles about (2R,4R)-4-Methyl-2-phenyloxolane 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 dibutyltin; In tetrahydrofuran; at -55 ℃; for 13h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; sonochemical irradiation;
DOI:10.1021/ja00199a059
Guidance literature:
With dibutyltin; In tetrahydrofuran; at -55 ℃; for 13h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; sonochemical irradiation;
DOI:10.1021/ja00199a059
Guidance literature:
With tri-n-butyl-tin hydride; 2,2'-azobis(isobutyronitrile); In benzene; at 80 ℃; for 2h; Mechanism; The effect of the number of halogen atom on the diastereoselectivity was investigated.;
DOI:10.1016/S0040-4039(00)80085-4
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