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2-benzyl-5-methoxyphenol

Base Information
  • Chemical Name:2-benzyl-5-methoxyphenol
  • CAS No.:6965-78-2
  • Molecular Formula:C14H14 O2
  • Molecular Weight:214.264
  • Hs Code.:
2-benzyl-5-methoxyphenol

Synonyms:o-Cresol,5-methoxy-a-phenyl- (8CI);2-Benzyl-5-methoxyphenol; 6-Benzyl-3-methoxyphenol; NSC 63376

Suppliers and Price of 2-benzyl-5-methoxyphenol
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 7 raw suppliers
Chemical Property of 2-benzyl-5-methoxyphenol
Chemical Property:
  • Vapor Pressure:1.07E-05mmHg at 25°C 
  • Boiling Point:360.4°Cat760mmHg 
  • Flash Point:199.5°C 
  • Density:1.12g/cm3 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-benzyl-5-methoxyphenol

There total 12 articles about 2-benzyl-5-methoxyphenol 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 [(C6H6)(PCy3)(CO)RuH]+*BF4?; isopropyl alcohol; In 1,2-dichloro-ethane; at 120 ℃; for 8h; Schlenk technique; Inert atmosphere; Sealed tube;
DOI:10.1021/jacs.1c06887
Guidance literature:
With {RuCl(p-cymene)[(R,R)-(S,S)-PhTRAP]}Cl; hydrogen; In tetrahydrofuran; at 80 ℃; for 24h; under 38002.6 Torr; optical yield given as %ee; Inert atmosphere;
DOI:10.3390/molecules17066901
Guidance literature:
With [(C6H6)(PCy3)(CO)RuH]+*BF4?; cyclopentene; In chlorobenzene; at 120 ℃; Overall yield = ~ 20 %; regioselective reaction;
DOI:10.1002/ejoc.201403518
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