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Diphenyl(methoxy)methane

Base Information
  • Chemical Name:Diphenyl(methoxy)methane
  • CAS No.:1016-09-7
  • Molecular Formula:C14H14 O
  • Molecular Weight:198.265
  • Hs Code.:
  • Mol file:1016-09-7.mol
Diphenyl(methoxy)methane

Synonyms:Ether,diphenylmethyl methyl (6CI,7CI,8CI); Benzhydrol methyl ether; Benzhydryl methylether; Diphenylmethyl methyl ether; Methoxydiphenylmethane; NSC 75

Suppliers and Price of Diphenyl(methoxy)methane
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
  • Sigma-Aldrich
  • DIPHENYLMETHYL METHYL ETHER Aldrich
  • 50mg
  • $ 144.00
Total 15 raw suppliers
Chemical Property of Diphenyl(methoxy)methane
Chemical Property:
  • Boiling Point:270.6°Cat760mmHg 
  • Flash Point:122.6°C 
  • PSA:9.23000 
  • Density:1.03g/cm3 
  • LogP:3.42240 
Purity/Quality:

98%,99%, *data from raw suppliers

DIPHENYLMETHYL METHYL ETHER Aldrich *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Diphenyl(methoxy)methane

There total 150 articles about Diphenyl(methoxy)methane 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:
In methanol; for 2h; Quantum yield; Product distribution; Irradiation; irradiation in benzene solution;
DOI:10.1246/cl.1990.1079
Refernces

Hypervalent-iodine(iii) oxidation of hydrazones to diazo compounds and one-pot nickel(ii)-catalyzed cyclopropanation

10.1039/c5nj02378e

The study presents a novel one-pot method for the catalytic cyclopropanation of various alkenes with unsubstituted hydrazones. The process utilizes iodosobenzene as an oxidant to convert hydrazones into diazo compounds, which are then cyclopropanated in the presence of a nickel(II) catalyst, Ni(OH)2. This method allows for the efficient generation of cyclopropane products under mild conditions (80°C) within a short time frame (5 minutes to 4 hours) and with moderate to good yields (42–91%). The protocol is applicable to a wide range of substrates, including aryl alkenes with different electronic effects, aliphatic alkenes with halogen functional groups, and alkyl acrylates. The study also explores the reaction mechanism and provides a promising approach to synthesizing cyclopropane compounds, which are prevalent in natural products and have significant value in pharmaceutical chemistry.

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