1,2-Ethanediol, 1,2-bis(2-methylphenyl)-, (1R,2S)-rel-

Base Information

Chemical Name:1,2-Ethanediol, 1,2-bis(2-methylphenyl)-, (1R,2S)-rel-
CAS No.:34737-70-7
Molecular Formula:C₁₆H₁₈O₂
Molecular Weight:242.318
Hs Code.:
Mol file:34737-70-7.mol

Synonyms:meso-1,2-di(o-methylphenyl)ethane-1,2-diol;2,2'-Dimethyl-hydrobenzoin od. 1,2-Bis-(2-methyl-phenyl)-ethan-1,2-diol;

Suppliers and Price of 1,2-Ethanediol, 1,2-bis(2-methylphenyl)-, (1R,2S)-rel-

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 0 raw suppliers

Chemical Property of 1,2-Ethanediol, 1,2-bis(2-methylphenyl)-, (1R,2S)-rel-

Chemical Property:

Melting Point:111 - 116 °C
Boiling Point:406.6±40.0 °C(Predicted)
PSA：40.46000
Density:1.142±0.06 g/cm3(Predicted)
LogP:3.07040

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1,2-Ethanediol, 1,2-bis(2-methylphenyl)-, (1R,2S)-rel-

There total 29 articles about 1,2-Ethanediol, 1,2-bis(2-methylphenyl)-, (1R,2S)-rel- 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:

Reference yield: 93.0%

: 36888-18-3
(E)-2,2'-dimethylstilbene

: 34737-70-7,64158-25-4,104945-07-5,116204-38-7
threo-1,2-bis(2-methylphenyl)ethane-1,2-diol

Guidance literature:: (E)-2,2'-dimethylstilbene; With water; cyclopropane-1,1-dicarbonyl peroxide; In chloroform; at 40 ℃; for 24h;

With water; sodium hydroxide; at 60 ℃; for 4h; optical yield given as %de; diastereoselective reaction;
DOI:10.1021/ja1066674