D-Galactitol, 1,5-anhydro-1-C-(1,3-diphenyl-2-imidazolidinyl)-6-O-(triphenylmethyl)-, (1S)-

Base Information

Chemical Name:D-Galactitol, 1,5-anhydro-1-C-(1,3-diphenyl-2-imidazolidinyl)-6-O-(triphenylmethyl)-, (1S)-
CAS No.:228115-88-6
Molecular Formula:C40H40 N2 O5
Molecular Weight:0
Hs Code.:

Synonyms:D-Galactitol, 1,5-anhydro-1-C-(1,3-diphenyl-2-imidazolidinyl)-6-O-(triphenylmethyl)-, (1S)-

Suppliers and Price of D-Galactitol, 1,5-anhydro-1-C-(1,3-diphenyl-2-imidazolidinyl)-6-O-(triphenylmethyl)-, (1S)-

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 1 raw suppliers

Chemical Property of D-Galactitol, 1,5-anhydro-1-C-(1,3-diphenyl-2-imidazolidinyl)-6-O-(triphenylmethyl)-, (1S)-

Chemical Property:

PSA：85.63000
LogP:5.32810

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of D-Galactitol, 1,5-anhydro-1-C-(1,3-diphenyl-2-imidazolidinyl)-6-O-(triphenylmethyl)-, (1S)-

There total 3 articles about D-Galactitol, 1,5-anhydro-1-C-(1,3-diphenyl-2-imidazolidinyl)-6-O-(triphenylmethyl)-, (1S)- 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:

: 52443-07-9
3,4,5,7-tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptonitrile

: 228115-88-6
1,3-diphenyl-2-(6-O-triphenylmethyl-β-D-galactopyranosyl)-imidazolidine

Guidance literature:: Multi-step reaction with 3 steps

1: NaH₂PO₂ / Raney nickel

2: sodium methoxide / methanol / 3 h

3: 1.93 g / triethylamine / CH₂Cl₂

With sodium hypophosphite; sodium methylate; triethylamine; nickel; In methanol; dichloromethane; 1: Reduction / 2: Deacetylation / 3: Etherification;
DOI:10.1016/S0040-4020(99)00327-0

Reference yield:

: 71420-08-1
1,3-diphenyl-2-(tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptosyl)imidazolidine

: 228115-88-6
1,3-diphenyl-2-(6-O-triphenylmethyl-β-D-galactopyranosyl)-imidazolidine

Guidance literature:: Multi-step reaction with 2 steps

1: sodium methoxide / methanol / 3 h

2: 1.93 g / triethylamine / CH₂Cl₂

With sodium methylate; triethylamine; In methanol; dichloromethane; 1: Deacetylation / 2: Etherification;
DOI:10.1016/S0040-4020(99)00327-0