PhenylMethyl 2-O-[2-(AcetylaMino)-2-deoxy-D-glucopyranosyl]-α-D-Mannopyranoside

Base Information

Chemical Name:PhenylMethyl 2-O-[2-(AcetylaMino)-2-deoxy-D-glucopyranosyl]-α-D-Mannopyranoside
CAS No.:436853-00-8
Molecular Formula:C₂₁H₃₁NO₁₁
Molecular Weight:473.477
Hs Code.:
Mol file:436853-00-8.mol

Synonyms:Benzyl 2-O-[2-(AcetylaMino)-2-deoxy-β-D-glucopyranosyl]-α-D-Mannopyranoside;GlcNAc(β1-2)Man(α1-)O-benzyl;PhenylMethyl 2-O-[2-(AcetylaMino)-2-deoxy-D-glucopyranosyl]-α-D-Mannopyranoside

Suppliers and Price of PhenylMethyl 2-O-[2-(AcetylaMino)-2-deoxy-D-glucopyranosyl]-α-D-Mannopyranoside

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

TRC
Benzyl2-O-[2-(Acetylamino)-2-deoxy-β-D-glucopyranosyl]-α-D-mannopyranoside
25mg
$ 5225.00

Total 2 raw suppliers

Chemical Property of PhenylMethyl 2-O-[2-(AcetylaMino)-2-deoxy-D-glucopyranosyl]-α-D-Mannopyranoside

Chemical Property:

PSA：190.89000
LogP:-2.18860

Purity/Quality:

95% ^*data from raw suppliers

Benzyl2-O-[2-(Acetylamino)-2-deoxy-β-D-glucopyranosyl]-α-D-mannopyranoside ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses A product formed from Benzyl α-D-mannopyranoside (B282000) by α-3-D-mannoside by the enzyme UDP-GlcNAc:α-3-D-mannoside β1,2-N-acetylglucosaminyltransferase I.2 in humans.

Technology Process of PhenylMethyl 2-O-[2-(AcetylaMino)-2-deoxy-D-glucopyranosyl]-α-D-Mannopyranoside

There total 1 articles about PhenylMethyl 2-O-[2-(AcetylaMino)-2-deoxy-D-glucopyranosyl]-α-D-Mannopyranoside 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:

: 15548-45-5
(2S,3S,4S,5S,6R)-2-benzyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

: 528-04-1,2616-63-9,7277-98-7,16465-33-1,19014-00-7,26234-54-8,26575-17-7,27963-82-2,29217-44-5,125639-14-7,16426-39-4,28508-02-3,5547-44-4,83332-40-5
uridine 5'-diphospho-N-acetylglucosamine

: 436853-00-8
C₂₁H₃₁NO₁₁

Guidance literature:: With N-Acetyl-D-glucosamine; recombinant human protein O-linked mannose β1,2-N-acetylgucosaminyltransferase 1 (Ser66-Thr660); AMP; manganese(ll) chloride; In glycerol; at 37 ℃; for 1h; pH=7; Kinetics; aq. MES buffer; Enzymatic reaction;
DOI:10.1016/j.bbrc.2011.06.042