N-<2-O--glucoloyl>-L-α-aminobutanoyl-D-isoglutamine benzyl ester

Base Information

Chemical Name:N-<2-O--glucoloyl>-L-α-aminobutanoyl-D-isoglutamine benzyl ester
CAS No.:141989-33-5
Molecular Formula:C₈₅H₁₁₃N₅O₁₆
Molecular Weight:1460.86
Hs Code.:

N-<2-O-<benzyl 2-acetamido-6-O-benzyl-4-O-(3,4,6-tri-O-benzyl-2-deoxy-2-stearoylamino-β-D-glucopyranosyl)-2,3-dideoxy-α-D-glucopyranosid-3-yl>-glucoloyl>-L-α-aminobutanoyl-D-isoglutamine benzyl ester

Synonyms:N-<2-O--glucoloyl>-L-α-aminobutanoyl-D-isoglutamine benzyl ester

Suppliers and Price of N-<2-O--glucoloyl>-L-α-aminobutanoyl-D-isoglutamine benzyl ester

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 N-<2-O--glucoloyl>-L-α-aminobutanoyl-D-isoglutamine benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-<2-O--glucoloyl>-L-α-aminobutanoyl-D-isoglutamine benzyl ester

There total 2 articles about N-<2-O--glucoloyl>-L-α-aminobutanoyl-D-isoglutamine benzyl ester 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: 69.0%

: N-[2-O-(benzyl 2-amino-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl-(1→4)-2-acetamido-6-O-benzyl-2,3-deoxy-α-D-glucopyranosid-3-yl)-glycoloyl]-L-α-aminobutanoyl-D-isoglutamine benzyl ester

: 112-76-5
Stearoyl chloride

: 141989-33-5
N-<2-O--glucoloyl>-L-α-aminobutanoyl-D-isoglutamine benzyl ester

Guidance literature:: With dmap; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 60 ℃; for 5h; chemoselective reaction;
DOI:10.1021/acs.jmedchem.7b00593

Reference yield:

: 112302-93-9
L-2-Aminobutanoyl-D-isoglutamine benzyl ester trifluoroacetate

: 141989-32-4
benzyl 2-acetamido-6-O-benzyl-4-O-(3,4,6-tri-O-benzyl-2-deoxy-2-stearoylamino-β-D-glucopyranosyl)-2-deoxy-3-O-carboxymethyl-α-D-glucopyranoside

: 141989-33-5
N-<2-O--glucoloyl>-L-α-aminobutanoyl-D-isoglutamine benzyl ester

Guidance literature:: With 1-hydroxybenzotriazol-hydrate; triethylamine; dicyclohexyl-carbodiimide; Yield given. Multistep reaction; 1.) CH₂Cl₂, 1 h, 2.) a) CH₂Cl₂, dioxane, 0 deg C, 2 h, b) CH₂Cl₂, dioxane, RT, 12 h;
DOI:10.1135/cccc19920579