1N-(tert-butoxycarbonyl-6-aminohexanoyl)-2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamine

Base Information

Chemical Name:1N-(tert-butoxycarbonyl-6-aminohexanoyl)-2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamine
CAS No.:263762-44-3
Molecular Formula:C₂₅H₄₀N₂O₁₂
Molecular Weight:560.599
Hs Code.:

Synonyms:1N-(tert-butoxycarbonyl-6-aminohexanoyl)-2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1N-(tert-butoxycarbonyl-6-aminohexanoyl)-2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamine

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:: SDS file from LookChem

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Technology Process of 1N-(tert-butoxycarbonyl-6-aminohexanoyl)-2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamine

There total 1 articles about 1N-(tert-butoxycarbonyl-6-aminohexanoyl)-2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamine 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: 78.0%

: 6404-29-1
6-(tert-butoxycarbonylamino)hexanoic acid

: 14152-97-7,18866-59-6,93221-21-7,121959-10-2,121959-11-3,122564-52-7,41135-18-6
2,3,4,6-tetra-O-Acetyl-β-D-galactopyranosyl isothiocyanate

: 263762-44-3
1N-(tert-butoxycarbonyl-6-aminohexanoyl)-2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamine

Guidance literature:: With triethylamine; In toluene; at 20 ℃; for 48h;
DOI:10.1016/S0040-4039(99)02216-9

Reference yield:

: 263762-44-3
1N-(tert-butoxycarbonyl-6-aminohexanoyl)-2,3,4,6-tetra-O-acetyl-β-D-galactopyranosylamine

: 38822-56-9,52116-51-5
N-(ε-aminocaproyl)-β-D-galactopyranosylamine

Guidance literature:: Multi-step reaction with 2 steps

1: NaOH / methanol

2: TFA

With sodium hydroxide; trifluoroacetic acid; In methanol; 1: Deacetylation / 2: deacylation;
DOI:10.1016/S0040-4039(99)02216-9