1-deoxy-1-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethoxyamino)-D-maltotriitol

Base Information

Chemical Name:1-deoxy-1-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethoxyamino)-D-maltotriitol
CAS No.:1141738-25-1
Molecular Formula:C₄₅H₆₅NO₁₉S
Molecular Weight:956.072
Hs Code.:

Synonyms:1-deoxy-1-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethoxyamino)-D-maltotriitol

Suppliers and Price of 1-deoxy-1-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethoxyamino)-D-maltotriitol

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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 1-deoxy-1-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethoxyamino)-D-maltotriitol

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Technology Process of 1-deoxy-1-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethoxyamino)-D-maltotriitol

There total 1 articles about 1-deoxy-1-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethoxyamino)-D-maltotriitol 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: 86.0%

: D-maltotriose O-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethyl)oxime

: 1141738-25-1
1-deoxy-1-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethoxyamino)-D-maltotriitol

Guidance literature:: With sodium cyanoborohydride; In acetic acid; at 20 ℃; for 2h;
DOI:10.1002/chem.200801521

Reference yield:

: 1141738-25-1
1-deoxy-1-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethoxyamino)-D-maltotriitol

: 50-99-7
D-glucose

: 1141738-24-0
1-deoxy-1-(2-(2-[2-(2-tritylsulfanylethoxy)ethoxy]ethoxy)ethoxyamino)-D-maltitol

Guidance literature:: With glucoamylase from Aspergillus niger; water; at 42 ℃; pH=7.0; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1002/chem.200801521