2,3-di-O-acetyl-N-benzyloxycarbonyl-4,6-di-O-(p-tolylsulfonyl)-5a-carba-D-glucopyranosylamine

Base Information

Chemical Name:2,3-di-O-acetyl-N-benzyloxycarbonyl-4,6-di-O-(p-tolylsulfonyl)-5a-carba-D-glucopyranosylamine
CAS No.:191723-81-6
Molecular Formula:C₃₃H₃₇NO₁₂S₂
Molecular Weight:703.788
Hs Code.:

Synonyms:2,3-di-O-acetyl-N-benzyloxycarbonyl-4,6-di-O-(p-tolylsulfonyl)-5a-carba-D-glucopyranosylamine

Suppliers and Price of 2,3-di-O-acetyl-N-benzyloxycarbonyl-4,6-di-O-(p-tolylsulfonyl)-5a-carba-D-glucopyranosylamine

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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 2,3-di-O-acetyl-N-benzyloxycarbonyl-4,6-di-O-(p-tolylsulfonyl)-5a-carba-D-glucopyranosylamine

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

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Technology Process of 2,3-di-O-acetyl-N-benzyloxycarbonyl-4,6-di-O-(p-tolylsulfonyl)-5a-carba-D-glucopyranosylamine

There total 3 articles about 2,3-di-O-acetyl-N-benzyloxycarbonyl-4,6-di-O-(p-tolylsulfonyl)-5a-carba-D-glucopyranosylamine 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:

: 89859-47-2
(1R)-(1,3,4/2,6)-1,7-O-benzylidene-4-<(benzyloxycarbonyl)amino>-6-C-(hydroxymethyl)-1,2,3-cyclohexanetriol

: 191723-81-6
2,3-di-O-acetyl-N-benzyloxycarbonyl-4,6-di-O-(p-tolylsulfonyl)-5a-carba-D-glucopyranosylamine

Guidance literature:: Multi-step reaction with 3 steps

1: 89.6 percent / pyridine / 8 h / Ambient temperature

2: 0.5 N HCl / methanol / 0.5 h / Heating

3: 4.5 g / pyridine; CH₂Cl₂ / 14 h / Ambient temperature

With hydrogenchloride; In pyridine; methanol; dichloromethane;
DOI:10.1016/S0008-6215(97)00052-9

Reference yield:

: 2,3-di-O-acetyl-4,6-O-benzylidene-N-benzyloxycarbonyl-5a-carba-D-glucopyranosylamine

: 191723-81-6
2,3-di-O-acetyl-N-benzyloxycarbonyl-4,6-di-O-(p-tolylsulfonyl)-5a-carba-D-glucopyranosylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 0.5 N HCl / methanol / 0.5 h / Heating

2: 4.5 g / pyridine; CH₂Cl₂ / 14 h / Ambient temperature

With hydrogenchloride; In pyridine; methanol; dichloromethane;
DOI:10.1016/S0008-6215(97)00052-9