methyl 3-S-acetyl-2-O-benzyl-4,6-O-benzylidene-3-thio-α-D-mannopyranoside

Base Information

Chemical Name:methyl 3-S-acetyl-2-O-benzyl-4,6-O-benzylidene-3-thio-α-D-mannopyranoside
CAS No.:183000-62-6
Molecular Formula:C₂₃H₂₆O₆S
Molecular Weight:430.522
Hs Code.:

Synonyms:methyl 3-S-acetyl-2-O-benzyl-4,6-O-benzylidene-3-thio-α-D-mannopyranoside

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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 methyl 3-S-acetyl-2-O-benzyl-4,6-O-benzylidene-3-thio-α-D-mannopyranoside

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Technology Process of methyl 3-S-acetyl-2-O-benzyl-4,6-O-benzylidene-3-thio-α-D-mannopyranoside

There total 2 articles about methyl 3-S-acetyl-2-O-benzyl-4,6-O-benzylidene-3-thio-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:

: 141115-75-5
methyl 2-O-benzyl-4,6-di-O-benzylidene-α-D-altropyranoside

: 183000-62-6
methyl 3-S-acetyl-2-O-benzyl-4,6-O-benzylidene-3-thio-α-D-mannopyranoside

: methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-benzyl-α-D-erythro-hex-2-enopyranoside

Guidance literature:: With pyridine; trifluorormethanesulfonic acid; potassium thioacetate; Yield given. Multistep reaction. Yields of byproduct given; 1.) CH₂Cl₂, 2.) CH₂Cl₂, DMF, RT, 48 h;
DOI:10.1002/jhet.5570330440

Reference yield:

: 141115-75-5
methyl 2-O-benzyl-4,6-di-O-benzylidene-α-D-altropyranoside

: 10387-40-3
potassium thioacetate

: 183000-62-6
methyl 3-S-acetyl-2-O-benzyl-4,6-O-benzylidene-3-thio-α-D-mannopyranoside

: methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-benzyl-α-D-erythro-hex-2-enopyranoside

Guidance literature:: With pyridine; trifluorormethanesulfonic acid; Yield given. Multistep reaction. Yields of byproduct given; 1.) CH₂Cl₂, 2.) CH₂Cl₂, DMF, RT, 48 h;
DOI:10.1002/jhet.5570330440