(3R)-Methyl-4,6-O-benzyliden-3-C-cyan-2,3-didesoxy-α-D-erythro-hexopyranosid

Base Information

Chemical Name:(3R)-Methyl-4,6-O-benzyliden-3-C-cyan-2,3-didesoxy-α-D-erythro-hexopyranosid
CAS No.:99967-16-5
Molecular Formula:C₁₅H₁₇NO₄
Molecular Weight:275.304
Hs Code.:

Synonyms:(3R)-Methyl-4,6-O-benzyliden-3-C-cyan-2,3-didesoxy-α-D-erythro-hexopyranosid

Suppliers and Price of (3R)-Methyl-4,6-O-benzyliden-3-C-cyan-2,3-didesoxy-α-D-erythro-hexopyranosid

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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 (3R)-Methyl-4,6-O-benzyliden-3-C-cyan-2,3-didesoxy-α-D-erythro-hexopyranosid

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Technology Process of (3R)-Methyl-4,6-O-benzyliden-3-C-cyan-2,3-didesoxy-α-D-erythro-hexopyranosid

There total 1 articles about (3R)-Methyl-4,6-O-benzyliden-3-C-cyan-2,3-didesoxy-α-D-erythro-hexopyranosid 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: 10.0%

: 63598-31-2
methyl 4,6-O-(R)-benzylidene-2-deoxy-α-D-erythrohexopyranosid-3-ulose

: 38622-91-2,36635-61-7
[(p-methylphenyl)sulfonylmethyl]isonitrile

: 99967-16-5
(3R)-Methyl-4,6-O-benzyliden-3-C-cyan-2,3-didesoxy-α-D-erythro-hexopyranosid

: 99967-17-6
(3S)-Methyl-4,6-O-benzyliden-3-C-cyan-2,3-didesoxy-α-D-erythro-hexopyranosid

Guidance literature:: With potassium tert-butylate; In 1,2-dimethoxyethane; tert-butyl alcohol; at 0 ℃; for 1h;
DOI:10.1002/jlac.198619860403

Reference yield: 45.0%

: 99967-16-5
(3R)-Methyl-4,6-O-benzyliden-3-C-cyan-2,3-didesoxy-α-D-erythro-hexopyranosid

: 100100-72-9
(3R)-Methyl-4,6-O-benzyliden-2,3-didesoxy-3-C-formyl-α-D-erythro-hexopyranosid

Guidance literature:: With lithium aluminium tetrahydride; ethyl acetate; In diethyl ether; at 0 ℃; for 0.666667h;
DOI:10.1002/jlac.198619860403