isopropyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranoside

Base Information

Chemical Name:isopropyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranoside
CAS No.:1198604-64-6
Molecular Formula:C₃₇H₃₃NO₁₀
Molecular Weight:651.67
Hs Code.:

Synonyms:isopropyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranoside

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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 isopropyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranoside

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Technology Process of isopropyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranoside

There total 2 articles about isopropyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranoside 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: 89.0%

: 82469-72-5
2Z-benzoyloxyimino-hexopyranosyl bromide

: 67-63-0,8013-70-5
isopropyl alcohol

: 1198604-64-6
isopropyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranoside

Guidance literature:: With silver (II) carbonate; In dichloromethane; at 20 ℃; for 2.5h; Molecular sieve; Darkness;
DOI:10.1016/j.carres.2009.08.007

Reference yield: 27.0%

: 98-88-4
benzoyl chloride

: 87713-52-8
isopropyl 3,4,6-tri-O-benzoyl-β-arabino-hexopyranosid-2-ulose

: 1198604-65-7
isopropyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranoside

: 1198604-64-6
isopropyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranoside

Guidance literature:: isopropyl 3,4,6-tri-O-benzoyl-β-arabino-hexopyranosid-2-ulose; With pyridine; hydroxylamine hydrochloride; In methanol; at 20 ℃; for 24h;

benzoyl chloride; With pyridine; In chloroform; at 20 ℃; for 24h;
DOI:10.1016/j.carres.2009.08.007