3,4,6-tri-O-benzoyl-2-(p-nitrobenzoyl)oximino-α-D-arabino-hexopyranosyl bromide

Base Information

Chemical Name:3,4,6-tri-O-benzoyl-2-(p-nitrobenzoyl)oximino-α-D-arabino-hexopyranosyl bromide
CAS No.:88773-34-6
Molecular Formula:C₃₄H₂₅BrN₂O₁₁
Molecular Weight:717.483
Hs Code.:

Synonyms:3,4,6-tri-O-benzoyl-2-(p-nitrobenzoyl)oximino-α-D-arabino-hexopyranosyl bromide

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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 3,4,6-tri-O-benzoyl-2-(p-nitrobenzoyl)oximino-α-D-arabino-hexopyranosyl bromide

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Technology Process of 3,4,6-tri-O-benzoyl-2-(p-nitrobenzoyl)oximino-α-D-arabino-hexopyranosyl bromide

There total 3 articles about 3,4,6-tri-O-benzoyl-2-(p-nitrobenzoyl)oximino-α-D-arabino-hexopyranosyl bromide 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: 91.0%

: 88773-32-4
1,5-anhydro-3,4,6-tri-O-benzoyl-D-fructose O-(p-nitrobenzoyl)oxime

: 88773-34-6
3,4,6-tri-O-benzoyl-2-(p-nitrobenzoyl)oximino-α-D-arabino-hexopyranosyl bromide

Guidance literature:: With N-Bromosuccinimide; In tetrachloromethane; Irradiation;

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 88773-34-6
3,4,6-tri-O-benzoyl-2-(p-nitrobenzoyl)oximino-α-D-arabino-hexopyranosyl bromide

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / pyridine / CH₂Cl₂ / 2 h / Ambient temperature

2: 91 percent / N-bromosuccinimide / CCl₄ / Irradiation

With pyridine; N-Bromosuccinimide; In tetrachloromethane; dichloromethane;

Reference yield:

: 82569-81-1
1,5-anhydro-3,4,6-tri-O-benzoyl-D-fructose oxime

: 88773-34-6
3,4,6-tri-O-benzoyl-2-(p-nitrobenzoyl)oximino-α-D-arabino-hexopyranosyl bromide

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / pyridine / CH₂Cl₂ / 2 h / Ambient temperature

2: 91 percent / N-bromosuccinimide / CCl₄ / Irradiation

With pyridine; N-Bromosuccinimide; In tetrachloromethane; dichloromethane;