N-octyl-N-trifluoroacetyl-4,6-O-benzylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine

Base Information

Chemical Name:N-octyl-N-trifluoroacetyl-4,6-O-benzylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine
CAS No.:442852-04-2
Molecular Formula:C₂₄H₃₂F₃NO₅
Molecular Weight:471.517
Hs Code.:

Synonyms:N-octyl-N-trifluoroacetyl-4,6-O-benzylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine

Suppliers and Price of N-octyl-N-trifluoroacetyl-4,6-O-benzylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of N-octyl-N-trifluoroacetyl-4,6-O-benzylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of N-octyl-N-trifluoroacetyl-4,6-O-benzylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine

There total 3 articles about N-octyl-N-trifluoroacetyl-4,6-O-benzylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine 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:

: 177898-40-7
N-octyl-2,3:4,6-di-O-isopropylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine

: 442852-04-2
N-octyl-N-trifluoroacetyl-4,6-O-benzylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / pyridine / 1 h / 20 °C

2: AcOH / H₂O / 0.5 h / 80 °C

3: 1.96 g / dimethylformamide / 2 h / 45 °C

With acetic acid; In pyridine; water; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(02)00005-6

Reference yield:

: 442851-94-7
N-octyl-N-trifluoroacetyl-2,3:4,6-di-O-isopropylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine

: 442852-04-2
N-octyl-N-trifluoroacetyl-4,6-O-benzylidene-5a-carba-β-D-xylo-hex-5(5a)-enopyranosylamine

Guidance literature:: Multi-step reaction with 2 steps

1: AcOH / H₂O / 0.5 h / 80 °C

2: 1.96 g / dimethylformamide / 2 h / 45 °C

With acetic acid; In water; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(02)00005-6