.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2,4-bis-O-(phenylmethyl)-

Base Information

Chemical Name:.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2,4-bis-O-(phenylmethyl)-
CAS No.:85028-66-6
Molecular Formula:C20H22O4
Molecular Weight:326.39
Hs Code.:

Synonyms:.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2,4-bis-O-(phenylmethyl)-

Suppliers and Price of .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2,4-bis-O-(phenylmethyl)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 3 raw suppliers

Chemical Property of .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2,4-bis-O-(phenylmethyl)-

Chemical Property:

Melting Point:54 - 56 °C
PSA：36.92000
LogP:3.30240

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2,4-bis-O-(phenylmethyl)-

There total 4 articles about .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2,4-bis-O-(phenylmethyl)- 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: 78.0%

: 121633-37-2
1,6-anhydro-2,4-di-O-benzyl-3-O-(S-methylthiocarbonyl)-β-D-glucopyranose

: 85028-66-6
1,6-anhydro-2,4-di-O-benzyl-3-deoxy-β-D-ribohexapyranose

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; for 2h; Heating;

Reference yield:

: 33208-48-9
1,6 anhydro-2,4-di-O-benzyl-β-D-glucopyranose

: 85028-66-6
1,6-anhydro-2,4-di-O-benzyl-3-deoxy-β-D-ribohexapyranose

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) imidazole, NaH / 1.) THF, 50 deg C, 2.5 h, 2.) THF, RT, 30 min

2: tetrahydrofuran / Ambient temperature

3: 78 percent / Bu₃SnH, azobisisobutyronitrile / toluene / 2 h / Heating

With 1H-imidazole; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; sodium hydride; In tetrahydrofuran; toluene;

Reference yield:

: Dithiocarbonic acid O-((1R,2R,3S,4R,5R)-2,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-3-yl) ester

: 85028-66-6
1,6-anhydro-2,4-di-O-benzyl-3-deoxy-β-D-ribohexapyranose

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / Ambient temperature

2: 78 percent / Bu₃SnH, azobisisobutyronitrile / toluene / 2 h / Heating

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In tetrahydrofuran; toluene;