tri-O-benzoyl-keto-D-erythro-1,3-dideoxy-[2]hexulose dimethyl dithioacetal

Base Information

Chemical Name:tri-O-benzoyl-keto-D-erythro-1,3-dideoxy-[2]hexulose dimethyl dithioacetal
CAS No.:22617-35-2
Molecular Formula:C₂₉H₃₀O₆S₂
Molecular Weight:538.686
Hs Code.:

tri-<i>O</i>-benzoyl-<i>keto</i>-<i>D</i>-<i>erythro</i>-1,3-dideoxy-[2]hexulose dimethyl dithioacetal

Synonyms:

Suppliers and Price of tri-O-benzoyl-keto-D-erythro-1,3-dideoxy-[2]hexulose dimethyl dithioacetal

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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 tri-O-benzoyl-keto-D-erythro-1,3-dideoxy-[2]hexulose dimethyl dithioacetal

Chemical Property:

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Technology Process of tri-O-benzoyl-keto-D-erythro-1,3-dideoxy-[2]hexulose dimethyl dithioacetal

There total 5 articles about tri-O-benzoyl-keto-D-erythro-1,3-dideoxy-[2]hexulose dimethyl dithioacetal 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:

: 124103-74-8
tri-O-benzoyl-aldehydo-D-erythro-2-deoxy-pentose

: 22617-35-2
tri-O-benzoyl-keto-D-erythro-1,3-dideoxy-[2]hexulose dimethyl dithioacetal

Guidance literature:: Multi-step reaction with 5 steps

1: NaHCO₃, Br₂ / H₂O; tetrahydrofuran

2: SOCl₂

3: diethyl ether

4: aq. HI / CHCl₃

5: HCl

With hydrogenchloride; thionyl chloride; hydrogen iodide; bromine; sodium hydrogencarbonate; In tetrahydrofuran; diethyl ether; chloroform; water;
DOI:10.1016/S0008-6215(00)82230-2

Reference yield:

: 22617-31-8
C₂₆H₂₂O₈

: 22617-35-2
tri-O-benzoyl-keto-D-erythro-1,3-dideoxy-[2]hexulose dimethyl dithioacetal

Guidance literature:: Multi-step reaction with 4 steps

1: SOCl₂

2: diethyl ether

3: aq. HI / CHCl₃

4: HCl

With hydrogenchloride; thionyl chloride; hydrogen iodide; In diethyl ether; chloroform;
DOI:10.1016/S0008-6215(00)82230-2

Reference yield:

: 22617-33-0
C₂₆H₂₁ClO₇

: 22617-35-2
tri-O-benzoyl-keto-D-erythro-1,3-dideoxy-[2]hexulose dimethyl dithioacetal

Guidance literature:: Multi-step reaction with 3 steps

1: diethyl ether

2: aq. HI / CHCl₃

3: HCl

With hydrogenchloride; hydrogen iodide; In diethyl ether; chloroform;
DOI:10.1016/S0008-6215(00)82230-2