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CAS

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102235-57-4

3,4,5-Tri-O-benzyl-2,6-didesoxy-D-ribo-aldehydo-hexose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102235-57-4 Structure

  • Basic information

    1. Product Name: 3,4,5-Tri-O-benzyl-2,6-didesoxy-D-ribo-aldehydo-hexose
    2. Synonyms: 3,4,5-Tri-O-benzyl-2,6-didesoxy-D-ribo-aldehydo-hexose
    3. CAS NO:102235-57-4
    4. Molecular Formula:
    5. Molecular Weight: 418.533
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102235-57-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,4,5-Tri-O-benzyl-2,6-didesoxy-D-ribo-aldehydo-hexose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4,5-Tri-O-benzyl-2,6-didesoxy-D-ribo-aldehydo-hexose(102235-57-4)
    11. EPA Substance Registry System: 3,4,5-Tri-O-benzyl-2,6-didesoxy-D-ribo-aldehydo-hexose(102235-57-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 102235-57-4(Hazardous Substances Data)

102235-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102235-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,3 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 102235-57:
(8*1)+(7*0)+(6*2)+(5*2)+(4*3)+(3*5)+(2*5)+(1*7)=74
74 % 10 = 4
So 102235-57-4 is a valid CAS Registry Number.

102235-57-4Relevant articles and documents

A general route to 4-C-branched sugars. Synthesis of methyl α-caryophylloside

Prandi, Jacques

, p. 241 - 247 (2001)

The total synthesis of methyl 3,6-dideoxy-4-C-(D-altro-1,3,4,5 tetrahydroxyhexyl)-α-D-xylo-hexopyranoside, the methyl glycoside of the recently isolated 4-C-branched sugar caryophyllose, has been completed in a stereoselective and convergent manner. The synthesis of this dodecose relies on the diiodosamarium mediated coupling of two six-carbon fragments: a cyclic ketone and an acid chloride.

Synthesis of methyl α-caryophylloside

Prandi, Jacques,Couturier, Gwéna?lle

, p. 49 - 52 (2007/10/03)

The convergent synthesis of caryophyllose, a new C-4 branched dodecose isolated from Pseudomonas caryophylli, is described from two monosaccharidic precursors. The key step is the diiodosamarium-promoted coupling of two six-carbon fragments: an acid chloride and a cyclic ketone.

De novo Synthesis of Carbohydrates and Related Natural Products, 22. - Synthesis of D-Digitoxose from meso-Divinylglycol

Kuefner, Ulrike,Schmidt, Richard R.

, p. 1600 - 1609 (2007/10/02)

Selective monobenzylation of meso- and rac-divinylglycol (2-m and 2-d,l) affords racemates (+/-)-8 and (+/-)-10, respectively; they are transferred with the help of the Sharpless method under kinetic racemate resolution diastereoselectively into the enant

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