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CAS

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213776-97-7

allyl (5,6,7,9-tetra-O-benzyl-1,2,3-trideoxy)-α-D-gluco-non-1-eno-4-ulopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 213776-97-7 Structure

  • Basic information

    1. Product Name: allyl (5,6,7,9-tetra-O-benzyl-1,2,3-trideoxy)-α-D-gluco-non-1-eno-4-ulopyranose
    2. Synonyms: allyl (5,6,7,9-tetra-O-benzyl-1,2,3-trideoxy)-α-D-gluco-non-1-eno-4-ulopyranose
    3. CAS NO:213776-97-7
    4. Molecular Formula:
    5. Molecular Weight: 620.786
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 213776-97-7.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: allyl (5,6,7,9-tetra-O-benzyl-1,2,3-trideoxy)-α-D-gluco-non-1-eno-4-ulopyranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: allyl (5,6,7,9-tetra-O-benzyl-1,2,3-trideoxy)-α-D-gluco-non-1-eno-4-ulopyranose(213776-97-7)
    11. EPA Substance Registry System: allyl (5,6,7,9-tetra-O-benzyl-1,2,3-trideoxy)-α-D-gluco-non-1-eno-4-ulopyranose(213776-97-7)

  • 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: 213776-97-7(Hazardous Substances Data)

213776-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 213776-97-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,7,7 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 213776-97:
(8*2)+(7*1)+(6*3)+(5*7)+(4*7)+(3*6)+(2*9)+(1*7)=147
147 % 10 = 7
So 213776-97-7 is a valid CAS Registry Number.

213776-97-7Relevant articles and documents

Inter- and intramolecular alcohol additions to exo-glycals

Chang, Chuan-Fa,Yang, Wen-Bin,Chang, Che-Chien,Lin, Chun-Hung

, p. 6515 - 6519 (2002)

Various exo-glycals were explored for the glycosidic bond formation and synthesis of spiroacetals in a stereoselective manner. The former reaction was an intermolecular alcohol addition to give the S new stereogenic center, resulting from the nucleophilic

Synthesis and elaboration of functionalised carbohydrate-derived spiroketals

Van Hooft, Peter A. V.,Oualid, Farid El,Overkleeft, Herman S.,Van der Marel, Gijsbert A.,Van Boom, Jacques H.,Leeuwenburgh, Michiel A.

, p. 1395 - 1403 (2007/10/03)

The scope of a stereoselective three-step approach for the synthesis of sugar derived spiroketals is presented. The methodology consists of Grignard addition of vinyl- or allylmagnesium bromide to a carbohydrate lactone, followed by K-10 clay mediated gly

A novel and flexible synthesis of pyranose spiroacetal derivatives

Van Hooft, Peter A. V.,Leeuwenburgh, Michiel A.,Overkleeft, Herman S.,Van Der Marel, Gijsbert A.,Van Boeckel, Constant A. A.,Van Boom, Jacques H.

, p. 6061 - 6064 (2007/10/03)

A three-step approach to chiral pyranose [5,4], [5,5], [5,6] and [5,7] unsaturated spiroacetal derivatives from perbenzylated glucopyranolactone 1 is presented. The strategy involves Grignard addition of vinyl or allyl magnesium bromide to 1 to give 2 and

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