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CAS

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274692-75-0

2,5-di-O-benzyl-1,6-O-isopropylidene-D-allo-inositol 3,4-cyclic sulfate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 274692-75-0 Structure

  • Basic information

    1. Product Name: 2,5-di-O-benzyl-1,6-O-isopropylidene-D-allo-inositol 3,4-cyclic sulfate
    2. Synonyms: 2,5-di-O-benzyl-1,6-O-isopropylidene-D-allo-inositol 3,4-cyclic sulfate
    3. CAS NO:274692-75-0
    4. Molecular Formula:
    5. Molecular Weight: 462.521
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 274692-75-0.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: 2,5-di-O-benzyl-1,6-O-isopropylidene-D-allo-inositol 3,4-cyclic sulfate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,5-di-O-benzyl-1,6-O-isopropylidene-D-allo-inositol 3,4-cyclic sulfate(274692-75-0)
    11. EPA Substance Registry System: 2,5-di-O-benzyl-1,6-O-isopropylidene-D-allo-inositol 3,4-cyclic sulfate(274692-75-0)

  • 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: 274692-75-0(Hazardous Substances Data)

274692-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 274692-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,4,6,9 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 274692-75:
(8*2)+(7*7)+(6*4)+(5*6)+(4*9)+(3*2)+(2*7)+(1*5)=180
180 % 10 = 0
So 274692-75-0 is a valid CAS Registry Number.

274692-75-0Relevant articles and documents

Stereoselective synthesis of carba- and C-glycosyl analogs of fucopyranosides

Carpintero, Mercedes,Jaramillo, Carlos,Fernandez-Mayoralas, Alfonso

, p. 1285 - 1296 (2007/10/03)

Fucopyranoside analogs with methylene groups instead of endo- or exo- anomeric oxygens, carba- and C-fucopyranosides, respectively, were synthesized. For the synthesis of 5a-carba-L-fucose (1) two approaches were studied, which shared a common cyclitol bu

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