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871584-88-2

ethyl 6-O-benzyl-2-O-benzoyl-α-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 871584-88-2 Structure

  • Basic information

    1. Product Name: ethyl 6-O-benzyl-2-O-benzoyl-α-D-glucopyranoside
    2. Synonyms: ethyl 6-O-benzyl-2-O-benzoyl-α-D-glucopyranoside
    3. CAS NO:871584-88-2
    4. Molecular Formula:
    5. Molecular Weight: 402.444
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 871584-88-2.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: ethyl 6-O-benzyl-2-O-benzoyl-α-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 6-O-benzyl-2-O-benzoyl-α-D-glucopyranoside(871584-88-2)
    11. EPA Substance Registry System: ethyl 6-O-benzyl-2-O-benzoyl-α-D-glucopyranoside(871584-88-2)

  • 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: 871584-88-2(Hazardous Substances Data)

871584-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 871584-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,5,8 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 871584-88:
(8*8)+(7*7)+(6*1)+(5*5)+(4*8)+(3*4)+(2*8)+(1*8)=212
212 % 10 = 2
So 871584-88-2 is a valid CAS Registry Number.

871584-88-2Relevant articles and documents

A new route to 2-C- And 4-C-branched sugars by palladium-indium bromide-mediated carbonyl allylation

Norsikian, Stephanie,Lubineau, Andre

, p. 4089 - 4094 (2007/10/03)

Palladium-catalysed carbonyl allylations can be effectively applied to the regio- and diastereoselective synthesis of 2-C- and 4-C-branched sugars from allylic esters or carbonates via the formation of π-allylpalladium(II) intermediates and their reductiv

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