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607364-83-0

allyl 2,6-di-O-benzoyl-3-O-tert-butyldimethylsilyl-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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  • 607364-83-0 Structure

  • Basic information

    1. Product Name: allyl 2,6-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-glucopyranoside
    2. Synonyms: allyl 2,6-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-glucopyranoside
    3. CAS NO:607364-83-0
    4. Molecular Formula:
    5. Molecular Weight: 542.701
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 607364-83-0.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: allyl 2,6-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: allyl 2,6-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-glucopyranoside(607364-83-0)
    11. EPA Substance Registry System: allyl 2,6-di-O-benzoyl-3-O-tert-butyldimethylsilyl-α-D-glucopyranoside(607364-83-0)

  • 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: 607364-83-0(Hazardous Substances Data)

607364-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 607364-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,3,6 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 607364-83:
(8*6)+(7*0)+(6*7)+(5*3)+(4*6)+(3*4)+(2*8)+(1*3)=160
160 % 10 = 0
So 607364-83-0 is a valid CAS Registry Number.

607364-83-0Relevant articles and documents

Synthesis of laminarin oligosaccharide derivatives having D-arabinofuranosyl side-chains

He, Hongmei,Gu, Guofeng,Du, Yuguo

, p. 275 - 283 (2003)

An efficient glycosylation strategy was applied in the synthesis of β-D-glucopyranosyl-(1→3)-[α-D-arabinopyranosyl-(1→4)] -β-D-glucopyranosyl-(1→3)-β-D-glucopyranosyl-(1→3) -[α-D-arabinopyranosyl-(1→6)]-D-glucopyranose to secure β-D-(1→3) glycosidic bond

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