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CAS

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929619-07-8

allyl 3,4,6-tri-O-benzyl-2-O-p-methoxybenzyl-β-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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  • 929619-07-8 Structure

  • Basic information

    1. Product Name: allyl 3,4,6-tri-O-benzyl-2-O-p-methoxybenzyl-β-D-glucopyranoside
    2. Synonyms: allyl 3,4,6-tri-O-benzyl-2-O-p-methoxybenzyl-β-D-glucopyranoside
    3. CAS NO:929619-07-8
    4. Molecular Formula:
    5. Molecular Weight: 610.747
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 929619-07-8.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 3,4,6-tri-O-benzyl-2-O-p-methoxybenzyl-β-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: allyl 3,4,6-tri-O-benzyl-2-O-p-methoxybenzyl-β-D-glucopyranoside(929619-07-8)
    11. EPA Substance Registry System: allyl 3,4,6-tri-O-benzyl-2-O-p-methoxybenzyl-β-D-glucopyranoside(929619-07-8)

  • 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: 929619-07-8(Hazardous Substances Data)

929619-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 929619-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,6,1 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 929619-07:
(8*9)+(7*2)+(6*9)+(5*6)+(4*1)+(3*9)+(2*0)+(1*7)=208
208 % 10 = 8
So 929619-07-8 is a valid CAS Registry Number.

929619-07-8Relevant articles and documents

Development of adamantan-1-yl-methoxy-functionalized 1-deoxynojirimycin derivatives as selective inhibitors of glucosylceramide metabolism in man

Wennekes, Tom,Van Den Berg, Richard J. B. H. N.,Donker, Wilma,Van Der Marel, Gijsbert A.,Strijland, Anneke,Aerts, Johannes M. F. G.,Overkleeft, Herman S.

, p. 1088 - 1097 (2007/10/03)

(Chemical Equation Presented) In this article, we present a straightforward synthesis of adamantan-1-yl-methoxy-functionalized 1-deoxynojirimycin derivatives. The used synthetic routes are flexible and can be used to create a wide variety of lipophilic mo

Deoxynojirimycin analogues and their uses as glucosylceramidase inhibitors

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Page/Page column 8; 29, (2008/06/13)

The invention provides a new class of deoxynojirimycin analogues, or pharmaceutically acceptable salts thereof which can suitably be used for the treatment of a disease selected from the group consisting of insulin resistance, Gauger disease, inflammatory

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