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1256770-26-9

methyl 4,6-O-(benzylidene-d1)-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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  • 1256770-26-9 Structure

  • Basic information

    1. Product Name: methyl 4,6-O-(benzylidene-d1)-α-D-glucopyranoside
    2. Synonyms: methyl 4,6-O-(benzylidene-d1)-α-D-glucopyranoside
    3. CAS NO:1256770-26-9
    4. Molecular Formula:
    5. Molecular Weight: 283.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1256770-26-9.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: methyl 4,6-O-(benzylidene-d1)-α-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4,6-O-(benzylidene-d1)-α-D-glucopyranoside(1256770-26-9)
    11. EPA Substance Registry System: methyl 4,6-O-(benzylidene-d1)-α-D-glucopyranoside(1256770-26-9)

  • 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: 1256770-26-9(Hazardous Substances Data)

1256770-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1256770-26-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,7,7 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1256770-26:
(9*1)+(8*2)+(7*5)+(6*6)+(5*7)+(4*7)+(3*0)+(2*2)+(1*6)=169
169 % 10 = 9
So 1256770-26-9 is a valid CAS Registry Number.

1256770-26-9Upstream product

1256770-26-9Relevant articles and documents

Reductive openings of benzylidene acetals revisited: A mechanistic scheme for regio- and stereoselectivity

Johnsson, Richard,Ohlin, Markus,Ellervik, Ulf

, p. 8003 - 8011 (2010)

Despite the importance of regioselective reductive openings of cyclic acetals, mechanistic details are scarce. In this study 4,6-O-benzylidene acetals were used as model compounds for deciphering the mechanism of regioselective openings using a variety of

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