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3,4-di-O-acetyl-2,6-di-O-benzyl-D-glucopyranosyl dimethyl phosphite is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 264230-04-8 Structure
  • Basic information

    1. Product Name: 3,4-di-O-acetyl-2,6-di-O-benzyl-D-glucopyranosyl dimethyl phosphite
    2. Synonyms: 3,4-di-O-acetyl-2,6-di-O-benzyl-D-glucopyranosyl dimethyl phosphite
    3. CAS NO:264230-04-8
    4. Molecular Formula:
    5. Molecular Weight: 536.516
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 264230-04-8.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: 3,4-di-O-acetyl-2,6-di-O-benzyl-D-glucopyranosyl dimethyl phosphite(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-di-O-acetyl-2,6-di-O-benzyl-D-glucopyranosyl dimethyl phosphite(264230-04-8)
    11. EPA Substance Registry System: 3,4-di-O-acetyl-2,6-di-O-benzyl-D-glucopyranosyl dimethyl phosphite(264230-04-8)
  • 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: 264230-04-8(Hazardous Substances Data)

264230-04-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 264230-04-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,4,2,3 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 264230-04:
(8*2)+(7*6)+(6*4)+(5*2)+(4*3)+(3*0)+(2*0)+(1*4)=108
108 % 10 = 8
So 264230-04-8 is a valid CAS Registry Number.

264230-04-8Downstream Products

264230-04-8Relevant articles and documents

Convergent synthesis of adenophostin A analogues via a base replacement strategy

Marwood, Rachel D.,Shuto, Satoshi,Jenkins, David J.,Potter, Barry V. L.

, p. 219 - 220 (2000)

The first totally synthetic base-modified analogues of the natural product and potent D-myo-inositol 1,4,5-trisphosphate receptor agonist adenophostin A were efficiently synthesised from D-xylose and D-glucose using methodology employing base and surrogate base addition to a common disaccharide intermediate.

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