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CAS

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874906-11-3

6-O-acetyl-2,3,4-tri-O-benzyl-1-C-methyl-α-D-glucopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 874906-11-3 Structure

  • Basic information

    1. Product Name: 6-O-acetyl-2,3,4-tri-O-benzyl-1-C-methyl-α-D-glucopyranose
    2. Synonyms: 6-O-acetyl-2,3,4-tri-O-benzyl-1-C-methyl-α-D-glucopyranose
    3. CAS NO:874906-11-3
    4. Molecular Formula:
    5. Molecular Weight: 506.596
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 874906-11-3.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: 6-O-acetyl-2,3,4-tri-O-benzyl-1-C-methyl-α-D-glucopyranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-O-acetyl-2,3,4-tri-O-benzyl-1-C-methyl-α-D-glucopyranose(874906-11-3)
    11. EPA Substance Registry System: 6-O-acetyl-2,3,4-tri-O-benzyl-1-C-methyl-α-D-glucopyranose(874906-11-3)

  • 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: 874906-11-3(Hazardous Substances Data)

874906-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874906-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,9,0 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 874906-11:
(8*8)+(7*7)+(6*4)+(5*9)+(4*0)+(3*6)+(2*1)+(1*1)=203
203 % 10 = 3
So 874906-11-3 is a valid CAS Registry Number.

874906-11-3Relevant articles and documents

Trifluoromethanesulfonic acid efficiently catalyzed the intramolecular glycosidation of 1-C-alkyl-D-hexopyranoses to form the anhydroketopyranoses having 6,8-dioxabicyclo[3.2.1]octane structures

Yamanoi, Takashi,Matsumura, Kazuhide,Matsuda, Sho,Oda, Yoshiki

, p. 2973 - 2977 (2005)

The intramolecular glycosidation of the 1-C-alkyl-D-hexopyranose derivatives to form the anhydroketopyranoses having 6,8-dioxabicyclo[3.2.1] octane structures was investigated. We synthesized several 1-C-alkyl-2,3,4-tri- O-benzyl-D-hexopyranoses and found

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