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CAS

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102734-31-6

1-O-(4′-vinylphenyl)-2,3,4,6-tetra-O-acetyl-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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  • 102734-31-6 Structure

  • Basic information

    1. Product Name: 1-O-(4′-vinylphenyl)-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside
    2. Synonyms:
    3. CAS NO:102734-31-6
    4. Molecular Formula:
    5. Molecular Weight: 450.442
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102734-31-6.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: 1-O-(4′-vinylphenyl)-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-O-(4′-vinylphenyl)-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside(102734-31-6)
    11. EPA Substance Registry System: 1-O-(4′-vinylphenyl)-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside(102734-31-6)

  • 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: 102734-31-6(Hazardous Substances Data)

102734-31-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102734-31-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,3 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102734-31:
(8*1)+(7*0)+(6*2)+(5*7)+(4*3)+(3*4)+(2*3)+(1*1)=86
86 % 10 = 6
So 102734-31-6 is a valid CAS Registry Number.

102734-31-6Downstream Products

102734-31-6Relevant articles and documents

Copper-Catalyzed Anomeric O-Arylation of Carbohydrate Derivatives at Room Temperature

Verdelet, Tristan,Benmahdjoub, Sara,Benmerad, Belkacem,Alami, Mouad,Messaoudi, Samir

, p. 9226 - 9238 (2019)

Direct and practical anomeric O-arylation of sugar lactols with substituted arylboronic acids has been established. Using copper catalysis at room temperature under an air atmosphere, the protocol proved to be general, and a variety of aryl O-glycosides have been prepared in good to excellent yields. Furthermore, this approach was extended successfully to unprotected carbohydrates, including α-mannose, and it was demonstrated here how the interaction between carbohydrates and boronic acids can be combined with copper catalysis to achieve selective anomeric O-arylation.

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