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455333-50-3

allyl 2,4-di-O-benzoyl-α-D-fucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 455333-50-3 Structure

  • Basic information

    1. Product Name: allyl 2,4-di-O-benzoyl-α-D-fucopyranoside
    2. Synonyms: allyl 2,4-di-O-benzoyl-α-D-fucopyranoside
    3. CAS NO:455333-50-3
    4. Molecular Formula:
    5. Molecular Weight: 412.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 455333-50-3.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: allyl 2,4-di-O-benzoyl-α-D-fucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: allyl 2,4-di-O-benzoyl-α-D-fucopyranoside(455333-50-3)
    11. EPA Substance Registry System: allyl 2,4-di-O-benzoyl-α-D-fucopyranoside(455333-50-3)

  • 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: 455333-50-3(Hazardous Substances Data)

455333-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 455333-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,5,3,3 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 455333-50:
(8*4)+(7*5)+(6*5)+(5*3)+(4*3)+(3*3)+(2*5)+(1*0)=143
143 % 10 = 3
So 455333-50-3 is a valid CAS Registry Number.

455333-50-3Relevant articles and documents

Synthesis of the pentasaccharide hapten from the glycopeptidolipid antigen of Mycobacterium avium serovar 12

Varga, Zsolt,Bajza, István,Batta, Gyula,Lipták, András

, p. 3145 - 3148 (2002)

An effective synthesis of the pentasaccharide hapten from the glycopeptidolipid antigen of Mycobacterium avium serovar 12 in the protected p-nitrophenyl glycoside, using a 3+2 block synthesis strategy, is described.

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