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CAS

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30571-58-5

L-Fucose tetraacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 30571-58-5 Structure

  • Basic information

    1. Product Name: L-Fucose tetraacetate
    2. Synonyms: 6-Deoxy-L-galactose 2,3,4,5-tetraacetate;L-Fucose 2,3,4,5-tetraacetate
    3. CAS NO:30571-58-5
    4. Molecular Formula: C14H20O9
    5. Molecular Weight: 332.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30571-58-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: L-Fucose tetraacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-Fucose tetraacetate(30571-58-5)
    11. EPA Substance Registry System: L-Fucose tetraacetate(30571-58-5)

  • 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: 30571-58-5(Hazardous Substances Data)

30571-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30571-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,7 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30571-58:
(7*3)+(6*0)+(5*5)+(4*7)+(3*1)+(2*5)+(1*8)=95
95 % 10 = 5
So 30571-58-5 is a valid CAS Registry Number.

30571-58-5Relevant articles and documents

Sulfinyl hexose derivatives useful for glycosylation

-

, (2008/06/13)

Hexose derivatives are described which facilitate control over the stereochemistry of the glycosyl bond formed in the course of a solid phase glycosylation reaction. Methods for their use are also described.

Synthesis of daunosamine hydrochloride and intermediates used in its preparation

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, (2008/06/13)

A process for synthesizing daunosamine hydrochloride is disclosed. Intermediates useful for synthesizing daunosamine hydrochloride, and processes for preparing such intermediates, are also disclosed.

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