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CAS

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1338782-77-6

C63H58O15 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1338782-77-6 Structure

  • Basic information

    1. Product Name: C63H58O15
    2. Synonyms: C63H58O15
    3. CAS NO:1338782-77-6
    4. Molecular Formula:
    5. Molecular Weight: 1055.14
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1338782-77-6.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: C63H58O15(CAS DataBase Reference)
    10. NIST Chemistry Reference: C63H58O15(1338782-77-6)
    11. EPA Substance Registry System: C63H58O15(1338782-77-6)

  • 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: 1338782-77-6(Hazardous Substances Data)

1338782-77-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338782-77-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,7,8 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1338782-77:
(9*1)+(8*3)+(7*3)+(6*8)+(5*7)+(4*8)+(3*2)+(2*7)+(1*7)=196
196 % 10 = 6
So 1338782-77-6 is a valid CAS Registry Number.

1338782-77-6Downstream Products

1338782-77-6Relevant articles and documents

Reducing the conformational flexibility of carbohydrates: Locking the 6-hydroxyl group by cyclopropanes

Brand, Christian,Granitzka, Markus,Stalke, Dietmar,Werz, Daniel B.

, p. 10782 - 10784 (2011/11/04)

The 6-hydroxyl group of hexopyranosides was stereochemically locked by the spiroannelation of a cyclopropane unit at C-5. The corresponding glucose and mannose derivatives were prepared and their behaviour in glycosidation reactions was studied.

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