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1025071-10-6

C40H48O11 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1025071-10-6 Structure

  • Basic information

    1. Product Name: C40H48O11
    2. Synonyms: C40H48O11
    3. CAS NO:1025071-10-6
    4. Molecular Formula:
    5. Molecular Weight: 704.815
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1025071-10-6.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: C40H48O11(CAS DataBase Reference)
    10. NIST Chemistry Reference: C40H48O11(1025071-10-6)
    11. EPA Substance Registry System: C40H48O11(1025071-10-6)

  • 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: 1025071-10-6(Hazardous Substances Data)

1025071-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1025071-10-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,0,7 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1025071-10:
(9*1)+(8*0)+(7*2)+(6*5)+(5*0)+(4*7)+(3*1)+(2*1)+(1*0)=86
86 % 10 = 6
So 1025071-10-6 is a valid CAS Registry Number.

1025071-10-6Downstream Products

1025071-10-6Relevant articles and documents

Selective acetolysis of 6-deoxy-sugar oligosaccharide building blocks governed by the armed-disarmed effect

Bedini, Emiliano,Comegna, Daniela,Nola, Annalida Di,Parrilli, Michelangelo

, p. 2546 - 2551 (2008/09/21)

The effect of the arming-disarming protection in the acetolysis of 6-deoxy-sugar oligosaccharides has been for the first time systematically investigated. Starting from the newly synthesized methyl glycosides, the acetolysis conditions employed here afforded 1-O-Ac oligosaccharides selectively without cleavage of the interglycosidic bonds, if a suitable protecting group pattern was used. Actually, the behavior of armed-disarmed, armed-armed, and disarmed-disarmed 6-deoxy-sugar disaccharides in acetolysis reactions was investigated: the results fit well with the prediction made on the basis of the armed-disarmed effect.

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