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CAS

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1006726-12-0

N-(2-pivaloyloxyethyl)-p-toluenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1006726-12-0 Structure

  • Basic information

    1. Product Name: N-(2-pivaloyloxyethyl)-p-toluenesulfonamide
    2. Synonyms:
    3. CAS NO:1006726-12-0
    4. Molecular Formula:
    5. Molecular Weight: 299.391
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1006726-12-0.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: N-(2-pivaloyloxyethyl)-p-toluenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-pivaloyloxyethyl)-p-toluenesulfonamide(1006726-12-0)
    11. EPA Substance Registry System: N-(2-pivaloyloxyethyl)-p-toluenesulfonamide(1006726-12-0)

  • 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: 1006726-12-0(Hazardous Substances Data)

1006726-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1006726-12-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,7,2 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1006726-12:
(9*1)+(8*0)+(7*0)+(6*6)+(5*7)+(4*2)+(3*6)+(2*1)+(1*2)=110
110 % 10 = 0
So 1006726-12-0 is a valid CAS Registry Number.

1006726-12-0Relevant articles and documents

Synthesis and antiviral properties of aza-analogues of Acyclovir

Koszytkowska-Stawinska, Mariola,Kaleta, Katarzyna,Sas, Wojciech,De Clercq, Erik

, p. 51 - 64 (2007)

Aza-analogues of Acyclovir were obtained from N-(2-pivaloyloxyethyl)-N- (pivaloyloxymethyl)-p-toluenesulfonamide via a one-pot base silylation/ nucleoside coupling procedure. The antiviral activities of all aza-nucleosides in vitro against a variety of vi

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