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1027026-71-6

C21H22ClN3O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1027026-71-6 Structure

  • Basic information

    1. Product Name: C21H22ClN3O2
    2. Synonyms:
    3. CAS NO:1027026-71-6
    4. Molecular Formula:
    5. Molecular Weight: 383.878
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1027026-71-6.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: C21H22ClN3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H22ClN3O2(1027026-71-6)
    11. EPA Substance Registry System: C21H22ClN3O2(1027026-71-6)

  • 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: 1027026-71-6(Hazardous Substances Data)

1027026-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1027026-71-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,0,2 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1027026-71:
(9*1)+(8*0)+(7*2)+(6*7)+(5*0)+(4*2)+(3*6)+(2*7)+(1*1)=106
106 % 10 = 6
So 1027026-71-6 is a valid CAS Registry Number.

1027026-71-6Downstream Products

1027026-71-6Relevant articles and documents

Generation of 3,8-substituted 1,2,4-triazolopyridines as potent inhibitors of human 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1)

Wang, Haixia,Robl, Jeffrey A.,Hamann, Lawrence G.,Simpkins, Ligaya,Golla, Rajasree,Li, Yi-Xin,Seethala, Ramakrishna,Zvyaga, Tatyana,Gordon, David A.,Li, James J.

, p. 4146 - 4149 (2011/08/10)

A series of pyridyl amide/sulfonamide inhibitors of 11β-HSD-1 were modified to incorporate a novel 1,2,4-triazolopyridine scaffold. Optimization of substituents at the 3 and 8 position of the TZP core, with a special focus on enhancing metabolic stability, resulted in the identification of compound 38 as a potent and metabolically stable inhibitor of the enzyme.

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