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1318801-00-1

C21H21ClFN3O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1318801-00-1 Structure

  • Basic information

    1. Product Name: C21H21ClFN3O
    2. Synonyms:
    3. CAS NO:1318801-00-1
    4. Molecular Formula:
    5. Molecular Weight: 385.869
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1318801-00-1.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: C21H21ClFN3O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H21ClFN3O(1318801-00-1)
    11. EPA Substance Registry System: C21H21ClFN3O(1318801-00-1)

  • 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: 1318801-00-1(Hazardous Substances Data)

1318801-00-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1318801-00-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,8,8,0 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1318801-00:
(9*1)+(8*3)+(7*1)+(6*8)+(5*8)+(4*0)+(3*1)+(2*0)+(1*0)=131
131 % 10 = 1
So 1318801-00-1 is a valid CAS Registry Number.

1318801-00-1Downstream Products

1318801-00-1Relevant 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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