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1006867-19-1

C20H25F4N3O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1006867-19-1 Structure

  • Basic information

    1. Product Name: C20H25F4N3O3
    2. Synonyms: C20H25F4N3O3
    3. CAS NO:1006867-19-1
    4. Molecular Formula:
    5. Molecular Weight: 431.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1006867-19-1.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: C20H25F4N3O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H25F4N3O3(1006867-19-1)
    11. EPA Substance Registry System: C20H25F4N3O3(1006867-19-1)

  • 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: 1006867-19-1(Hazardous Substances Data)

1006867-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1006867-19-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,8,6 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1006867-19:
(9*1)+(8*0)+(7*0)+(6*6)+(5*8)+(4*6)+(3*7)+(2*1)+(1*9)=141
141 % 10 = 1
So 1006867-19-1 is a valid CAS Registry Number.

1006867-19-1Downstream Products

1006867-19-1Relevant articles and documents

Development of CXCR3 antagonists. Part 3: Tropenyl and homotropenyl-piperidine urea derivatives

Watson, Robert J.,Allen, Daniel R.,Birch, Helen L.,Chapman, Gayle A.,Galvin, Frances C.,Jopling, Louise A.,Knight, Roland L.,Meier, Dorica,Oliver, Kathryn,Meissner, Johannes W.G.,Owen, David A.,Thomas, Elizabeth J.,Tremayne, Neil,Williams, Sophie C.

, p. 147 - 151 (2008/09/17)

The optimization of a series of 1-aryl-3-piperidinyl urea derivatives is described in which incorporation of tropenyl and homotropenyl moieties has led to significant improvements in activity and drug-like properties. Replacement of the central piperidine

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