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1221066-54-1

C12H10ClN3O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1221066-54-1 Structure

  • Basic information

    1. Product Name: C12H10ClN3O3
    2. Synonyms:
    3. CAS NO:1221066-54-1
    4. Molecular Formula:
    5. Molecular Weight: 279.683
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1221066-54-1.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: C12H10ClN3O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H10ClN3O3(1221066-54-1)
    11. EPA Substance Registry System: C12H10ClN3O3(1221066-54-1)

  • 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: 1221066-54-1(Hazardous Substances Data)

1221066-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1221066-54-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,0,6 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1221066-54:
(9*1)+(8*2)+(7*2)+(6*1)+(5*0)+(4*6)+(3*6)+(2*5)+(1*4)=101
101 % 10 = 1
So 1221066-54-1 is a valid CAS Registry Number.

1221066-54-1Relevant articles and documents

Novel 6-N-arylcarboxamidopyrazolo[4,3-d]pyrimidin-7-one derivatives as potential anti-cancer agents

Devegowda, Vani N.,Kim, Jung Hyun,Han, Ki-Cheol,Yang, Eun Gyeong,Choo, Hyunah,Pae, Ae Nim,Nam, Ghilsoo,Choi, Kyung Il

scheme or table, p. 1630 - 1633 (2010/06/19)

A novel series of 3,5,6-trisubstituted pyrazolo[4,3-d]pyrimidin-7-one derivatives, especially 6-N-arylcarboxamidopyrazolo[4,3-d]pyrimidin-7-ones were synthesized and evaluated for their in vitro anticancer activities against various human cancer cell line

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