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174002-15-4

C8Cl2N2O2*C11H12N2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 174002-15-4 Structure

  • Basic information

    1. Product Name: C8Cl2N2O2*C11H12N2O
    2. Synonyms:
    3. CAS NO:174002-15-4
    4. Molecular Formula:
    5. Molecular Weight: 415.235
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 174002-15-4.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: C8Cl2N2O2*C11H12N2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C8Cl2N2O2*C11H12N2O(174002-15-4)
    11. EPA Substance Registry System: C8Cl2N2O2*C11H12N2O(174002-15-4)

  • 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: 174002-15-4(Hazardous Substances Data)

174002-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174002-15-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,0,0 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 174002-15:
(8*1)+(7*7)+(6*4)+(5*0)+(4*0)+(3*2)+(2*1)+(1*5)=94
94 % 10 = 4
So 174002-15-4 is a valid CAS Registry Number.

174002-15-4Downstream Products

174002-15-4Relevant articles and documents

Kinetic and thermodynamic studies on molecular interaction of antipyrine donor and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone as an electron acceptor in different solvents

Hasani, Masoumeh,Nikoee, Sheler

, p. 81 - 91 (2013)

The charge-transfer (CT) complex of donor antipyrine with I-acceptor 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) has been investigated spectrophotometrically in different halocarbon and acetonitrile solvents. The results indicated immediate formation

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