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1067645-72-0

C14H12N2O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1067645-72-0 Structure

  • Basic information

    1. Product Name: C14H12N2O
    2. Synonyms: C14H12N2O
    3. CAS NO:1067645-72-0
    4. Molecular Formula:
    5. Molecular Weight: 224.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1067645-72-0.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: C14H12N2O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H12N2O(1067645-72-0)
    11. EPA Substance Registry System: C14H12N2O(1067645-72-0)

  • 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: 1067645-72-0(Hazardous Substances Data)

1067645-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1067645-72-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,7,6,4 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1067645-72:
(9*1)+(8*0)+(7*6)+(6*7)+(5*6)+(4*4)+(3*5)+(2*7)+(1*2)=170
170 % 10 = 0
So 1067645-72-0 is a valid CAS Registry Number.

1067645-72-0Upstream product

1067645-72-0Downstream Products

1067645-72-0Relevant articles and documents

Copper-catalyzed mild and efficient entry to 1-substituted indazolones

Tanimori, Shinji,Ozaki, Yuka,Iesaki, Yasukazu,Kirihata, Mitsunori

, p. 1973 - 1976 (2008)

A variety of 1-alkyl- and aryl-substituted indazolones were synthesized easily starting from commercially available 2-halobenzoic acids and hydrazines via the copper-catalyzed intramolecular C-N bond formation of 2-halobenzohydrazides under mild conditions.

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