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1616894-10-0

C15H12ClN3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1616894-10-0 Structure

  • Basic information

    1. Product Name: C15H12ClN3
    2. Synonyms: C15H12ClN3
    3. CAS NO:1616894-10-0
    4. Molecular Formula:
    5. Molecular Weight: 269.733
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1616894-10-0.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: C15H12ClN3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H12ClN3(1616894-10-0)
    11. EPA Substance Registry System: C15H12ClN3(1616894-10-0)

  • 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: 1616894-10-0(Hazardous Substances Data)

1616894-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1616894-10-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,6,8,9 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1616894-10:
(9*1)+(8*6)+(7*1)+(6*6)+(5*8)+(4*9)+(3*4)+(2*1)+(1*0)=190
190 % 10 = 0
So 1616894-10-0 is a valid CAS Registry Number.

1616894-10-0Downstream Products

1616894-10-0Relevant articles and documents

Base-mediated reaction of vinyl bromides with aryl azides: One-pot synthesis of 1,5-disubstituted 1,2,3-triazoles

Wu, Luyong,Chen, Yuxue,Luo, Jianheng,Sun, Qi,Peng, Mingsheng,Lin, Qiang

, p. 3847 - 3850 (2014)

A one-pot base-mediated reaction of azides and β- or α-vinyl bromides has been reported. The effects of bases and solvents have been investigated in the process. A variety of 1,5-disubstituted triazoles were prepared in low to good yields. Further studies reveal that the corresponding alkynes were produced as intermediates via elimination reaction. Under the same reaction conditions, the reactions of alkyl alkynes with phenyl azide would give 1,5-disubstituted 1,2,3-triazoles.

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