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1198613-05-6

C16H14BrN3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1198613-05-6 Structure

  • Basic information

    1. Product Name: C16H14BrN3
    2. Synonyms: C16H14BrN3
    3. CAS NO:1198613-05-6
    4. Molecular Formula:
    5. Molecular Weight: 328.211
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1198613-05-6.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: C16H14BrN3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H14BrN3(1198613-05-6)
    11. EPA Substance Registry System: C16H14BrN3(1198613-05-6)

  • 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: 1198613-05-6(Hazardous Substances Data)

1198613-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198613-05-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,6,1 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1198613-05:
(9*1)+(8*1)+(7*9)+(6*8)+(5*6)+(4*1)+(3*3)+(2*0)+(1*5)=176
176 % 10 = 6
So 1198613-05-6 is a valid CAS Registry Number.

1198613-05-6Downstream Products

1198613-05-6Relevant articles and documents

Bromo-directed N-2 alkylation of NH-1,2,3-triazoles: Efficient synthesis of poly-substituted 1,2,3-triazoles

Wang, Xiao-Jun,Sidhu, Kanwar,Zhang, Li,Campbell, Scot,Haddad, Nizar,Reeves, Diana C.,Krishnamurthy, Dhileepkumar,Senanayake, Chris H.

supporting information; experimental part, p. 5490 - 5493 (2010/02/28)

"Chemical Equation Presented" Reaction of 4-bromo-NH-1,2,3- triazoles 2 with alkyl halides In the presence of K2CO3 in DMF produced the corresponding 2-substituted 4-bromo1,2,3-triazoles 5 In a regioselective process. Subsequent Suzuki cross-coupling reaction of these bromides provided an efficient synthesis of 2,4,5-trisubstituted triazoles 3. In addition, reduction of the bromotriazoles by hydrogenation furnished an efficient synthesis of 2,4-disubstituted triazoles 8.

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