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CAS

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1450812-84-6

C8H12Br2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1450812-84-6 Structure

  • Basic information

    1. Product Name: C8H12Br2
    2. Synonyms: C8H12Br2
    3. CAS NO:1450812-84-6
    4. Molecular Formula:
    5. Molecular Weight: 267.991
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1450812-84-6.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: C8H12Br2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C8H12Br2(1450812-84-6)
    11. EPA Substance Registry System: C8H12Br2(1450812-84-6)

  • 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: 1450812-84-6(Hazardous Substances Data)

1450812-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1450812-84-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,8,1 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1450812-84:
(9*1)+(8*4)+(7*5)+(6*0)+(5*8)+(4*1)+(3*2)+(2*8)+(1*4)=146
146 % 10 = 6
So 1450812-84-6 is a valid CAS Registry Number.

1450812-84-6Relevant articles and documents

Formation of enehydrazine intermediates through coupling of phenylhydrazines with vinyl halides: Entry into the Fischer indole synthesis

Zhan, Fuxu,Liang, Guangxin

, p. 1266 - 1269 (2013/03/13)

Cut to the chase: Direct formation of an enehydrazine, an intermediate in the classic Fischer indole synthesis, solves the regioselectivity problem associated with indolization. This approach not only achieves selective synthesis of indoles through proper selection of the vinyl halide, but also leads to quick construction of desoxyeseroline and esermethole, as well as the key structural motif in the Akuammiline alkaloid vincorine. Copyright

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