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CAS

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83670-37-5

acetic acid-(2,4,6-tribromo-N-methyl-anilide) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83670-37-5 Structure

  • Basic information

    1. Product Name: acetic acid-(2,4,6-tribromo-N-methyl-anilide)
    2. Synonyms:
    3. CAS NO:83670-37-5
    4. Molecular Formula:
    5. Molecular Weight: 385.881
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83670-37-5.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: acetic acid-(2,4,6-tribromo-N-methyl-anilide)(CAS DataBase Reference)
    10. NIST Chemistry Reference: acetic acid-(2,4,6-tribromo-N-methyl-anilide)(83670-37-5)
    11. EPA Substance Registry System: acetic acid-(2,4,6-tribromo-N-methyl-anilide)(83670-37-5)

  • 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: 83670-37-5(Hazardous Substances Data)

83670-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83670-37-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,7 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83670-37:
(7*8)+(6*3)+(5*6)+(4*7)+(3*0)+(2*3)+(1*7)=145
145 % 10 = 5
So 83670-37-5 is a valid CAS Registry Number.

83670-37-5Downstream Products

83670-37-5Relevant articles and documents

Novel Bromination Reagents. Electrophilic Aromatic Bromination by Hexabromocyclopentadiene

Fuchs, Benzion,Belsky, Yigal,Tartakovsky, Evgeny,Zizuashvili, Jakob,Weinman, Sarah

, p. 778 - 779 (1982)

Hexabromocyclopentadiene efficiently and regioselectively brominates activated aromatic compounds, in a process which is interpreted as involving ready formation of the pentabromocyclopentadienide anion by bromonium ion release.

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