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CAS

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123767-92-0

1-(4-bromophenylamino)-2-nitro-3-(4-bromophenylimino)propene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123767-92-0 Structure

  • Basic information

    1. Product Name: 1-(4-bromophenylamino)-2-nitro-3-(4-bromophenylimino)propene
    2. Synonyms:
    3. CAS NO:123767-92-0
    4. Molecular Formula:
    5. Molecular Weight: 425.079
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123767-92-0.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: 1-(4-bromophenylamino)-2-nitro-3-(4-bromophenylimino)propene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-bromophenylamino)-2-nitro-3-(4-bromophenylimino)propene(123767-92-0)
    11. EPA Substance Registry System: 1-(4-bromophenylamino)-2-nitro-3-(4-bromophenylimino)propene(123767-92-0)

  • 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: 123767-92-0(Hazardous Substances Data)

123767-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123767-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,7,6 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123767-92:
(8*1)+(7*2)+(6*3)+(5*7)+(4*6)+(3*7)+(2*9)+(1*2)=140
140 % 10 = 0
So 123767-92-0 is a valid CAS Registry Number.

123767-92-0Downstream Products

123767-92-0Relevant articles and documents

NITROAZINES. XIV. AMBIDENT NATURE OF ARYLAMINES IN REACTIONS WITH 6-NITROAZOLOPYRIMIDINES

Rusinov, V. L.,Tumashov, A. A.,Pilicheva, T. L.,Chupakhin, O. N.

, p. 952 - 957 (2007/10/02)

During the reaction of 6-nitroazolopyrimidines with dialkylanilines the products from addition at the carbon atom, i.e., 6-nitro-7-p-dialkylaminophenyl-4,7-dihydroazolopyrimidines are formed.The reaction with aniline and its derivatives leads to destruction of the pyrimidine ring as a result of N-addition of the arylamine.

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