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CAS

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524033-38-3

Piperazine, 1-(5-chloro-2-nitrophenyl)-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 524033-38-3 Structure

  • Basic information

    1. Product Name: Piperazine, 1-(5-chloro-2-nitrophenyl)-4-phenyl-
    2. Synonyms: 1-(5-CHLORO-2-NITROPHENYL)-4-PHENYLPIPERAZINE
    3. CAS NO:524033-38-3
    4. Molecular Formula: C16H16ClN3O2
    5. Molecular Weight: 317.77
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 524033-38-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Piperazine, 1-(5-chloro-2-nitrophenyl)-4-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Piperazine, 1-(5-chloro-2-nitrophenyl)-4-phenyl-(524033-38-3)
    11. EPA Substance Registry System: Piperazine, 1-(5-chloro-2-nitrophenyl)-4-phenyl-(524033-38-3)

  • 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: 524033-38-3(Hazardous Substances Data)

524033-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 524033-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,4,0,3 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 524033-38:
(8*5)+(7*2)+(6*4)+(5*0)+(4*3)+(3*3)+(2*3)+(1*8)=113
113 % 10 = 3
So 524033-38-3 is a valid CAS Registry Number.

524033-38-3Downstream Products

524033-38-3Relevant articles and documents

Specific features of nucleophilic substitution in 1-chloro-3,4- dinitrobenzene

Zotova,Kushakova,Kuznetsov,Rodin,Garabadzhiu

, p. 1473 - 1476 (2007/10/03)

Effects of the solvent, temperature, and nucleophile nature on the selectivity of nucleophilic substitution in 1-chloro-3,4-dinitrobenzene were studied, and optimal conditions were found for the synthesis and isolation of particular products.

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