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CAS

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736922-16-0

2'-fluoro-5'-nitro-2-[2-(1,2,3,4-tetrahydroisoquinolinolyl)]acetanilide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 736922-16-0 Structure

  • Basic information

    1. Product Name: 2'-fluoro-5'-nitro-2-[2-(1,2,3,4-tetrahydroisoquinolinolyl)]acetanilide
    2. Synonyms:
    3. CAS NO:736922-16-0
    4. Molecular Formula:
    5. Molecular Weight: 329.331
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 736922-16-0.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: 2'-fluoro-5'-nitro-2-[2-(1,2,3,4-tetrahydroisoquinolinolyl)]acetanilide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2'-fluoro-5'-nitro-2-[2-(1,2,3,4-tetrahydroisoquinolinolyl)]acetanilide(736922-16-0)
    11. EPA Substance Registry System: 2'-fluoro-5'-nitro-2-[2-(1,2,3,4-tetrahydroisoquinolinolyl)]acetanilide(736922-16-0)

  • 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: 736922-16-0(Hazardous Substances Data)

736922-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 736922-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,6,9,2 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 736922-16:
(8*7)+(7*3)+(6*6)+(5*9)+(4*2)+(3*2)+(2*1)+(1*6)=180
180 % 10 = 0
So 736922-16-0 is a valid CAS Registry Number.

736922-16-0Downstream Products

736922-16-0Relevant articles and documents

Synthesis of quinoxaline derivatives from substituted acetanilides through intramolecular quaternization reactions

De Castro, Sonia,Chicharro, Roberto,Aran, Vicente J.

, p. 790 - 802 (2007/10/03)

The cyclization of 2-dialkylamino-2′-halogeno- and 2-chloro-2′-(dialkylamino)acetanilides to quinoxaline derivatives has been studied in detail. These reactions proceed, respectively, through intramolecular aromatic nucleophilic or aliphatic nucleophilic

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