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CAS

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320420-15-3

N-[2-OXO-2-(4-PHENYLPIPERAZINO)ETHYL]BENZENECARBOXAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 320420-15-3 Structure

  • Basic information

    1. Product Name: N-[2-OXO-2-(4-PHENYLPIPERAZINO)ETHYL]BENZENECARBOXAMIDE
    2. Synonyms: N-[2-OXO-2-(4-PHENYLPIPERAZINO)ETHYL]BENZENECARBOXAMIDE;N-[2-oxo-2-(4-phenylpiperazin-1-yl)ethyl]benzamide
    3. CAS NO:320420-15-3
    4. Molecular Formula: C19H21N3O2
    5. Molecular Weight: 323.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 320420-15-3.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: N-[2-OXO-2-(4-PHENYLPIPERAZINO)ETHYL]BENZENECARBOXAMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[2-OXO-2-(4-PHENYLPIPERAZINO)ETHYL]BENZENECARBOXAMIDE(320420-15-3)
    11. EPA Substance Registry System: N-[2-OXO-2-(4-PHENYLPIPERAZINO)ETHYL]BENZENECARBOXAMIDE(320420-15-3)

  • 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: 320420-15-3(Hazardous Substances Data)

320420-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 320420-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,4,2 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 320420-15:
(8*3)+(7*2)+(6*0)+(5*4)+(4*2)+(3*0)+(2*1)+(1*5)=73
73 % 10 = 3
So 320420-15-3 is a valid CAS Registry Number.

320420-15-3Downstream Products

320420-15-3Relevant articles and documents

A simple base-mediated amidation of aldehydes with azides

Kulkarni, Sameer S.,Hu, Xiangdong,Manetsch, Roman

supporting information, p. 1193 - 1195 (2013/03/13)

A practical and efficient amidation reaction involving aromatic aldehydes and various azides under mild conditions is described. A broad spectrum of functional groups was tolerated, and the amides were synthesized in moderate to excellent yields, presenting an attractive alternative to the currently available synthetic methods.

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