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2-Phenylcyclobutachinoxalin-1(3H)-on is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17398-22-0

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  • 17398-22-0 Structure
  • Basic information

    1. Product Name: 2-Phenylcyclobutachinoxalin-1(3H)-on
    2. Synonyms:
    3. CAS NO:17398-22-0
    4. Molecular Formula:
    5. Molecular Weight: 246.268
    6. EINECS: N/A
    7. Product Categories: N/A
  • 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-Phenylcyclobutachinoxalin-1(3H)-on(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Phenylcyclobutachinoxalin-1(3H)-on(17398-22-0)
    11. EPA Substance Registry System: 2-Phenylcyclobutachinoxalin-1(3H)-on(17398-22-0)
  • 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: 17398-22-0(Hazardous Substances Data)

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17398-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17398-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,9 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17398-22:
(7*1)+(6*7)+(5*3)+(4*9)+(3*8)+(2*2)+(1*2)=130
130 % 10 = 0
So 17398-22-0 is a valid CAS Registry Number.

17398-22-0Downstream Products

17398-22-0Relevant academic research and scientific papers

Preparation and Reactions of 3-Phenyl-4-pseudohalocyclobutenediones

Ried, Walter,Dietschmann, Hans

, p. 1003 - 1008 (2007/10/02)

3-Phenyl-4-pseudohalocyclobutenediones 2, 3 are prepared from 3-halo-4-phenylcyclobutenediones.The thio- and selenoethers 4 and the thio- and selenoureas 5 are obtained from 2 and 3 as secondary products.The reaction products of 2a and 3a with aromatic and heteroaromatic 1,2-diamines are described.Action of chlorine on 3a leads to the chloroformimidoyl chloride 9.On treatment with bases the four-membered ring of 2a is cleaved.

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