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4,5-diphenyl-<6H>-cyclopenta--thiophen-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73340-39-3

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  • 73340-39-3 Structure
  • Basic information

    1. Product Name: 4,5-diphenyl-<6H>-cyclopenta--thiophen-6-one
    2. Synonyms:
    3. CAS NO:73340-39-3
    4. Molecular Formula:
    5. Molecular Weight: 288.37
    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: 4,5-diphenyl-<6H>-cyclopenta--thiophen-6-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,5-diphenyl-<6H>-cyclopenta--thiophen-6-one(73340-39-3)
    11. EPA Substance Registry System: 4,5-diphenyl-<6H>-cyclopenta--thiophen-6-one(73340-39-3)
  • 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: 73340-39-3(Hazardous Substances Data)

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73340-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73340-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,4 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73340-39:
(7*7)+(6*3)+(5*3)+(4*4)+(3*0)+(2*3)+(1*9)=113
113 % 10 = 3
So 73340-39-3 is a valid CAS Registry Number.

73340-39-3Downstream Products

73340-39-3Relevant academic research and scientific papers

The reaction of (η5-cyclopentadienyl)dicarbonyliron(2-thienoyl) with acetylenes; a mechanistic study using proton nuclear magnetic resonance, and application in synthesis

Butler, Ian R.

, p. 1979 - 1987 (2007/10/02)

The thermal reaction of dicarbonyl-η5-cyclopentadienyl(2-thienoyl)iron with a series of substituted acetylenes to give indenones and cyclopentathiophenones have been reinvestigated.The results obtained support a reaction mechanism involving initial acetylene insertion followed by that of carbon monoxide, in contradiction to the previously reported results.The reaction products were identified and characterized primarily using 2D 1H nmr spectroscopy.

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