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6,6-diphenyl-3,5,6,6a-tetrahydro-2H-cyclobutapyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135735-37-4

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  • 135735-37-4 Structure
  • Basic information

    1. Product Name: 6,6-diphenyl-3,5,6,6a-tetrahydro-2H-cyclobutapyran
    2. Synonyms: 6,6-diphenyl-3,5,6,6a-tetrahydro-2H-cyclobutapyran
    3. CAS NO:135735-37-4
    4. Molecular Formula:
    5. Molecular Weight: 262.351
    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: 6,6-diphenyl-3,5,6,6a-tetrahydro-2H-cyclobutapyran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,6-diphenyl-3,5,6,6a-tetrahydro-2H-cyclobutapyran(135735-37-4)
    11. EPA Substance Registry System: 6,6-diphenyl-3,5,6,6a-tetrahydro-2H-cyclobutapyran(135735-37-4)
  • 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: 135735-37-4(Hazardous Substances Data)

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135735-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135735-37-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,3 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 135735-37:
(8*1)+(7*3)+(6*5)+(5*7)+(4*3)+(3*5)+(2*3)+(1*7)=134
134 % 10 = 4
So 135735-37-4 is a valid CAS Registry Number.

135735-37-4Downstream Products

135735-37-4Relevant academic research and scientific papers

1-Oxa-2,3-cyclohexadiene ("2H-isopyran"): A strained heterocyclic allene undergoing cycloaddition reactions with characteristic typo-, regio- and stereoselectivities

Ruzziconi, Renzo,Naruse, Yuji,Schlosser, Manfred

, p. 4603 - 4610 (1991)

1-Oxa-2,3-cyclohexadiene can be readily generated by treatment of 5-bromo-3,4-dihydro-2H-pyran with potassium tert-butoxide in the presence of "18-crown-6" and can be trapped with dienes or olefins. The remarkable regio- and stereoselectivities with which [4+2] and [2+2] adducts are formed suggests a concerted, non-radical cycloaddition mechanism.

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