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CAS

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78710-70-0

1-(phenylsulfonyl)-trans-3,4-epoxypentane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78710-70-0 Structure

  • Basic information

    1. Product Name: 1-(phenylsulfonyl)-trans-3,4-epoxypentane
    2. Synonyms:
    3. CAS NO:78710-70-0
    4. Molecular Formula:
    5. Molecular Weight: 226.296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78710-70-0.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: 1-(phenylsulfonyl)-trans-3,4-epoxypentane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(phenylsulfonyl)-trans-3,4-epoxypentane(78710-70-0)
    11. EPA Substance Registry System: 1-(phenylsulfonyl)-trans-3,4-epoxypentane(78710-70-0)

  • 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: 78710-70-0(Hazardous Substances Data)

78710-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78710-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,1 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78710-70:
(7*7)+(6*8)+(5*7)+(4*1)+(3*0)+(2*7)+(1*0)=150
150 % 10 = 0
So 78710-70-0 is a valid CAS Registry Number.

78710-70-0Relevant articles and documents

Stereochemistry of Addition of Organocopper Reagents and of the Hydride Ion to 1-(Arylsulfonyl)bicyclobutanes

Gaoni, Yehiel,Tomazic, Alenka,Potgieter, Eleonora

, p. 2943 - 2947 (1985)

Addition of methylmagnesium iodide/cuprous iodide or of lithium dimethylcuprate to 2-exo- and 2-endo-methyl-1-(phenylsulfonyl)bicyclobutane and determination of the relative geometry of the methyls in the 2,3-dimethylcyclobutanes obtained allowed u

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