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773148-44-0

(1R,7R)-(2-phenylsulfonyl)-8-oxabicyclo[5.1.0]oct-2-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 773148-44-0 Structure

  • Basic information

    1. Product Name: (1R,7R)-(2-phenylsulfonyl)-8-oxabicyclo[5.1.0]oct-2-ene
    2. Synonyms: (1R,7R)-(2-phenylsulfonyl)-8-oxabicyclo[5.1.0]oct-2-ene
    3. CAS NO:773148-44-0
    4. Molecular Formula:
    5. Molecular Weight: 250.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 773148-44-0.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: (1R,7R)-(2-phenylsulfonyl)-8-oxabicyclo[5.1.0]oct-2-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,7R)-(2-phenylsulfonyl)-8-oxabicyclo[5.1.0]oct-2-ene(773148-44-0)
    11. EPA Substance Registry System: (1R,7R)-(2-phenylsulfonyl)-8-oxabicyclo[5.1.0]oct-2-ene(773148-44-0)

  • 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: 773148-44-0(Hazardous Substances Data)

773148-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 773148-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,3,1,4 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 773148-44:
(8*7)+(7*7)+(6*3)+(5*1)+(4*4)+(3*8)+(2*4)+(1*4)=180
180 % 10 = 0
So 773148-44-0 is a valid CAS Registry Number.

773148-44-0Relevant articles and documents

Jacobsen protocols for large-scale epoxidation of cyclic dienyl sulfones: Application to the (+)-pretazettine core

Ebrahimian, G. Reza,Du Jourdin, Xavier Mollat,Fuchs, Philip L.

supporting information; experimental part, p. 2630 - 2633 (2012/07/17)

A Jacobsen epoxidation protocol using H2O2 as oxidant was designed for the large-scale preparation of various epoxy vinyl sulfones. A number of cocatalysts were screened, and pH control led to increased reaction rate, higher turnover

Improved and environmentally friendly large-scale preparation of cyclohexadienyl-, cycloheptadienyl sulfone and enantiopure epoxy cycloheptyl sulfones

Park, Taesik,Torres, Eduardo,Fuchs, Philip L.

, p. 1895 - 1900 (2007/10/03)

Kilogram-scale amounts of cycloheptadienyl phenylsulfone and cyclohexadienyl phenylsulfone were prepared by one operation in 5 stages with over 50% yield and requiring no purification. A practical and efficient method for the Jacobsen asymmetric epoxidati

Synthesis of enantiopure termini-differentiated heptane stereotriads. 1 Application to side chain-functionalized tetrahydrofurans of IKD-8344

Jiang, Wanlong,Lantrip, Douglas A.,Fuchs

, p. 2181 - 2184 (2007/10/03)

(equation presented) Enantiopure epoxy cycloheptenyl sulfones syn-7b and anti-7b are prepared in five high-yielding and stereospecific operations from 1,3-cycloheptadiene. These substrates serve as effective precursors for cis- and trans-substituted tetra

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