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CAS

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925422-54-4

1-(toluene-4-sulfonyl)-5-[5-(4-trifluoromethylphenyl)-pent-4-ynyl]-1,2,3,4-tetrahydropyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 925422-54-4 Structure

  • Basic information

    1. Product Name: 1-(toluene-4-sulfonyl)-5-[5-(4-trifluoromethylphenyl)-pent-4-ynyl]-1,2,3,4-tetrahydropyridine
    2. Synonyms: 1-(toluene-4-sulfonyl)-5-[5-(4-trifluoromethylphenyl)-pent-4-ynyl]-1,2,3,4-tetrahydropyridine
    3. CAS NO:925422-54-4
    4. Molecular Formula:
    5. Molecular Weight: 447.521
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 925422-54-4.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-(toluene-4-sulfonyl)-5-[5-(4-trifluoromethylphenyl)-pent-4-ynyl]-1,2,3,4-tetrahydropyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(toluene-4-sulfonyl)-5-[5-(4-trifluoromethylphenyl)-pent-4-ynyl]-1,2,3,4-tetrahydropyridine(925422-54-4)
    11. EPA Substance Registry System: 1-(toluene-4-sulfonyl)-5-[5-(4-trifluoromethylphenyl)-pent-4-ynyl]-1,2,3,4-tetrahydropyridine(925422-54-4)

  • 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: 925422-54-4(Hazardous Substances Data)

925422-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 925422-54-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,4,2 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 925422-54:
(8*9)+(7*2)+(6*5)+(5*4)+(4*2)+(3*2)+(2*5)+(1*4)=164
164 % 10 = 4
So 925422-54-4 is a valid CAS Registry Number.

925422-54-4Downstream Products

925422-54-4Relevant articles and documents

Enamides and enesulfonamides as nucleophiles: Formation of complex ring systems through a platinum(II)-catalyzed addition/Friedel-Crafts pathway

Kozak, Jennifer A.,Dodd, Jennifer M.,Harrison, Tyler J.,Jardine, Katherine J.,Patrick, Brian O.,Dake, Gregory R.

supporting information; experimental part, p. 6929 - 6935 (2009/12/06)

(Chemical Equation Presented) Cyclic enamine derivatives (enesulfonamides and enamides) tethered to an 1-arylalkynyl fragment undergo a platinum(II)-catalyzed tandem alkyne addition/Friedel-Crafts ring closure to formnitrogen-containing polycyclic structures.Regioselectivity in the initial addition of the enesulfonamide or enamide nucleophile to the platinum(II)-alkyne complex is important. Electron-rich arenes and heterocycles led to the formation of products resulting from an initial 6-endo cyclization. Twenty-three examples of this process are presented.

Platinum(II)-catalyzed cyclizations forming quaternary carbon centers, using enesulfonamides, enecarbamates, or enamides as nucleophiles

Harrison, Tyler J.,Patrick, Brian O.,Dake, Gregory R.

, p. 367 - 370 (2007/10/03)

(Chemical Equation Presented) Cyclic enesulfonamides, enecarbamates, or enamides tethered to an alkyne cyclize readily with use of platinum(II) chloride. This reaction generates quaternary-substituted carbon centers within simple spiro-fused or more compl

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