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CAS

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158151-04-3

N-benzoyl-2-ene-2-piperidinyl trifluoromethanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 158151-04-3 Structure

  • Basic information

    1. Product Name: N-benzoyl-2-ene-2-piperidinyl trifluoromethanesulfonate
    2. Synonyms: N-benzoyl-2-ene-2-piperidinyl trifluoromethanesulfonate
    3. CAS NO:158151-04-3
    4. Molecular Formula:
    5. Molecular Weight: 335.304
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 158151-04-3.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: N-benzoyl-2-ene-2-piperidinyl trifluoromethanesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzoyl-2-ene-2-piperidinyl trifluoromethanesulfonate(158151-04-3)
    11. EPA Substance Registry System: N-benzoyl-2-ene-2-piperidinyl trifluoromethanesulfonate(158151-04-3)

  • 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: 158151-04-3(Hazardous Substances Data)

158151-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158151-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,1,5 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 158151-04:
(8*1)+(7*5)+(6*8)+(5*1)+(4*5)+(3*1)+(2*0)+(1*4)=123
123 % 10 = 3
So 158151-04-3 is a valid CAS Registry Number.

158151-04-3Downstream Products

158151-04-3Relevant articles and documents

Palladium-catalyzed coupling of heteroaromatic triflates with acetylene and its application for a dynemicin A intermediate

Okita, Takaaki,Isobe, Minoru

, p. 3737 - 3744 (1995)

An acetylene moiety was introduced to a carbonyl carbon of amide group via its triflate in the presence of palladium catalyst. The reaction proceeded smoothly under mild conditions. Utilizing this methodology, a model compound of dynemicin A bearing acety

Conversion of N-acyllactames into α-alkylated cyclic enamides via vinyl triflates

Tasushima, Kazunori,Hirade, Tetsuya,Hasegawa, Hirohiko,Murai, Akio

, p. 801 - 802 (2007/10/03)

N-acylated six- or seven- membered lactams were converted effectively into various α-alkylated cyclic enamides via their corresponding vinyl triflates.

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