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254964-20-0

(1R,4S)-N-(p-toluenesulfonyl)-2-vinylidene-7-azabicyclo[2.2.1]heptane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 254964-20-0 Structure

  • Basic information

    1. Product Name: (1R,4S)-N-(p-toluenesulfonyl)-2-vinylidene-7-azabicyclo[2.2.1]heptane
    2. Synonyms: (1R,4S)-N-(p-toluenesulfonyl)-2-vinylidene-7-azabicyclo[2.2.1]heptane
    3. CAS NO:254964-20-0
    4. Molecular Formula:
    5. Molecular Weight: 275.371
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 254964-20-0.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,4S)-N-(p-toluenesulfonyl)-2-vinylidene-7-azabicyclo[2.2.1]heptane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,4S)-N-(p-toluenesulfonyl)-2-vinylidene-7-azabicyclo[2.2.1]heptane(254964-20-0)
    11. EPA Substance Registry System: (1R,4S)-N-(p-toluenesulfonyl)-2-vinylidene-7-azabicyclo[2.2.1]heptane(254964-20-0)

  • 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: 254964-20-0(Hazardous Substances Data)

254964-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 254964-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,4,9,6 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 254964-20:
(8*2)+(7*5)+(6*4)+(5*9)+(4*6)+(3*4)+(2*2)+(1*0)=160
160 % 10 = 0
So 254964-20-0 is a valid CAS Registry Number.

254964-20-0Downstream Products

254964-20-0Relevant articles and documents

Application of an organozinc reagent derived from (S)-pyroglutamic acid: A formal synthesis of epibatidine

Karstens, Willem F. J.,Moolenaar, Marinus J.,Rutjes, Floris P. J. T.,Grabowska, Urszula,Speckamp, W. Nico,Hiemstra, Henk

, p. 8629 - 8632 (2007/10/03)

A formal total synthesis of natural (-)-epibatidine has been developed. Key steps in the synthesis are a copper(I)-mediated coupling of an (S)-pyroglutamic acid-derived organozinc reagent with 1-iodo-3-trimethylsilyl-1-propyne and an N-acyl- or N-sulfonyl

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