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CAS

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1427798-08-0

N-[3-(tert-butyldimethylsilyl)prop-2-yn-1-yl]-4-methylbenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1427798-08-0 Structure

  • Basic information

    1. Product Name: N-[3-(tert-butyldimethylsilyl)prop-2-yn-1-yl]-4-methylbenzenesulfonamide
    2. Synonyms: N-[3-(tert-butyldimethylsilyl)prop-2-yn-1-yl]-4-methylbenzenesulfonamide
    3. CAS NO:1427798-08-0
    4. Molecular Formula:
    5. Molecular Weight: 323.532
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1427798-08-0.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: N-[3-(tert-butyldimethylsilyl)prop-2-yn-1-yl]-4-methylbenzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[3-(tert-butyldimethylsilyl)prop-2-yn-1-yl]-4-methylbenzenesulfonamide(1427798-08-0)
    11. EPA Substance Registry System: N-[3-(tert-butyldimethylsilyl)prop-2-yn-1-yl]-4-methylbenzenesulfonamide(1427798-08-0)

  • 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: 1427798-08-0(Hazardous Substances Data)

1427798-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427798-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,7,9 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1427798-08:
(9*1)+(8*4)+(7*2)+(6*7)+(5*7)+(4*9)+(3*8)+(2*0)+(1*8)=200
200 % 10 = 0
So 1427798-08-0 is a valid CAS Registry Number.

1427798-08-0Downstream Products

1427798-08-0Relevant articles and documents

Dual gold catalysis: A novel synthesis of bicyclic and tricyclic pyrroles from n -propargyl ynamides

Tokimizu, Yusuke,Wieteck, Marcel,Rudolph, Matthias,Oishi, Shinya,Fujii, Nobutaka,Hashmi, A. Stephen K.,Ohno, Hiroaki

, p. 604 - 607 (2015)

Various N-propargyl ynamides were converted to bicylic and tricyclic pyrroles by the use of a cationic dual-activation gold catalyst. This reaction starts with the nucleophilic addition of a gold acetylide onto an ynamide triple bond at the ?2-position of the nitrogen atom. Thus, gold vinylidene is formed, and then a second cyclization takes place. The formation of the gold vinylidene is indicated by the evidence that not only aryl ynamides but also alkyl ynamides undergo C-H activation in these reactions.

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