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N-(2-cyanophenyl)-4-fluorobenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 333442-22-1 Structure
  • Basic information

    1. Product Name: N-(2-cyanophenyl)-4-fluorobenzenesulfonamide
    2. Synonyms: N-(2-cyanophenyl)-4-fluorobenzenesulfonamide
    3. CAS NO:333442-22-1
    4. Molecular Formula: C13H9FN2O2S
    5. Molecular Weight: 276.2861632
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 333442-22-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2-cyanophenyl)-4-fluorobenzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-cyanophenyl)-4-fluorobenzenesulfonamide(333442-22-1)
    11. EPA Substance Registry System: N-(2-cyanophenyl)-4-fluorobenzenesulfonamide(333442-22-1)
  • 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: 333442-22-1(Hazardous Substances Data)

333442-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 333442-22-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,4,4 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 333442-22:
(8*3)+(7*3)+(6*3)+(5*4)+(4*4)+(3*2)+(2*2)+(1*2)=111
111 % 10 = 1
So 333442-22-1 is a valid CAS Registry Number.

333442-22-1Downstream Products

333442-22-1Relevant articles and documents

Nickel-Catalyzed β-Regioselective Amination/Cyclization of Ynamide-Nitriles with Amines: Synthesis of Functionalized 3-Aminoindoles and 4-Aminoisoquinolines

Hu, Xiaoping,Xie, Xin,Gan, Yi,Wang, Gaonan,Liu, Yuanhong

, p. 1296 - 1301 (2021)

A highly regioselective nickel/Lewis acid catalyzed amination/cyclization of ynamide-nitriles with amines involving β-addition has been developed. The reaction offers an attractive and efficient route for the synthesis of 3-aminoindoles and 4-aminoisoquinoline derivatives. The Ts-group on the ynamide acts as a directing group to produce the alkenyl nickel species with high regioselectivity.

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