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430432-26-1

N-(2-chloro-phenethyl)-toluene-4-sulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 430432-26-1 Structure

  • Basic information

    1. Product Name: N-(2-chloro-phenethyl)-toluene-4-sulfonamide
    2. Synonyms: N-(2-chloro-phenethyl)-toluene-4-sulfonamide
    3. CAS NO:430432-26-1
    4. Molecular Formula:
    5. Molecular Weight: 309.817
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 430432-26-1.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-(2-chloro-phenethyl)-toluene-4-sulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-chloro-phenethyl)-toluene-4-sulfonamide(430432-26-1)
    11. EPA Substance Registry System: N-(2-chloro-phenethyl)-toluene-4-sulfonamide(430432-26-1)

  • 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: 430432-26-1(Hazardous Substances Data)

430432-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 430432-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,0,4,3 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 430432-26:
(8*4)+(7*3)+(6*0)+(5*4)+(4*3)+(3*2)+(2*2)+(1*6)=101
101 % 10 = 1
So 430432-26-1 is a valid CAS Registry Number.

430432-26-1Downstream Products

430432-26-1Relevant articles and documents

Electrochemical C?H Amidation of Heteroarenes with N-Alkyl Sulfonamides in Aqueous Medium

Zhang, Yan,Lin, Zhipeng,Ackermann, Lutz

, p. 242 - 246 (2021)

The construction of C?N bonds by free radical reactions represents a powerful synthetic approach for direct C?H amidations of arenes or heteroarenes. Developing efficient and more environmentally friendly synthetic methods for C?H amidation reactions remains highly desirable. Herein, metal-free electrochemical oxidative dehydrogenative C?H amidations of heteroarenes with N-alkylsulfonamides have been accomplished. The catalyst- and chemical-oxidant-free C?H amidation features an ample scope and employs electricity as the green and sole oxidant. A variety of heteroarenes, including indoles, pyrroles, benzofuran and benzothiophene, thereby underwent this C(sp2)?H nitrogenation. Cyclic voltammetry studies and control experiments provided evidence for nitrogen-centered radicals being directly generated under metal-free electrocatalysis.

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