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1352966-03-0

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

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  • 1352966-03-0 Structure

  • Basic information

    1. Product Name: N-methyl-N-(4-methylphenyl)pyridine-2-sulfonamide
    2. Synonyms: N-methyl-N-(4-methylphenyl)pyridine-2-sulfonamide
    3. CAS NO:1352966-03-0
    4. Molecular Formula:
    5. Molecular Weight: 262.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1352966-03-0.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-methyl-N-(4-methylphenyl)pyridine-2-sulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-methyl-N-(4-methylphenyl)pyridine-2-sulfonamide(1352966-03-0)
    11. EPA Substance Registry System: N-methyl-N-(4-methylphenyl)pyridine-2-sulfonamide(1352966-03-0)

  • 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: 1352966-03-0(Hazardous Substances Data)

1352966-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1352966-03-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,9,6 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1352966-03:
(9*1)+(8*3)+(7*5)+(6*2)+(5*9)+(4*6)+(3*6)+(2*0)+(1*3)=170
170 % 10 = 0
So 1352966-03-0 is a valid CAS Registry Number.

1352966-03-0Relevant articles and documents

Nickel-Catalyzed Intramolecular Desulfitative C - N Coupling: A Synthesis of Aromatic Amines

Chen, Xuemeng,Jia, Xiuwen,Kramer, S?ren,Li, Yue,Lian, Zhong,Liu, Jiangjun,Sun, Haotian

, p. 5702 - 5711 (2020)

A nickel-catalyzed intramolecular C - N coupling reaction via SO2 extrusion is presented. The use of a catalytic amount of BPh3 allows the transformation to take place under much milder conditions (60 °C) than previously reported C - N coupling reactions by CO or CO2 extrusion (160-180 °C). In addition, this method displays good functional group tolerance and versatility, as it can be applied to the synthesis of dialkyl aryl amines, alkyl diaryl amines, and triaryl amines. The robustness of the desulfitative C - N coupling is demonstrated by three high-yielding gram-scale reactions.

PdII-catalyzed C-H olefination of N-(2-pyridyl)sulfonyl anilines and arylalkylamines

Garcia-Rubia, Alfonso,Urones, Beatriz,Gomez Arrayas, Ramon,Carretero, Juan C.

supporting information; experimental part, p. 10927 - 10931 (2012/01/04)

Flexible friend: The N-(2-pyridyl)sulfonyl group acts as a removable directing group in the PdII-catalyzed aryl C-H ortho alkenylation of N-alkyl aniline, benzylamine, and phenethylamine derivatives with electron-poor alkenes. The products were obtained in high yields (70-90 %) and with complete regiocontrol. The mild reductive N-sulfonyl removal enables the construction of a variety of nitrogen heterocycles. EWG=electron-withdrawing group.

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