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1352221-09-0

N-(6-chloropyridin-3-yl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1352221-09-0 Structure

  • Basic information

    1. Product Name: N-(6-chloropyridin-3-yl)benzenesulfonamide
    2. Synonyms: N-(6-chloropyridin-3-yl)benzenesulfonamide
    3. CAS NO:1352221-09-0
    4. Molecular Formula:
    5. Molecular Weight: 268.724
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1352221-09-0.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-(6-chloropyridin-3-yl)benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(6-chloropyridin-3-yl)benzenesulfonamide(1352221-09-0)
    11. EPA Substance Registry System: N-(6-chloropyridin-3-yl)benzenesulfonamide(1352221-09-0)

  • 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: 1352221-09-0(Hazardous Substances Data)

1352221-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1352221-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,2,2 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1352221-09:
(9*1)+(8*3)+(7*5)+(6*2)+(5*2)+(4*2)+(3*1)+(2*0)+(1*9)=110
110 % 10 = 0
So 1352221-09-0 is a valid CAS Registry Number.

1352221-09-0Downstream Products

1352221-09-0Relevant articles and documents

Sulfonamidation of Aryl and Heteroaryl Halides through Photosensitized Nickel Catalysis

Kim, Taehoon,McCarver, Stefan J.,Lee, Chulbom,MacMillan, David W. C.

, p. 3488 - 3492 (2018)

Herein we report a highly efficient method for nickel-catalyzed C?N bond formation between sulfonamides and aryl electrophiles. This technology provides generic access to a broad range of N-aryl and N-heteroaryl sulfonamide motifs, which are widely represented in drug discovery. Initial mechanistic studies suggest an energy-transfer mechanism wherein C?N bond reductive elimination occurs from a triplet excited NiII complex. Late-stage sulfonamidation in the synthesis of a pharmacologically relevant structure is also demonstrated.

Copper-catalyzed N-arylation of sulfonamides with aryl bromides under mild conditions

Wang, Xiang,Guram, Anil,Ronk, Michael,Milne, Jacqueline E.,Tedrow, Jason S.,Faul, Margaret M.

supporting information; experimental part, p. 7 - 10 (2012/01/06)

This Letter describes a copper catalyzed sulfonamide coupling reaction with aryl bromides to form N-aryl sulfonamides under mild conditions, including the first examples of Cu-catalyzed sulfonamide coupling at room temperature. The reaction protocol tolerates a broad range of substrates including a variety of primary and secondary sulfonamides and challenging heteroaryl bromides such as 2-bromothiazole.

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