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1372798-59-8

6-chloro-3-(furan-2-carbonyl)-2-methylthio-4-phenylquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1372798-59-8 Structure

  • Basic information

    1. Product Name: 6-chloro-3-(furan-2-carbonyl)-2-methylthio-4-phenylquinoline
    2. Synonyms: 6-chloro-3-(furan-2-carbonyl)-2-methylthio-4-phenylquinoline
    3. CAS NO:1372798-59-8
    4. Molecular Formula:
    5. Molecular Weight: 379.867
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1372798-59-8.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: 6-chloro-3-(furan-2-carbonyl)-2-methylthio-4-phenylquinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-chloro-3-(furan-2-carbonyl)-2-methylthio-4-phenylquinoline(1372798-59-8)
    11. EPA Substance Registry System: 6-chloro-3-(furan-2-carbonyl)-2-methylthio-4-phenylquinoline(1372798-59-8)

  • 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: 1372798-59-8(Hazardous Substances Data)

1372798-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1372798-59-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,7,9 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1372798-59:
(9*1)+(8*3)+(7*7)+(6*2)+(5*7)+(4*9)+(3*8)+(2*5)+(1*9)=208
208 % 10 = 8
So 1372798-59-8 is a valid CAS Registry Number.

1372798-59-8Downstream Products

1372798-59-8Relevant articles and documents

InCl3-driven regioselective synthesis of functionalized/ annulated quinolines: Scope and limitations

Chanda, Tanmoy,Verma, Rajiv Kumar,Singh, Maya Shankar

supporting information; experimental part, p. 778 - 787 (2012/06/29)

The efficient, regioselective synthesis of functionalized/annulated quinolines was achieved by the coupling of 2-aminoaryl ketones with alkynes/active methylenes/α-oxoketene dithioacetals promoted by InCl 3 in refluxing acetonitrile as well as under solvent-free conditions in excellent yields. This transformation presumably proceeded through the hydroamination-hydroarylation of alkynes, and the Friedlaender annulation of active methylene compounds and α-oxoketene dithioacetals with 2-aminoarylketones. In addition, simple reductive and oxidative cyclization of 2-nitrobenzaldehyde and 2-aminobenzylalcohol, respectively, afforded substituted quinolines. Systematic optimization of the reaction parameters allowed us to identify two-component coupling (2CC) conditions that were tolerant of a wide range of functional groups, thereby providing densely functionalized/annulated quinolines. This approach tolerates the synthesis of various bioactive quinoline frameworks from the same 2-aminoarylketones under mild conditions, thus making this strategy highly useful in diversity-oriented synthesis (DOS). The scope and limitations of the alkyne-, activated methylene-, and α-oxoketene dithioacetal components on the reaction were also investigated.

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