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(5-methyl-1H-indol-3-yl)(4-nitrophenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1571843-92-9 Structure
  • Basic information

    1. Product Name: (5-methyl-1H-indol-3-yl)(4-nitrophenyl)methanone
    2. Synonyms: (5-methyl-1H-indol-3-yl)(4-nitrophenyl)methanone
    3. CAS NO:1571843-92-9
    4. Molecular Formula:
    5. Molecular Weight: 280.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1571843-92-9.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: (5-methyl-1H-indol-3-yl)(4-nitrophenyl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5-methyl-1H-indol-3-yl)(4-nitrophenyl)methanone(1571843-92-9)
    11. EPA Substance Registry System: (5-methyl-1H-indol-3-yl)(4-nitrophenyl)methanone(1571843-92-9)
  • 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: 1571843-92-9(Hazardous Substances Data)

1571843-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1571843-92-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,1,8,4 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1571843-92:
(9*1)+(8*5)+(7*7)+(6*1)+(5*8)+(4*4)+(3*3)+(2*9)+(1*2)=189
189 % 10 = 9
So 1571843-92-9 is a valid CAS Registry Number.

1571843-92-9Downstream Products

1571843-92-9Relevant articles and documents

Copper-catalyzed decarboxylative C3-acylation of free (N-H) indoles with α-oxocarboxylic acids

Wang, Cuiping,Wang, Shaoyan,Li, Hua,Yan, Jingbo,Chi, Haijun,Chen, Xichao,Zhang, Zhiqiang

, p. 1721 - 1724 (2014)

An efficient Cu-catalyzed decarboxylative C3-acylation of free (N-H) indoles using α-oxocarboxylic acids as acylating agents has been developed. This method was compatible with a variety of functional groups and provided an attractive alternative access to 3-acylindoles in moderate to high yields.

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