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CAS

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1198214-09-3

2-(1-methyl-1H-indol-3-yl)-1,4-diphenylbutane-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1198214-09-3 Structure

  • Basic information

    1. Product Name: 2-(1-methyl-1H-indol-3-yl)-1,4-diphenylbutane-1,4-dione
    2. Synonyms: 2-(1-methyl-1H-indol-3-yl)-1,4-diphenylbutane-1,4-dione
    3. CAS NO:1198214-09-3
    4. Molecular Formula:
    5. Molecular Weight: 367.447
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1198214-09-3.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: 2-(1-methyl-1H-indol-3-yl)-1,4-diphenylbutane-1,4-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1-methyl-1H-indol-3-yl)-1,4-diphenylbutane-1,4-dione(1198214-09-3)
    11. EPA Substance Registry System: 2-(1-methyl-1H-indol-3-yl)-1,4-diphenylbutane-1,4-dione(1198214-09-3)

  • 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: 1198214-09-3(Hazardous Substances Data)

1198214-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198214-09-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,2,1 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1198214-09:
(9*1)+(8*1)+(7*9)+(6*8)+(5*2)+(4*1)+(3*4)+(2*0)+(1*9)=163
163 % 10 = 3
So 1198214-09-3 is a valid CAS Registry Number.

1198214-09-3Downstream Products

1198214-09-3Relevant articles and documents

Ruthenium-catalyzed direct C3 alkylation of indoles with α,β-unsaturated ketones

Li, Shuai-Shuai,Lin, Hui,Zhang, Xiao-Mei,Dong, Lin

, p. 1254 - 1263 (2015)

In this paper, a simple and highly efficient ruthenium-catalyzed direct C3 alkylation of indoles with various α,β-unsaturated ketones without chelation assistance has been developed. This novel C-H activation methodology exhibits a broad substrate scope s

Indirect regioselective heteroarylation of indoles through a Friedel-Crafts reaction with (E)-1,4-diaryl-2-buten-1,4-diones

Blay, Gonzalo,Fernández, Isabel,Monleón, Alicia,Pedro, José R.,Vila, Carlos

experimental part, p. 9264 - 9270 (2010/01/06)

A two-step synthesis of 3-heteroaryl indoles has been developed. The first step of the sequence involves a Friedel-Crafts alkylation of indoles with 1,4-diaryl-2-buten-1,4-diones to give the corresponding indoles bearing a 1,4-dicarbonyl moiety. The reaction is catalyzed by InCl3 and takes place with good yields. Cyclization of the diones under different Paal-Knorr conditions allows to prepare indoles substituted at the C3 position with 3-furanyl, 3-pyrrolyl- and 3-thienyl moieties.

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