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CAS

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57240-61-6

N-ethyl-2,3-dimethylindole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 57240-61-6 Structure

  • Basic information

    1. Product Name: N-ethyl-2,3-dimethylindole
    2. Synonyms: N-ethyl-2,3-dimethylindole
    3. CAS NO:57240-61-6
    4. Molecular Formula:
    5. Molecular Weight: 173.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 57240-61-6.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-ethyl-2,3-dimethylindole(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-ethyl-2,3-dimethylindole(57240-61-6)
    11. EPA Substance Registry System: N-ethyl-2,3-dimethylindole(57240-61-6)

  • 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: 57240-61-6(Hazardous Substances Data)

57240-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57240-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,4 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57240-61:
(7*5)+(6*7)+(5*2)+(4*4)+(3*0)+(2*6)+(1*1)=116
116 % 10 = 6
So 57240-61-6 is a valid CAS Registry Number.

57240-61-6Downstream Products

57240-61-6Relevant articles and documents

Reactions of Electron-rich Heterocycles with Orthocarboxylic Acid Derivatives, 9. - Acylation of Indole and Methylindoles with Dialkoxycarbenium Tetrafluoroborates

Pindur, Ulf,Flo, Camran,Akguen, Eyuep,Tunali, Mustafa

, p. 1621 - 1627 (2007/10/02)

Indole and some methylindoles 1 were acylated regioselectively with dialkoxycarbenium tetrafluoroborates 2 under mild conditions.The formyl cation equivalent 2a' reacts with excess of indoles 1 to give the bisindolylcarbenium tetrafluoroborates 13a-d.

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