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19177-35-6

2-phenyl-3-phenylaminoindole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 19177-35-6 Structure

  • Basic information

    1. Product Name: 2-phenyl-3-phenylaminoindole
    2. Synonyms: 2-phenyl-3-phenylaminoindole
    3. CAS NO:19177-35-6
    4. Molecular Formula:
    5. Molecular Weight: 284.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19177-35-6.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: 2-phenyl-3-phenylaminoindole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenyl-3-phenylaminoindole(19177-35-6)
    11. EPA Substance Registry System: 2-phenyl-3-phenylaminoindole(19177-35-6)

  • 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: 19177-35-6(Hazardous Substances Data)

19177-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19177-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,7 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19177-35:
(7*1)+(6*9)+(5*1)+(4*7)+(3*7)+(2*3)+(1*5)=126
126 % 10 = 6
So 19177-35-6 is a valid CAS Registry Number.

19177-35-6Relevant articles and documents

Experimental Evidence for an Electron-Transfer Mechanism in the Reaction between 2-Phenyl-3-(phenylimino)-3H-indole and Grignard Reagents: Application of the Marcus Theory

Eberson, Lennart,Greci, Lucedio

, p. 2135 - 2139 (2007/10/02)

2-Phenyl-3-(phenylimino)-3H-indole reacts with 5-hexenylmagnesium bromide to give products of 1,2- and 1,4-addition and reduction.For both addition modes, the products are mixtures of 5-hexenyl- and cyclopentylmethyl-substituted derivatives.Since the 5-hexenyl radical undergoes cyclization to the cyclopentylmethyl radical, the reaction is interpreted on the basis of an electron-transfer mechanism.This is also supported by estimates of electron-transfer rate constants according to the Marcus theory.

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