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77978-07-5

3-(1-tosylethyl)-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 77978-07-5 Structure

  • Basic information

    1. Product Name: 3-(1-tosylethyl)-1H-indole
    2. Synonyms:
    3. CAS NO:77978-07-5
    4. Molecular Formula:
    5. Molecular Weight: 299.393
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 77978-07-5.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: 3-(1-tosylethyl)-1H-indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(1-tosylethyl)-1H-indole(77978-07-5)
    11. EPA Substance Registry System: 3-(1-tosylethyl)-1H-indole(77978-07-5)

  • 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: 77978-07-5(Hazardous Substances Data)

77978-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77978-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,9,7 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77978-07:
(7*7)+(6*7)+(5*9)+(4*7)+(3*8)+(2*0)+(1*7)=195
195 % 10 = 5
So 77978-07-5 is a valid CAS Registry Number.

77978-07-5Relevant articles and documents

Copper-Catalyzed Addition of Grignard Reagents to in situ Generated Indole-Derived Vinylogous Imines

Ge, Luo,Harutyunyan, Syuzanna R.,Zurro, Mercedes

, p. 16277 - 16280 (2020/11/30)

Chiral indole derivatives are ubiquitous motifs in pharmaceuticals and alkaloids. Herein, the first protocol for catalytic asymmetric conjugate addition of Grignard reagents to various sulfonyl indoles, offering a straightforward approach for the synthesis of chiral 3-sec-alkyl-substituted indoles in high yields and enantiomeric ratios is presented. This methodology makes use of a chiral catalyst based on copper phosphoramidite complexes and in situ formation of vinylogous imine intermediates.

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