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CAS

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468078-24-2

N,N-diisopropyl-1-(tert-butyldiphenylsilyl)-1H-indole-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 468078-24-2 Structure

  • Basic information

    1. Product Name: N,N-diisopropyl-1-(tert-butyldiphenylsilyl)-1H-indole-3-carboxamide
    2. Synonyms: N,N-diisopropyl-1-(tert-butyldiphenylsilyl)-1H-indole-3-carboxamide
    3. CAS NO:468078-24-2
    4. Molecular Formula:
    5. Molecular Weight: 482.741
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 468078-24-2.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,N-diisopropyl-1-(tert-butyldiphenylsilyl)-1H-indole-3-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-diisopropyl-1-(tert-butyldiphenylsilyl)-1H-indole-3-carboxamide(468078-24-2)
    11. EPA Substance Registry System: N,N-diisopropyl-1-(tert-butyldiphenylsilyl)-1H-indole-3-carboxamide(468078-24-2)

  • 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: 468078-24-2(Hazardous Substances Data)

468078-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 468078-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,8,0,7 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 468078-24:
(8*4)+(7*6)+(6*8)+(5*0)+(4*7)+(3*8)+(2*2)+(1*4)=182
182 % 10 = 2
So 468078-24-2 is a valid CAS Registry Number.

468078-24-2Downstream Products

468078-24-2Relevant articles and documents

Preparation of 3,4-enynoindoles via directed lithiation and application to the synthesis of 3,4-carbocycloindoles

Pérez-Serrano, Leticia,Casarrubios, Luis,Domínguez, Gema,Freire, Guillermo,Pérez-Castells, Javier

, p. 5407 - 5415 (2002)

Lithiation at C4 of the indole nucleus is readily directed by several functional groups. The 4-substituted indoles thus obtained are transformed into suitable substrates for metathesis reactions. Ring-closing metathesis effected on these compounds lead to skeletons related to several indole alkaloids.

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