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108349-86-6

8-chloro-1-methyl-1H-pyrido[2,3-b]indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108349-86-6 Structure

  • Basic information

    1. Product Name: 8-chloro-1-methyl-1H-pyrido[2,3-b]indole
    2. Synonyms: 8-chloro-1-methyl-1H-pyrido[2,3-b]indole
    3. CAS NO:108349-86-6
    4. Molecular Formula:
    5. Molecular Weight: 216.67
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108349-86-6.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: 8-chloro-1-methyl-1H-pyrido[2,3-b]indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-chloro-1-methyl-1H-pyrido[2,3-b]indole(108349-86-6)
    11. EPA Substance Registry System: 8-chloro-1-methyl-1H-pyrido[2,3-b]indole(108349-86-6)

  • 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: 108349-86-6(Hazardous Substances Data)

108349-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108349-86-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,4 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108349-86:
(8*1)+(7*0)+(6*8)+(5*3)+(4*4)+(3*9)+(2*8)+(1*6)=136
136 % 10 = 6
So 108349-86-6 is a valid CAS Registry Number.

108349-86-6Downstream Products

108349-86-6Relevant articles and documents

base effect in the auto-tandem palladium-catalyzed synthesis of amino-substituted 1-methyl-1H-α-carbolines

Yadav, Ashok K.,Verbeeck, Stefan,Hostyn, Steven,Franck, Philippe,Sergeyev, Sergey,Maes, Bert U. W.

, p. 1060 - 1063 (2013)

An auto-tandem Pd-catalyzed process consisting of an intramolecular direct arylation and an intermolecular Buchwald-Hartwig reaction for C-ring amino-substituted 1-methyl-1H-α-carboline synthesis has been developed. A mechanistic study of the direct arylation reaction revealed a rate effect of the inorganic base on the C-H activation step ( base effect ). The amines, reagents in the tandem protocol, appear to have a similar effect on the direct arylation.

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