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26148-65-2

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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  • 26148-65-2 Structure

  • Basic information

    1. Product Name: 1-methyl-1H-pyrido[2,3-b]indole
    2. Synonyms: 1H-Pyrido[2,3-b]indole, 1-methyl-
    3. CAS NO:26148-65-2
    4. Molecular Formula: C12H10N2
    5. Molecular Weight: 182.2212
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26148-65-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 356.1°C at 760 mmHg
    3. Flash Point: 169.1°C
    4. Appearance: N/A
    5. Density: 1.17g/cm3
    6. Vapor Pressure: 3E-05mmHg at 25°C
    7. Refractive Index: 1.658
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-methyl-1H-pyrido[2,3-b]indole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-methyl-1H-pyrido[2,3-b]indole(26148-65-2)
    12. EPA Substance Registry System: 1-methyl-1H-pyrido[2,3-b]indole(26148-65-2)

  • 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: 26148-65-2(Hazardous Substances Data)

26148-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26148-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,4 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26148-65:
(7*2)+(6*6)+(5*1)+(4*4)+(3*8)+(2*6)+(1*5)=112
112 % 10 = 2
So 26148-65-2 is a valid CAS Registry Number.

26148-65-2Relevant 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.

supporting information, p. 1060 - 1063 (2013/04/10)

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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