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209268-82-6

6,13-DIHYDRO-5H-INDOLO[3,2-C]ACRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 209268-82-6 Structure

  • Basic information

    1. Product Name: 6,13-DIHYDRO-5H-INDOLO[3,2-C]ACRIDINE
    2. Synonyms: 6,13-DIHYDRO-5H-INDOLO[3,2-C]ACRIDINE;3,21-diazapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{15,20}]henicosa-1(21),2(10),4(9),5,7,13,15(20),16,18-nonaene
    3. CAS NO:209268-82-6
    4. Molecular Formula: C19H14N2
    5. Molecular Weight: 270.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 209268-82-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6,13-DIHYDRO-5H-INDOLO[3,2-C]ACRIDINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,13-DIHYDRO-5H-INDOLO[3,2-C]ACRIDINE(209268-82-6)
    11. EPA Substance Registry System: 6,13-DIHYDRO-5H-INDOLO[3,2-C]ACRIDINE(209268-82-6)

  • 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: 209268-82-6(Hazardous Substances Data)

209268-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209268-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,2,6 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 209268-82:
(8*2)+(7*0)+(6*9)+(5*2)+(4*6)+(3*8)+(2*8)+(1*2)=146
146 % 10 = 6
So 209268-82-6 is a valid CAS Registry Number.

209268-82-6Downstream Products

209268-82-6Relevant articles and documents

Preparation and Study of Tautomers Derived from 2-(2′-Pyridyl)indole and Related Compounds

Wu, Feiyue,Hardesty, Jon,Thummel, Randolph P.

, p. 4055 - 4061 (2007/10/03)

Methylation of 2-(2′-pyridyl)indole provides the corresponding N-methylated salt that undergoes deprotonation with mild base to provide the tautomeric (E)-1-methyl-2-(2′-indolenylidene)-l,2-dihydropyridine, whose geometry is established through a NOE expe

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