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CAS

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68289-71-4

2,3-dimethyl-6-methoxy-7-nitroindole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 68289-71-4 Structure

  • Basic information

    1. Product Name: 2,3-dimethyl-6-methoxy-7-nitroindole
    2. Synonyms:
    3. CAS NO:68289-71-4
    4. Molecular Formula:
    5. Molecular Weight: 220.228
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 68289-71-4.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: 2,3-dimethyl-6-methoxy-7-nitroindole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-dimethyl-6-methoxy-7-nitroindole(68289-71-4)
    11. EPA Substance Registry System: 2,3-dimethyl-6-methoxy-7-nitroindole(68289-71-4)

  • 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: 68289-71-4(Hazardous Substances Data)

68289-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68289-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,8 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 68289-71:
(7*6)+(6*8)+(5*2)+(4*8)+(3*9)+(2*7)+(1*1)=174
174 % 10 = 4
So 68289-71-4 is a valid CAS Registry Number.

68289-71-4Downstream Products

68289-71-4Relevant articles and documents

Synthesis of nitro- and aminoindoles

Yamashkin,Yurovskaya

, p. 1426 - 1432 (1999)

Optimal conditions are proposed for the direct nitration of 2,3-dimethylindoles containing methyl and methoxy groups in the benzene ring. In contrast to 5- and 6-methylindoles and 5- and 6-methoxyindoles, nitration of 7-methyl- and 7-methoxy-2,3-dimethylindoles proceeds differently under the same conditions. A series of previously unreported aminoindoles was obtained by reduction of the nitroindoles. 1999 Kluwer Academic/Plenum Publishers.

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