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CAS

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193072-49-0

1-Pentanone, 1-(4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)-4-nitro-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 193072-49-0 Structure

  • Basic information

    1. Product Name: 1-Pentanone, 1-(4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)-4-nitro-3-phenyl-
    2. Synonyms:
    3. CAS NO:193072-49-0
    4. Molecular Formula: C33H30N2O5
    5. Molecular Weight: 534.612
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 193072-49-0.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: 1-Pentanone, 1-(4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)-4-nitro-3-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Pentanone, 1-(4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)-4-nitro-3-phenyl-(193072-49-0)
    11. EPA Substance Registry System: 1-Pentanone, 1-(4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)-4-nitro-3-phenyl-(193072-49-0)

  • 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: 193072-49-0(Hazardous Substances Data)

193072-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193072-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,0,7 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 193072-49:
(8*1)+(7*9)+(6*3)+(5*0)+(4*7)+(3*2)+(2*4)+(1*9)=140
140 % 10 = 0
So 193072-49-0 is a valid CAS Registry Number.

193072-49-0Downstream Products

193072-49-0Relevant articles and documents

Synthesis of some indolylpyrroles and indolylpyrrolylketones

Black, David StC.,Bowyer, Michael C.,Kumar, Naresh

, p. 8565 - 8572 (1997)

The 2-(7-indolyl)pyrrole 12 has been synthesised from 4,6-dimethoxy-2,3-diphenylindole 4 via the 1,4-diketone 11, generated from the 4-nitroketone 7. Reaction of tosylmethylisocyanide with some α,β-unsaturated ketones also yielded the indolylpyrrole 15 and the indolylpyrrolylkelones 13 and 17.

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