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CAS

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222403-54-5

ethyl 1-acetyl-4-methyl-5-phenylpyrrole-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 222403-54-5 Structure

  • Basic information

    1. Product Name: ethyl 1-acetyl-4-methyl-5-phenylpyrrole-3-carboxylate
    2. Synonyms:
    3. CAS NO:222403-54-5
    4. Molecular Formula:
    5. Molecular Weight: 271.316
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 222403-54-5.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: ethyl 1-acetyl-4-methyl-5-phenylpyrrole-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 1-acetyl-4-methyl-5-phenylpyrrole-3-carboxylate(222403-54-5)
    11. EPA Substance Registry System: ethyl 1-acetyl-4-methyl-5-phenylpyrrole-3-carboxylate(222403-54-5)

  • 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: 222403-54-5(Hazardous Substances Data)

222403-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 222403-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,4,0 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 222403-54:
(8*2)+(7*2)+(6*2)+(5*4)+(4*0)+(3*3)+(2*5)+(1*4)=85
85 % 10 = 5
So 222403-54-5 is a valid CAS Registry Number.

222403-54-5Relevant articles and documents

An unusual ring expansion from the Zav'yalov pyrrole synthesis: Formation of oxacino[2,3-c]pyrroles

Gabbutt, Christopher D.,Hepworth, John D.,Heron, B. Mark,Elsegood, Mark R. J.,Clegg, William

, p. 289 - 290 (1999)

Enamino acids 2 and 5 undergo a facile cyclisation to afford the pyrrole 3 and isoindole 6 ring systems; a novel two atom ring expansion ensues when derivatives 5b,d are subjected to the cyclisation conditions, resulting in the formation of the new oxacin

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