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1316844-22-0

ethyl 2-methyl-5-phenyl-1H-pyrrole-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1316844-22-0 Structure

  • Basic information

    1. Product Name: ethyl 2-methyl-5-phenyl-1H-pyrrole-1-carboxylate
    2. Synonyms: ethyl 2-methyl-5-phenyl-1H-pyrrole-1-carboxylate
    3. CAS NO:1316844-22-0
    4. Molecular Formula:
    5. Molecular Weight: 229.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1316844-22-0.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: ethyl 2-methyl-5-phenyl-1H-pyrrole-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-methyl-5-phenyl-1H-pyrrole-1-carboxylate(1316844-22-0)
    11. EPA Substance Registry System: ethyl 2-methyl-5-phenyl-1H-pyrrole-1-carboxylate(1316844-22-0)

  • 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: 1316844-22-0(Hazardous Substances Data)

1316844-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1316844-22-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,6,8,4 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1316844-22:
(9*1)+(8*3)+(7*1)+(6*6)+(5*8)+(4*4)+(3*4)+(2*2)+(1*2)=150
150 % 10 = 0
So 1316844-22-0 is a valid CAS Registry Number.

1316844-22-0Relevant articles and documents

Reaction of α-amido sulfones with functionalized nitrocompounds: A new two-step synthesis of N-alkoxycarbonyl-2,5-disubstituted pyrroles

Ballini, Roberto,Gabrielli, Serena,Palmieri, Alessandro,Petrini, Marino

, p. 43258 - 43261 (2014)

Reaction of α-amido sulfones with nitro ketals promoted by KF on alumina provides the corresponding adducts which, upon treatment with p-toluenesulfonic acid, generate the corresponding N-alkoxycarbonyl-2,5-disubstituted pyrroles. The latter transformation involves a cascade process including ketal cleavage, ring closure and final aromatization by nitrous acid elimination.

Iodonium salts are key intermediates in Pd-catalyzed acetoxylation of pyrroles

Lubriks, Dmitrijs,Sokolovs, Igors,Suna, Edgars

supporting information; experimental part, p. 4324 - 4327 (2011/10/05)

A mild, room-temperature Pd-catalyzed acetoxylation of pyrroles with phenyliodonium acetate is described. The acetoxylation was found to proceed via the initial formation of pyrrolyl(phenyl)iodonium acetates, which were converted to acetoxypyrroles in the presence of Pd(OAc)2. The acetoxylation could also be carried out as a one-pot sequential procedure without the isolation of the intermediate iodonium salts.

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