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N-formyl-2-(2,4,6-trimethylphenyl)-pyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80574-61-4 Structure
  • Basic information

    1. Product Name: N-formyl-2-(2,4,6-trimethylphenyl)-pyrrolidine
    2. Synonyms:
    3. CAS NO:80574-61-4
    4. Molecular Formula:
    5. Molecular Weight: 217.311
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80574-61-4.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: N-formyl-2-(2,4,6-trimethylphenyl)-pyrrolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-formyl-2-(2,4,6-trimethylphenyl)-pyrrolidine(80574-61-4)
    11. EPA Substance Registry System: N-formyl-2-(2,4,6-trimethylphenyl)-pyrrolidine(80574-61-4)
  • 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: 80574-61-4(Hazardous Substances Data)

80574-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80574-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,7 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80574-61:
(7*8)+(6*0)+(5*5)+(4*7)+(3*4)+(2*6)+(1*1)=134
134 % 10 = 4
So 80574-61-4 is a valid CAS Registry Number.

80574-61-4Downstream Products

80574-61-4Relevant articles and documents

Friedel-Crafts Reactions. IV. The Use of Cyclic N-Formyl-2-Methoxyamines in Electrophilic Amidoalkylation of Aromatic Compounds

Malmberg, Mats,Nyberg, Klas

, p. 411 - 418 (2007/10/02)

Aromatic compounds react with cyclic N-formyl-2-methoxyamines in proton or Lewis acid catalyzed reactions, yielding 2-aryl substituted nitrogen heterocyclic compounds.These products are easily converted to the corresponding N-H and N-CH3 derivatives by acid hydrolysis and LiAlH4 reduction, respectively.

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