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86296-94-8

1-Acetyl-3-cyano-5-methyl-2,4-diphenyl-2,3-dihydro-1H-pyrrole-3-carboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86296-94-8 Structure

  • Basic information

    1. Product Name: 1-Acetyl-3-cyano-5-methyl-2,4-diphenyl-2,3-dihydro-1H-pyrrole-3-carboxylic acid methyl ester
    2. Synonyms: 1-Acetyl-3-cyano-5-methyl-2,4-diphenyl-2,3-dihydro-1H-pyrrole-3-carboxylic acid methyl ester
    3. CAS NO:86296-94-8
    4. Molecular Formula:
    5. Molecular Weight: 360.412
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86296-94-8.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-Acetyl-3-cyano-5-methyl-2,4-diphenyl-2,3-dihydro-1H-pyrrole-3-carboxylic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Acetyl-3-cyano-5-methyl-2,4-diphenyl-2,3-dihydro-1H-pyrrole-3-carboxylic acid methyl ester(86296-94-8)
    11. EPA Substance Registry System: 1-Acetyl-3-cyano-5-methyl-2,4-diphenyl-2,3-dihydro-1H-pyrrole-3-carboxylic acid methyl ester(86296-94-8)

  • 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: 86296-94-8(Hazardous Substances Data)

86296-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86296-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,9 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86296-94:
(7*8)+(6*6)+(5*2)+(4*9)+(3*6)+(2*9)+(1*4)=178
178 % 10 = 8
So 86296-94-8 is a valid CAS Registry Number.

86296-94-8Relevant articles and documents

Addition d'azlactones ylures d'azomethine potentiels a quelques alcenes electrophiles, en milieu anhydride acetique : obtention de pyrrolines-2 et de pyrroles N-acetyles

Yebdri, Okacha,Texier, Fernand

, p. 195 - 201 (2007/10/02)

Azlactones, potential azomethin-ylids, are prepared in situ acetic anhydride from the corresponding α-amino acid, and their addition to electrophilic alkenes RCH=C(X)(Y) leads to N-acetyl Δ2-pyrroline.If X=Y=CN, the pyrroline eliminates HCN and produces a pyrrole.If R=H (acrylic and methacrylic esters and nitriles) the hydrolytic openchain products are obtained.

ORIENTATION DE LA CYCLOADDITION D'OXAZOLONES MESOIONIQUES AUX ALCENES

Yebdri, Okacha,Henri-Rousseau, Olivier,Texier, Fernand

, p. 369 - 372 (2007/10/02)

The regioselectivity of the cycloaddition of mesoionic oxazolones to alkenes has been found to be markedly dependent on the substituent groups present and an explanation is proposed.

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