Welcome to LookChem.com Sign In|Join Free
  • or
1H-Pyrrole-3-carbonitrile, 5-methyl-2,4-diphenyl- is a chemical compound with the molecular formula C18H14N2. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with one nitrogen atom and four carbon atoms. In this specific compound, the pyrrole ring is substituted with a methyl group at the 5-position and two phenyl groups at the 2 and 4 positions. The presence of a carbonitrile group at the 3-position further modifies the structure. 1H-Pyrrole-3-carbonitrile, 5-methyl-2,4-diphenyl- is known for its potential applications in the synthesis of various pharmaceuticals and organic materials due to its unique structure and properties.

86297-00-9

Post Buying Request

86297-00-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

86297-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86297-00-9 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 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86297-00:
(7*8)+(6*6)+(5*2)+(4*9)+(3*7)+(2*0)+(1*0)=159
159 % 10 = 9
So 86297-00-9 is a valid CAS Registry Number.

86297-00-9Downstream Products

86297-00-9Relevant academic research and scientific papers

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.

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 86297-00-9