Welcome to LookChem.com Sign In|Join Free
  • or
2-Acetyl-3,4-diethyl-pyrrol is a heterocyclic organic compound characterized by a pyrrole ring structure, which is a five-membered aromatic ring containing one nitrogen atom. This specific compound features an acetyl group (a two-carbon ketone) attached to the 2-position of the pyrrole ring, and two ethyl groups (each consisting of two carbon atoms) attached to the 3 and 4 positions, respectively. The compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and reactivity. It is important to note that handling and usage of 2-Acetyl-3,4-diethyl-pyrrol should be done with caution, as it may have potential health and environmental impacts, and it is typically used in a controlled laboratory setting by trained professionals.

2169-20-2

Post Buying Request

2169-20-2 Suppliers

Recommended suppliers

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

2169-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2169-20-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2169-20:
(6*2)+(5*1)+(4*6)+(3*9)+(2*2)+(1*0)=72
72 % 10 = 2
So 2169-20-2 is a valid CAS Registry Number.

2169-20-2Downstream Products

2169-20-2Relevant academic research and scientific papers

One-Pot Synthesis of Butadiyne-Bridged Bipyrrole Derivatives and Bisporphyrin

Kishore, M. V. Nanda,Panda, Pradeepta K.

, p. 5197 - 5203 (2017)

Butadiyne-bridged bipyrroles were prepared from 2-iodopyrroles and trimethylsilylacetylene through a facile one-pot synthesis involving a modified Sonogashira coupling reaction and in situ aerobic oxidative coupling of the acetylenic pyrroles; the products were obtained in yields of 31–72 % depending on the substituents on the pyrrole. The acetylene-bridged diacids obtained from the hydrolysis of the corresponding ester derivatives are highly stable, unlike most reported oligopyrrolic diacids. This protocol could be easily extended towards the synthesis of butadiyne-bridged bisporphyrins.

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 2169-20-2