Welcome to LookChem.com Sign In|Join Free
  • or
2-(2,5-dibromophenyl)isoindoline-1,3-dione is a chemical compound characterized by its unique structure and properties. It is a derivative of isoindoline-1,3-dione, with a 2,5-dibromophenyl group attached at the 2-position. This molecule features a fused ring system, consisting of an isoindoline core and a phenyl ring, with two bromine atoms substituting the 2nd and 5th positions of the phenyl ring. The compound is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its ability to form stable complexes and interact with other molecules. Its chemical formula is C14H7Br2NO2, and it has a molecular weight of 376.02 g/mol. The compound's structure and properties make it an interesting subject for further research and development in the field of organic chemistry.

3481-16-1

Post Buying Request

3481-16-1 Suppliers

Recommended suppliers

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

3481-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3481-16-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,8 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3481-16:
(6*3)+(5*4)+(4*8)+(3*1)+(2*1)+(1*6)=81
81 % 10 = 1
So 3481-16-1 is a valid CAS Registry Number.

3481-16-1Downstream Products

3481-16-1Relevant academic research and scientific papers

Aza-DielsAlder reaction between N-aryl-1-oxo-1H-isoindolium ions and tert-enamides: Steric effects on reaction outcome

Jha, Amitabh,Chou, Ting-Yi,ALJaroudi, Zainab,Ellis, Bobby D.,Cameron, T. Stanley

supporting information, p. 848 - 857 (2014/05/06)

The synthesis of 5-substituted 6,6a-dihydroisoindolo[2,1-a]quinolin-11(5H)- ones via [4 + 2] imino-DielsAlder cyclization from N-aryl-3- hydroxyisoindolinones and N-vinyl lactams under Lewis acid-catalysed anhydrous conditions is reported. Reactions of N-(2-substituted-aryl)-3- hydroxyisoindolinones with N-vinylpyrrolidone under identical conditions resulted in the formation of 2-(2-substitued-aryl)-3-(2-(2-oxopyrrolidin-1-yl) vinyl)isoindolin-1-one analogues indicating steric hinderance as the cause of deviation. The probable mechanism of the reaction based on the results from X-ray crystallography and molecular modelling is discussed.

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 3481-16-1