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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridazines  > 4-Bromo-5-chloro-3(2H)-pyridazinone

AI12537

119729-96-3 | 4-Bromo-5-chloro-3(2H)-pyridazinone

Packsize Purity Availability Price Discounted Price    Quantity
100mg 96% in stock $163.00 $114.00 -   +
250mg 96% in stock $251.00 $176.00 -   +
1g 96% in stock $558.00 $391.00 -   +
5g 96% in stock $1,879.00 $1,316.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AI12537
Chemical Name: 4-Bromo-5-chloro-3(2H)-pyridazinone
CAS Number: 119729-96-3
Molecular Formula: C4H2BrClN2O
Molecular Weight: 209.42848000000004
MDL Number: MFCD23106328
SMILES: Clc1cn[nH]c(=O)c1Br

 

Computed Properties
Complexity: 211  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
XLogP3: 1  

 

 

Upstream Synthesis Route
  • 4-Bromo-5-chloropyridazin-3(2H)-one, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in various organic reactions due to its unique chemical properties.In chemical synthesis, 4-Bromo-5-chloropyridazin-3(2H)-one is commonly employed as a building block to introduce specific functional groups into organic molecules. It serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. The presence of both bromine and chlorine atoms on the pyridazinone ring allows for diverse reactivity and enables the selective modification of molecules in a controlled manner.Furthermore, 4-Bromo-5-chloropyridazin-3(2H)-one can participate in cross-coupling reactions, nucleophilic substitutions, and other transformations to create complex molecular structures. Its versatility and compatibility with a wide range of reagents make it a valuable tool in organic synthesis for the preparation of novel compounds with potentially important biological or industrial applications.
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