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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyrimidines  > 2-(4,6-Dichloropyrimidin-5-yl)acetaldehyde

AA82405

16019-33-3 | 2-(4,6-Dichloropyrimidin-5-yl)acetaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $10.00 $7.00 -   +
1g 95% in stock $12.00 $8.00 -   +
5g 95% in stock $18.00 $12.00 -   +
10g 95% in stock $28.00 $19.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA82405
Chemical Name: 2-(4,6-Dichloropyrimidin-5-yl)acetaldehyde
CAS Number: 16019-33-3
Molecular Formula: C6H4Cl2N2O
Molecular Weight: 191.0148
MDL Number: MFCD09991563
SMILES: O=CCc1c(Cl)ncnc1Cl

 

Computed Properties
Complexity: 135  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 2  
XLogP3: 1.5  

 

 

Upstream Synthesis Route
  • The chemical compound 2-(4,6-Dichloropyrimidin-5-yl)acetaldehyde, commonly referred to as $name$, serves as a versatile building block in chemical synthesis due to its unique reactivity and structural properties. Its application in synthetic chemistry extends to various fields, including pharmaceuticals, agrochemicals, and materials science. In chemical synthesis, $name$ is often utilized as a key intermediate in the production of heterocyclic compounds with diverse functionalities. Its aldehyde group allows for selective reactions with nucleophiles, such as amines and hydrazines, enabling the creation of novel structures through condensation and cyclization processes. The presence of the dichloropyrimidine moiety further enhances the reactivity of $name$ by participating in coupling reactions to introduce additional substituents or functional groups.Moreover, the unique electronic properties of 2-(4,6-Dichloropyrimidin-5-yl)acetaldehyde make it a valuable precursor in the synthesis of biologically active molecules and potential drug candidates. Its ability to undergo regioselective transformations under mild reaction conditions contributes to the efficiency and selectivity of complex molecule assembly. Additionally, the accessibility of diverse synthetic routes to functionalize $name$ provides synthetic chemists with flexibility in designing and optimizing chemical pathways for the targeted synthesis of desired compounds.Overall, the strategic incorporation of 2-(4,6-Dichloropyrimidin-5-yl)acetaldehyde in chemical synthesis offers a powerful tool for building molecular complexity, facilitating the discovery and development of new chemical entities with applications across various industrial sectors.
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