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AB50200

10338-57-5 | 4-Piperidinobenzaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $19.00 $13.00 -   +
5g 95% in stock $47.00 $33.00 -   +
25g 95% in stock $177.00 $124.00 -   +
100g 95% in stock $538.00 $377.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB50200
Chemical Name: 4-Piperidinobenzaldehyde
CAS Number: 10338-57-5
Molecular Formula: C12H15NO
Molecular Weight: 189.2536
MDL Number: MFCD00778395
SMILES: O=Cc1ccc(cc1)N1CCCCC1
NSC Number: 156549

 

Computed Properties
Complexity: 179  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 2  
XLogP3: 2.9  

 

 

Upstream Synthesis Route
  • 4-(Piperidin-1-yl)benzaldehyde is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals.One of the key applications of 4-(Piperidin-1-yl)benzaldehyde is its role as a starting material in the synthesis of heterocyclic compounds. By reacting with different nucleophiles or electrophiles, it can undergo a variety of transformations to generate complex structures with diverse functionalities. This compound is particularly useful in forming fused heterocycles, which are prevalent in many bioactive molecules.Furthermore, 4-(Piperidin-1-yl)benzaldehyde is often employed in the preparation of ligands for coordination chemistry or as a precursor for the synthesis of chiral compounds. Its ability to undergo selective functionalization reactions makes it a valuable tool for accessing stereochemically complex molecules with high enantiomeric purity.Overall, the versatility and reactivity of 4-(Piperidin-1-yl)benzaldehyde make it a valuable component in the toolbox of synthetic chemists for building structurally diverse and biologically active compounds.
Literature
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