AE09738
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $16.00 | $11.00 | - + | |
5g | 98% | in stock | $21.00 | $15.00 | - + | |
10g | 98% | in stock | $40.00 | $28.00 | - + | |
25g | 98% | in stock | $68.00 | $48.00 | - + | |
100g | 98% | in stock | $271.00 | $190.00 | - + | |
500g | 98% | in stock | $1,317.00 | $922.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE09738 |
Chemical Name: | 4-Morpholinobenzaldehyde |
CAS Number: | 1204-86-0 |
Molecular Formula: | C11H13NO2 |
Molecular Weight: | 191.2264 |
MDL Number: | MFCD00735826 |
SMILES: | C1COCCN1C2=CC=C(C=C2)C=O |
4-(4-Morpholinyl)benzaldehyde is a key intermediate in chemical synthesis, widely utilized in various organic reactions to introduce functional groups and build complex molecular structures. This versatile compound is a crucial building block in the pharmaceutical industry, particularly in the synthesis of heterocyclic compounds and drugs.In organic synthesis, 4-(4-Morpholinyl)benzaldehyde serves as a valuable starting material for the preparation of diverse compounds due to its reactive aldehyde group and the morpholine moiety. It can undergo various transformations such as nucleophilic addition reactions, condensations, and cyclizations to yield a wide range of substituted derivatives with different functionalities.One common application of 4-(4-Morpholinyl)benzaldehyde is in the formation of Mannich bases, which are essential intermediates in the synthesis of pharmaceuticals and bioactive compounds. By reacting with primary or secondary amines and formaldehyde, this compound can participate in Mannich-type condensation reactions, leading to the formation of Mannich bases with high structural diversity and biological activity.Moreover, 4-(4-Morpholinyl)benzaldehyde can also be employed in the synthesis of various heterocyclic compounds, such as pyrazoles, oxadiazoles, and thiazolidines, through cyclization reactions. These heterocycles are important structural motifs found in many biologically active molecules and can be prepared efficiently using the versatile reactivity of 4-(4-Morpholinyl)benzaldehyde.Overall, the utility of 4-(4-Morpholinyl)benzaldehyde in chemical synthesis lies in its ability to act as a multifunctional building block, facilitating the construction of diverse organic molecules with potential applications in drug discovery, material science, and other fields of chemistry.