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4-Aminobenzaldehyde CAS:556-18-3

Short Description:

Catalog Number: XD96240
Cas: 556-18-3
Molecular Formula: C7H7NO
Molecular Weight: 121.14
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Product Detail

Product Tags

Catalog Number XD96240
Product Name 4-Aminobenzaldehyde
CAS 556-18-3
Molecular Formula C7H7NO
Molecular Weight 121.14
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

4-Aminobenzaldehyde, also known as p-aminobenzaldehyde or 4-ABA, is a chemical compound that exhibits various effects and applications due to its unique structure and properties.One significant effect of 4-Aminobenzaldehyde is its ability to act as a versatile building block in organic synthesis. It possesses both an amino group (-NH2) and an aldehyde group (-CHO), making it amenable to various reactions such as condensation, nucleophilic addition, and Schiff base formation. These reactions allow for the creation of complex organic compounds and derivatives, which find applications in the synthesis of pharmaceuticals, dyes, and other functional materials.In the field of pharmaceuticals, 4-Aminobenzaldehyde is utilized as an intermediate in the synthesis of biologically active compounds. The amino group present in its structure allows for the introduction of diverse functionalities and pharmacophores. This enables the modification of the compound to enhance its biological properties, such as improved bioavailability, increased target specificity, or reduced toxicity. These modified derivatives can be employed in the development of drugs targeting various diseases, including cancer, cardiovascular disorders, and microbial infections.Another effect of 4-Aminobenzaldehyde is its role in the production of dyes and colorants. Its aromatic structure and reactive functional groups make it a suitable precursor for the synthesis of azo and anthraquinone dyes. These dyes find applications in textiles, plastics, and printing inks, providing vibrant and durable colors to various products. Additionally, 4-Aminobenzaldehyde derivatives can also be used as fluorescent tags or probes for imaging and sensing applications, as they exhibit distinct optical properties.Furthermore, 4-Aminobenzaldehyde can act as a reducing agent due to the presence of the aldehyde group. It can undergo condensation reactions with various carbonyl compounds, such as sugars or ketones, resulting in the formation of reduced products. This property makes 4-Aminobenzaldehyde useful in the synthesis of sugar derivatives, amino sugars, and other carbohydrate-based compounds, which have applications in the food industry, pharmaceuticals, and biochemical research.In summary, 4-Aminobenzaldehyde possesses several effects and applications. It serves as a versatile building block in organic synthesis, allowing for the creation of complex compounds. Its role in pharmaceutical synthesis enables the development of biologically active molecules. Additionally, it finds applications in dye production and acts as a reducing agent in the synthesis of carbohydrate derivatives. With its diverse properties, 4-Aminobenzaldehyde proves to be a valuable compound with broad applications in different areas of chemistry and industry.


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    4-Aminobenzaldehyde CAS:556-18-3