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4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl CAS: 147118-37-4

Short Description:

Catalog Number: XD93414
Cas: 147118-37-4
Molecular Formula: C16H18FN3O3S
Molecular Weight: 351.4
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Product Detail

Product Tags

Catalog Number XD93414
Product Name 4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl
CAS 147118-37-4
Molecular Formula C16H18FN3O3S
Molecular Weight 351.4
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl, also known as FIMPA, is a chemical compound with a complex structure that has potential applications in pharmaceutical research and drug development. It is classified as a pyrimidine derivative with a formyl group attached to the 5th carbon atom, and a 4-fluorophenyl and an isopropyl group attached to the 4th and 6th carbon atoms, respectively.One of the important applications of FIMPA is in the field of cancer research. Pyrimidine derivatives have been extensively studied for their antitumor properties, and FIMPA shows potential as an anticancer agent. Its structural features make it a promising candidate for inhibiting key enzymes or receptors involved in tumor growth and progression. Researchers can modify FIMPA's structure further to enhance its potency, selectivity, and pharmacokinetic properties for more effective cancer treatment.Furthermore, FIMPA can also act as a molecular scaffold for developing drug candidates targeting other diseases. Its unique structure allows for the attachment of different functional groups, which can play a crucial role in interacting with specific molecular targets. This versatility makes FIMPA a valuable tool in medicinal chemistry for developing novel therapeutic agents against various diseases such as neurological disorders or infectious diseases.In addition to its potential therapeutic applications, FIMPA can be utilized in the synthesis of other complex organic compounds. Its reactive functional groups, such as the formyl and sulfonyl groups, can serve as sites for further chemical modifications. Researchers can use FIMPA as a starting material or intermediate compound to access different derivatives, which can be screened for their biological activities or used as building blocks for the synthesis of more complex molecules.Overall, 4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl (FIMPA) exhibits promising potential in various areas of pharmaceutical research and drug development. Its unique structure and functional groups make it an important tool for designing new drug candidates or synthesizing complex organic compounds. Further exploration and optimization of FIMPA's properties can lead to the discovery of novel therapeutic agents and contribute to advancements in the field of medicinal chemistry.


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    4-(4-Fluorophenyl)-6-Isopropyl-2-[(N-Methyl-N-Methylsulfonyl)Amino]Pyrimidinyl-5-Yl-Formyl CAS: 147118-37-4