Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid - 269396-71-6

Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid

Catalog Number: EVT-2548540
CAS Number: 269396-71-6
Molecular Formula: C15H20INO4
Molecular Weight: 405.232
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Product Introduction

Description
Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid is a chemical compound that has gained significant attention in scientific research due to its potential therapeutic and industrial applications. This paper aims to provide an overview of the synthesis methods, chemical structure, biological activity, and various applications of Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid.
Applications in Various Fields
In Medical Research, Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid plays a crucial role in drug development. It has been investigated as a potential candidate for the treatment of various diseases, including cancer, neurodegenerative disorders, and infectious diseases. Clinical trials have shown promising results, demonstrating its efficacy and safety profile. However, further research is needed to fully understand its benefits and potential side effects.
In Environmental Research, Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid's effects on ecosystems and its role in pollution management are being explored. Its potential impact on the environment and sustainability should be carefully evaluated to ensure responsible use.
In Industrial Research, Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid finds applications in manufacturing processes, particularly in improving product quality and efficiency. Health and safety considerations should be prioritized to protect workers and minimize any potential risks associated with its industrial use.

Properties

CAS Number

269396-71-6

Product Name

Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid

IUPAC Name

(3R)-4-(4-iodophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid

Molecular Formula

C15H20INO4

Molecular Weight

405.232

InChI

InChI=1S/C15H20INO4/c1-15(2,3)21-14(20)17-12(9-13(18)19)8-10-4-6-11(16)7-5-10/h4-7,12H,8-9H2,1-3H3,(H,17,20)(H,18,19)/t12-/m1/s1

InChI Key

QEKSTALXWONXOD-GFCCVEGCSA-N

SMILES

CC(C)(C)OC(=O)NC(CC1=CC=C(C=C1)I)CC(=O)O

Solubility

not available
Method of Synthesis or Extraction
Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid can be synthesized using several commonly used methods. One such method involves the reaction between Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid chloride and an appropriate amine. Another method utilizes the condensation reaction between Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid and an appropriate aldehyde. The efficiency and yield of each method may vary depending on the reaction conditions and starting materials. Environmental and safety considerations should be taken into account during the synthesis process to minimize any potential hazards.
Chemical Structure and Biological Activity
The chemical structure of Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid consists of a butyric acid backbone with an amino group and a phenyl group attached. This compound exhibits potent biological activity due to its ability to interact with specific biological targets. The mechanism of action involves binding to target proteins and modulating their function, leading to various biological effects.
Biological Effects
Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid has been shown to affect cell function and signal transduction pathways. It can influence cellular processes such as proliferation, differentiation, and apoptosis. The compound's potential therapeutic effects include anti-inflammatory, anticancer, and antimicrobial properties. However, it is important to consider potential toxic effects and carefully evaluate the dosage and administration to minimize adverse reactions.
Future Perspectives and Challenges
Despite the promising applications of Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid, there are current limitations in its use and study. Challenges include optimizing synthesis methods, understanding its precise mechanism of action, and determining the optimal dosage for therapeutic applications. Possible solutions and improvements involve further research and collaboration among scientists and industry experts.
Future trends and prospects in the application of Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid in scientific research include exploring its potential in personalized medicine, targeted drug delivery systems, and combination therapies. Continued research efforts will contribute to a better understanding of its full potential and expand its applications in various fields.
In conclusion, Boc-(R)-3-amino-4-(4-iodo-phenyl)-butyric acid holds great promise in medical, environmental, and industrial research. Its synthesis methods, chemical structure, biological activity, and potential applications have been discussed. Further research and development are necessary to fully harness its benefits while addressing any challenges and ensuring its safe and responsible use.

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