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(2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)aMino)-2-Methylpentanoic acid CAS: 1012341-50-2

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Catalog Number: XD93671
Cas: 1012341-50-2
Molecular Formula: C23H29NO4
Molecular Weight: 383.48
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Product Detail

Product Tags

Catalog Number XD93671
Product Name (2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)aMino)-2-Methylpentanoic acid
CAS 1012341-50-2
Molecular Formula C23H29NO4
Molecular Weight 383.48
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

(2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpentanoic acid is a chemical compound that has various applications in pharmaceutical research and synthetic chemistry. This compound possesses a unique structure and functionality that makes it valuable in different chemical processes.One of the key applications of (2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpentanoic acid is its use as a building block in the synthesis of bioactive molecules. It contains a biphenyl group, which is a common pharmacophore in many drugs. This compound can be utilized to introduce the biphenyl motif into various compounds, potentially leading to the development of new therapeutic agents with enhanced properties.Another important use of (2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpentanoic acid is as a protecting group in organic synthesis. The tert-butoxycarbonyl (Boc) group attached to the amino moiety acts as a temporary shield, allowing selective modifications in other parts of the molecule. This protection strategy is particularly useful in complex multi-step synthesis, providing control over the functional group transformations and ensuring the desired chemical reactions occur at the intended sites.Furthermore, (2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpentanoic acid can play a role as a chiral auxiliary in asymmetric synthesis. Due to its stereocenters, this compound can influence the stereochemistry of reactions and improve the enantioselectivity in the formation of chiral compounds. Chemists can utilize this compound to control the formation of specific enantiomers during chemical transformations.Additionally, (2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpentanoic acid may find application as a reference standard in analytical chemistry. It can be used as a reference compound for analysis and comparison with unknown samples. This is particularly important in pharmaceutical quality control, where the accurate identification and quantification of active ingredients are crucial.In summary, (2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpentanoic acid is a versatile compound with various applications in pharmaceutical research and synthetic chemistry. It can be used as a building block for the synthesis of bioactive molecules, a protecting group during chemical transformations, and a chiral auxiliary to control the stereochemistry of reactions. It may also be employed as a reference standard in analytical chemistry. The unique features and functionality of this compound make it a valuable tool for researchers in the development of new drugs and the synthesis of complex organic molecules.


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    (2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)aMino)-2-Methylpentanoic acid CAS: 1012341-50-2