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AB45657

37535-58-3 | Boc-D-4-pyridylalanine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $19.00 $13.00 -   +
1g 97% in stock $44.00 $31.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB45657
Chemical Name: Boc-D-4-pyridylalanine
CAS Number: 37535-58-3
Molecular Formula: C13H18N2O4
Molecular Weight: 266.293
MDL Number: MFCD00672529
SMILES: OC(=O)[C@@H](Cc1ccncc1)NC(=O)OC(C)(C)C

 

Computed Properties
Complexity: 319  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 19  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 6  
XLogP3: 1.4  

 

 

Upstream Synthesis Route
  • Boc-3-(4-pyridyl)-D-alanine is a versatile and widely used compound in chemical synthesis due to its unique properties and reactivity. This compound, with a tert-butoxycarbonyl (Boc) protecting group, plays a crucial role in peptide and small molecule synthesis.In chemical synthesis, Boc-3-(4-pyridyl)-D-alanine serves as a key building block for the construction of complex molecules, specifically peptides. The Boc protecting group temporarily shields the amino group, allowing for selective reactions and preventing unwanted side reactions. This compound can be incorporated into peptide chains to introduce specific functional groups or modified amino acids, expanding the diversity of synthesized peptides.Moreover, the 4-pyridyl moiety in Boc-3-(4-pyridyl)-D-alanine adds additional reactivity and versatility to the compound. The pyridine ring can participate in various chemical transformations, such as cross-coupling reactions or metal-catalyzed transformations, enabling further modifications and functionalizations of the synthesized molecules.Overall, Boc-3-(4-pyridyl)-D-alanine is an indispensable tool in chemical synthesis, particularly in peptide chemistry, owing to its strategic placement of the Boc protecting group and the unique reactivity of the 4-pyridyl functionality. By utilizing this compound, chemists can efficiently and selectively synthesize diverse molecules with tailored functionalities for various applications in drug discovery, materials science, and chemical biology.
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