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67843-72-5

Z-β-D-HomoAla-OH

Catalog#: AR003W4B  |   CAS#: 67843-72-5  |   MDL#: MFCD06223032  |   MF: C12H15NO4  |   MW: 237.2518

Packsize Purity Price Availability Quantity
250mg 97% $5.00 Global Stock Buy Now Add To Cart
1g 97% $7.00 Global Stock Buy Now Add To Cart
5g 97% $30.00 Global Stock Buy Now Add To Cart
25g 97% $143.00 Global Stock Buy Now Add To Cart
100g 97% $540.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003W4B
Chemical Name Z-β-D-HomoAla-OH
CAS Number 67843-72-5
Molecular Formula C12H15NO4
Molecular Weight 237.2518
MDL Number MFCD06223032
SMILES C[C@H](CC(=O)O)NC(=O)OCc1ccccc1

(R)-3-(((Benzyloxy)carbonyl)amino)butanoic acid, also known as BOC-Butanoic acid, is a versatile chemical compound widely utilized in organic synthesis. Due to its unique structure and properties, BOC-Butanoic acid plays a crucial role in various chemical reactions and as a valuable building block for the preparation of complex molecules.One of the key applications of BOC-Butanoic acid in chemical synthesis is as a protecting group in peptide synthesis. In peptide chemistry, the BOC (tert-butyloxycarbonyl) group serves as a temporary shield for the amino group of amino acids, preventing unwanted side reactions during the peptide bond formation. By selectively deprotecting the BOC group under specific conditions, chemists can control the order and direction of peptide coupling reactions, leading to the efficient and precise assembly of peptides and proteins.Moreover, BOC-Butanoic acid can also be employed as a precursor for the synthesis of various bioactive compounds, pharmaceuticals, and natural products. Its ability to undergo functional group transformations and participate in diverse chemical reactions makes it a valuable starting material for the creation of molecular libraries and drug discovery research.Overall, the use of (R)-3-(((Benzyloxy)carbonyl)amino)butanoic acid in chemical synthesis exemplifies its importance as a strategic tool for building complex molecules with precision and efficiency. Its versatility and compatibility with a wide range of synthetic methodologies make it an indispensable resource for researchers and chemists working in the field of organic chemistry.
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