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Catalog Number	AR006XI0
Chemical Name	BOC-(S)-3-AMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID
CAS Number	499995-79-8
Molecular Formula	C14H19NO5
Molecular Weight	281.3044
MDL Number	MFCD03427902
SMILES	OC(=O)C[C@@H](c1cccc(c1)O)NC(=O)OC(C)(C)C

(S)-3-((tert-Butoxycarbonyl)amino)-3-(3-hydroxyphenyl)propanoic acid, also known as $name$, is widely utilized in chemical synthesis as a versatile building block due to its unique structural properties. This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials. Specifically, its chiral nature makes it a valuable tool in the creation of enantiopure compounds, essential for pharmaceutical applications where the stereochemistry of molecules profoundly impacts their biological activity.In the field of drug development, (S)-3-((tert-Butoxycarbonyl)amino)-3-(3-hydroxyphenyl)propanoic acid plays a key role in the design and production of new therapeutic agents. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective manipulation of functional groups during the synthesis process, enabling precise control over chemical reactions and yielding high-purity products. Additionally, the 3-hydroxyphenyl moiety provides versatility in introducing aromatic functionalities, which are often essential for enhancing the pharmacological properties of the final compounds.Furthermore, the use of (S)-3-((tert-Butoxycarbonyl)amino)-3-(3-hydroxyphenyl)propanoic acid in chemical synthesis extends beyond the pharmaceutical industry. Its incorporation in the development of specialty chemicals, such as agrochemicals and materials science, showcases its broad applicability and significance in advancing various fields of chemistry. By leveraging the unique molecular structure and reactivity of this compound, researchers can access a diverse array of chemical transformations to produce complex molecules with targeted properties and functionalities.In summary, the strategic utilization of (S)-3-((tert-Butoxycarbonyl)amino)-3-(3-hydroxyphenyl)propanoic acid in chemical synthesis exemplifies its indispensable role as a valuable building block for the creation of diverse compounds with tailored characteristics. Its ability to facilitate the synthesis of enantiopure and functionalized molecules makes it an essential tool for advancing research and innovation across multiple scientific disciplines.

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GHS Pictogram
Signal Word	Warning
UN#	-
Hazard Statements	H302-H315-H319-H335
Precautionary Statements	P261-P280-P301+P312-P302+P352-P305+P351+P338
Class	-
Packing Group	-