Benzenepropanoic acid, b-[[(1,1-dimethylethoxy)carbonyl]amino]-,methyl ester, (bS)-|190189-97-0,AngeneChemical

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Benzenepropanoic acid, b-[[(1,1-dimethylethoxy)carbonyl]amino]-,methyl ester, (bS)-

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Chemical Name:	Benzenepropanoic acid, b-[[(1,1-dimethylethoxy)carbonyl]amino]-,methyl ester, (bS)-
CAS Number:	190189-97-0
Product Number:	AG002EE5(AGN-PC-0QJIY1)
Synonyms:
MDL No:
Molecular Formula:	C15H21NO4
Molecular Weight:	279.3315

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Identification/Properties

Properties

MP:

95-96℃

Storage:

2-8℃;

Form:

Solid

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NMR Spectrum

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Chemical Structure

The application of Methyl (3S)-3-Boc-amino-3-phenylpropionate in chemical synthesis is crucial in the field of organic chemistry. This compound serves as a versatile building block for the synthesis of various complex molecules due to its unique structural characteristics. By possessing both an amino group and a phenyl group, Methyl (3S)-3-Boc-amino-3-phenylpropionate can participate in diverse chemical reactions, including amide bond formation, acylation, and peptide synthesis. Its Boc-protected amine group allows for selective deprotection under mild conditions, making it a valuable tool in the controlled modification of molecules. Additionally, the phenyl group provides aromaticity and steric properties that influence the compound's reactivity and overall behavior in chemical reactions. In summary, the strategic use of Methyl (3S)-3-Boc-amino-3-phenylpropionate in chemical synthesis enables the efficient construction of intricate organic compounds with tailored functionalities and structures.