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51301-86-1

2-TERT-BUTOXYCARBONYLAMINO-3-(4-CHLORO-PHENYL)-PROPIONIC ACID

Catalog#: AR00DIK5  |   CAS#: 51301-86-1  |   MDL#: MFCD02081080  |   MF: C14H18ClNO4  |   MW: 299.7500

Packsize Purity Price Availability Quantity
250mg 98% $4.00 Global Stock Buy Now Add To Cart
1g 98% $5.00 Global Stock Buy Now Add To Cart
5g 98% $21.00 Global Stock Buy Now Add To Cart
10g 98% $40.00 Global Stock Buy Now Add To Cart
25g 98% $88.00 Global Stock Buy Now Add To Cart
100g 98% $267.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DIK5
Chemical Name 2-TERT-BUTOXYCARBONYLAMINO-3-(4-CHLORO-PHENYL)-PROPIONIC ACID
CAS Number 51301-86-1
Molecular Formula C14H18ClNO4
Molecular Weight 299.7500
MDL Number MFCD02081080
SMILES OC(=O)C(Cc1ccc(cc1)Cl)NC(=O)OC(C)(C)C

The compound 2-((tert-Butoxycarbonyl)amino)-3-(4-chlorophenyl)propanoic acid, commonly referred to as $name$, is a versatile chemical that finds extensive application in chemical synthesis processes. This compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its unique chemical structure allows for efficient manipulation in reactions, making it an essential building block in the synthesis of complex organic molecules.One of the primary uses of $name$ in chemical synthesis is as a protecting group for the amino functionality. The tert-butoxycarbonyl (Boc) group serves to temporarily mask the amine group, providing protection during specific chemical reactions and enabling selective functional group manipulations. This protection strategy is crucial in the synthesis of peptides, pharmaceutical compounds, and natural products, where precise control over the reaction pathways is essential.Additionally, the presence of the 4-chlorophenyl moiety in $name$ offers opportunities for further diversification in synthetic pathways. The chlorophenyl group can participate in various cross-coupling reactions, functionalizations, and transformations, expanding the chemical versatility of the compound in diverse synthetic applications.Overall, the strategic incorporation of 2-((tert-Butoxycarbonyl)amino)-3-(4-chlorophenyl)propanoic acid in chemical synthesis enables chemists to access structurally complex molecules with high efficiency and selectivity. Its role as a protecting group and its reactivity profile make it an indispensable tool for the construction of advanced organic compounds in the fields of pharmaceuticals, materials science, and agrochemical research.
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