Understanding the precise chemical profile of specialized compounds is crucial for their effective application in research and development. Boc-(R)-3-Amino-4-(1-naphthyl)-butyric Acid, identified by CAS number 190190-49-9, is a prime example of such a compound. This molecule is a protected amino acid derivative, featuring a tert-butyloxycarbonyl (Boc) group on the amine and a naphthyl substituent on the side chain. Its structure, specifically its (R)-chirality, makes it a valuable tool for chemists engaged in stereoselective synthesis, particularly within the pharmaceutical industry.

The Boc protecting group serves a vital role in peptide synthesis and other organic transformations. It moderates the reactivity of the amine group, preventing unwanted side reactions during coupling or modification steps. This protection is readily removable under mild acidic conditions, allowing for controlled peptide chain elongation or further functionalization. The naphthyl group, a fused bicyclic aromatic system, introduces significant hydrophobicity and steric bulk to the molecule. This characteristic can influence the conformational preferences of peptides into which it is incorporated, potentially enhancing binding affinities or stability.

As a manufacturer and supplier of this specialized chemical, we focus on delivering material with consistent purity and defined stereochemistry. The appearance of Boc-(R)-3-Amino-4-(1-naphthyl)-butyric Acid is typically described as a white to off-white solid or powder, indicative of its high purity. For researchers looking to purchase this compound, understanding these fundamental properties is key to selecting the right material for their specific application, whether it's in drug discovery, material science, or biochemical assays.

The value of Boc-(R)-3-Amino-4-(1-naphthyl)-butyric Acid lies in its versatility as a chiral building block. It can be readily coupled with other amino acids or functionalized molecules using standard peptide coupling reagents. Its incorporation into complex molecular architectures allows for the precise introduction of chirality and specific side-chain functionalities. This precision is essential for developing molecules with targeted biological activities, such as pharmaceuticals or advanced materials. For those seeking to buy this intermediate, engaging with a reputable supplier in China ensures access to high-quality material backed by rigorous quality control.

In summary, the chemical profile of Boc-(R)-3-Amino-4-(1-naphthyl)-butyric Acid—its protected amine, its characteristic naphthyl side chain, and its defined (R)-chirality—positions it as an indispensable component in modern organic synthesis. Its reliable availability from trusted manufacturers and suppliers is crucial for researchers pushing the boundaries of chemical innovation.