Boc-β-(2-thienyl)-DL-Ala-OH, with the CAS number 78512-39-7, is a chemical compound that belongs to the class of amino acids, specifically a derivative of alanine. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group used in peptide synthesis, which helps to prevent unwanted reactions during the synthesis process. The presence of the β-(2-thienyl) moiety indicates that this compound contains a thienyl group, which is a five-membered aromatic ring containing sulfur, contributing to its unique chemical properties and potential biological activity. This compound is typically used in organic synthesis and medicinal chemistry, particularly in the development of peptide-based drugs. Its structure allows for various modifications, making it versatile in research applications. The compound is generally stable under standard laboratory conditions but should be handled with care, following appropriate safety protocols. As with many amino acid derivatives, it may exhibit specific solubility characteristics and reactivity, which are important for its application in synthetic chemistry.

Boc-.beta.-(2-thienyl)-DL-Ala-OH

78512-39-7: Boc-β-(2-thienyl)-DL-Ala-OH, with the CAS number 78512-39-7, is a chemical compound that belongs to the class of amino acids, specifically a derivative of alanine. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group used in peptide synthesis, which helps to prevent unwanted reactions during the synthesis process. The presence of the β-(2-thienyl) moiety indicates that this compound contains a thienyl group, which is a five-membered aromatic ring containing sulfur, contributing to its unique chemical properties and potential biological activity. This compound is typically used in organic synthesis and medicinal chemistry, particularly in the development of peptide-based drugs. Its structure allows for various modifications, making it versatile in research applications. The compound is generally stable under standard laboratory conditions but should be handled with care, following appropriate safety protocols. As with many amino acid derivatives, it may exhibit specific solubility characteristics and reactivity, which are important for its application in synthetic chemistry.

CAS 78512-39-7

Boc-.beta.-(2-thienyl)-DL-Ala-OH

BOC-β-(2-THIENYL)-DL-ALA-OH

Ref: IN-DA00G645

2-((tert-Butoxycarbonyl)amino)-3-(thiophen-2-yl)propanoic acid

Ref: 10-F242408