Boc-β-(2-thienyl)-D-Ala-OH DCHA, with the CAS number 78452-59-2, is a chemical compound that features a protected amino acid structure. The "Boc" (tert-butyloxycarbonyl) group serves as a protective moiety for the amino group, facilitating the synthesis and handling of the compound in various chemical reactions. The β-(2-thienyl) moiety indicates the presence of a thienyl group, which contributes to the compound's unique properties, including potential biological activity. The DCHA (dichloroacetate) component suggests that this compound may be involved in specific applications, possibly in medicinal chemistry or peptide synthesis. The presence of the D-amino acid configuration (D-Ala) can influence the compound's interaction with biological systems, as D-amino acids often exhibit different properties compared to their L-counterparts. Overall, this compound is of interest in research areas such as drug development and peptide chemistry, where modifications to amino acids can lead to enhanced stability and bioactivity.

Boc-.beta.-(2-thienyl)-D-Ala-OH . DCHA

78452-59-2: Boc-β-(2-thienyl)-D-Ala-OH DCHA, with the CAS number 78452-59-2, is a chemical compound that features a protected amino acid structure. The "Boc" (tert-butyloxycarbonyl) group serves as a protective moiety for the amino group, facilitating the synthesis and handling of the compound in various chemical reactions. The β-(2-thienyl) moiety indicates the presence of a thienyl group, which contributes to the compound's unique properties, including potential biological activity. The DCHA (dichloroacetate) component suggests that this compound may be involved in specific applications, possibly in medicinal chemistry or peptide synthesis. The presence of the D-amino acid configuration (D-Ala) can influence the compound's interaction with biological systems, as D-amino acids often exhibit different properties compared to their L-counterparts. Overall, this compound is of interest in research areas such as drug development and peptide chemistry, where modifications to amino acids can lead to enhanced stability and bioactivity.

CAS 78452-59-2

Boc-.beta.-(2-thienyl)-D-Ala-OH . DCHA

Boc-β-(2-thienyl)-D-Ala-OH DCHA

Ref: IN-DA00G2KJ