78452-55-8 Usage
Uses
Used in Chemical Synthesis:
BOC-D-2-THIENYLALANINE is used as a key building block for the synthesis of various complex organic molecules. Its unique thiophene ring and alanine backbone make it a valuable component in the development of novel chemical compounds with potential applications in various industries.
Used in Peptide Chemistry:
In peptide chemistry, BOC-D-2-THIENYLALANINE serves as an essential amino acid analog, which can be incorporated into peptide sequences to create new peptide-based drugs, agonists, or antagonists. Its distinct properties can influence the overall structure, stability, and biological activity of the resulting peptides.
Used in Pharmaceutical Industry:
BOC-D-2-THIENYLALANINE is used as an intermediate in the development of new pharmaceuticals, particularly those targeting specific biological receptors or enzymes. Its unique structural features can be exploited to design drugs with improved selectivity, potency, and reduced side effects.
Used in Research and Development:
BOC-D-2-THIENYLALANINE is utilized as a research tool in various scientific studies, including the investigation of protein structure, function, and interactions. It can also be employed in the development of new analytical methods and techniques for the detection and quantification of biologically relevant molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 78452-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,5 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78452-55:
(7*7)+(6*8)+(5*4)+(4*5)+(3*2)+(2*5)+(1*5)=158
158 % 10 = 8
So 78452-55-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO4S/c1-12(2,3)17-11(16)13-9(10(14)15)7-8-5-4-6-18-8/h4-6,9H,7H2,1-3H3,(H,13,16)(H,14,15)/p-1/t9-/m1/s1
78452-55-8Relevant academic research and scientific papers
RESOLUTION OF β-2-THIENYLALANINE ENANTIOMERS BY A CONVENIENT METHOD
Lipkowski, Andrzej W.,Flouret, George
, p. 2225 - 2228 (2007/10/02)
t-Butyloxycarbonyl derivatives of D- and L-β-2-thienylalanine were prepared by resolution of t-butyloxycarbonyl-D,L-β-2-thienylalanine with (S)- or (R)-α-phenylethylamine.The enantiomeric salts of t-butyloxycarbonyl-amino acids, were converted to t-butylo
