1260592-58-2 Usage
Derivative of butanoic acid
The compound is derived from butanoic acid, a four-carbon carboxylic acid.
Amino and carboxylic acid functional groups
The compound contains both an amino group (-NH2) and a carboxylic acid group (-COOH), which can participate in various chemical reactions.
Protecting group for amino acids
The compound is often used in organic synthesis to protect amino acids from unwanted reactions during synthetic processes.
Potential applications in pharmaceutical industry
The compound has potential applications in the development of new drugs due to its unique structure and functional groups.
3-chlorophenyl substituent
The presence of a 3-chlorophenyl group in the compound may impart specific properties or functions, making it useful for targeted applications in medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1260592-58-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,5,9 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1260592-58:
(9*1)+(8*2)+(7*6)+(6*0)+(5*5)+(4*9)+(3*2)+(2*5)+(1*8)=152
152 % 10 = 2
So 1260592-58-2 is a valid CAS Registry Number.
1260592-58-2Relevant academic research and scientific papers
Synthesis of γ-oxo γ-aryl and γ-aryl α-amino acids from aromatic aldehydes and serine
Chacko, Shibin,Ramapanicker, Ramesh
, p. 7120 - 7128 (2013/02/21)
γ-Oxo α-amino acids and γ-aryl α-amino acids are compounds with very interesting biological properties and are active components of many drug molecules. Oxo amino acids are also used as synthetic precursors for a number of unnatural amino acids and amino alcohols. We report a very efficient synthesis of such compounds through the coupling of aromatic dithianes, prepared from aromatic aldehydes and an iodide derivative of serine. The dithiane groups in compounds thus obtained can be either hydrolyzed or reduced to generate 4-oxo-4-aryl or 4-aryl 2-amino butanol derivatives, respectively, which, on further transformations, can be converted into the title compounds. Starting with L-serine provides the corresponding D-amino acids with complete enantiopurity. The reported method is economically viable and complements the existing methods, which rely largely on cross-coupling reactions.
