120042-09-3 Usage
Description
N-Boc-L-homoserine Methyl Ester 4-Methylbenzenesulfonate is a white solid compound that serves as a crucial intermediate in the synthesis of various organic compounds, particularly in the development of pharmaceuticals and bioactive molecules.
Uses
Used in Pharmaceutical Synthesis:
N-Boc-L-homoserine Methyl Ester 4-Methylbenzenesulfonate is used as a synthetic intermediate for the creation of azidohomoalanine, a functionalizable methionine surrogate. N-Boc-L-homoserine Methyl Ester 4-Methylbenzenesulfonate plays a vital role in the development of novel pharmaceuticals and bioactive molecules, contributing to the advancement of drug discovery and therapeutic applications.
Used in Organic Chemistry:
In the field of organic chemistry, N-Boc-L-homoserine Methyl Ester 4-Methylbenzenesulfonate is utilized as a key building block for the synthesis of complex organic molecules. Its unique structure and reactivity make it a valuable asset in the design and synthesis of new compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
N-Boc-L-homoserine Methyl Ester 4-Methylbenzenesulfonate is also employed in research and development laboratories, where it is used to study the properties and reactivity of various organic compounds. N-Boc-L-homoserine Methyl Ester 4-Methylbenzenesulfonate serves as a model system for understanding the behavior of similar molecules and can be used to develop new synthetic methods and strategies in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 120042-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,0,4 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120042-09:
(8*1)+(7*2)+(6*0)+(5*0)+(4*4)+(3*2)+(2*0)+(1*9)=53
53 % 10 = 3
So 120042-09-3 is a valid CAS Registry Number.
120042-09-3Relevant articles and documents
Synthesis and Biological Evaluation of CF3Se-Substituted α-Amino Acid Derivatives
Han, Zhou-Zhou,Dong, Tao,Ming, Xiao-Xia,Kuang, Fu,Zhang, Cheng-Pan
, p. 3177 - 3180 (2021/07/28)
Several CF3Se-substituted α-amino acid derivatives, such as (R)-2-amino-3-((trifluoromethyl)selanyl)propanoates (5 a/6 a), (S)-2-amino-4-((trifluoromethyl)selanyl)butanoates (5 b/6 b), (2R,3R)-2-amino-3-((trifluoromethyl)selanyl)butanoates (5 c/6 c), (R)-2-((S)-2-amino-3-phenylpropanamido)-3-((trifluoromethyl)selanyl)propanoates (11 a/12 a), and (R)-2-(2-aminoacetamido)-3-((trifluoromethyl)selanyl)propanoates (11 b/12 b), were readily synthesized from natural amino acids and [Me4N][SeCF3]. The primary in vitro cytotoxicity assays revealed that compounds 6 a, 11 a and 12 a were more effective cell growth inhibitors than the other tested CF3Se-substituted derivatives towards MCF-7, HCT116, and SK-OV-3 cells, with their IC50 values being less than 10 μM for MCF-7 and HCT116 cells. This study indicated the potentials of CF3Se moiety as a pharmaceutically relevant group in the design and synthesis of novel biologically active molecules.
