73200-21-2 Usage
Uses
Used in Pharmaceutical Industry:
1-[(ACETYLOXY)PHENYLACETYL]-PYRROLIDINE is used as an intermediate in the synthesis of pharmaceuticals for its ability to interact with biological targets and modulate physiological processes. This allows for the development of new drugs with potential therapeutic applications.
Used in Medicinal Chemistry Research:
1-[(ACETYLOXY)PHENYLACETYL]-PYRROLIDINE is used in the study of structure-activity relationships of bioactive compounds. This helps researchers understand the relationship between the chemical structure of a compound and its biological activity, which is crucial for the design and optimization of new drugs.
Used in Drug Discovery and Development:
1-[(ACETYLOXY)PHENYLACETYL]-PYRROLIDINE is used as a starting material for the synthesis of novel bioactive compounds. Its potential applications in drug discovery and development make it a valuable tool for creating new therapeutic agents with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 73200-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,0 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73200-21:
(7*7)+(6*3)+(5*2)+(4*0)+(3*0)+(2*2)+(1*1)=82
82 % 10 = 2
So 73200-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO3/c1-11(16)18-13(12-7-3-2-4-8-12)14(17)15-9-5-6-10-15/h2-4,7-8,13H,5-6,9-10H2,1H3
73200-21-2Relevant academic research and scientific papers
Macrocyclic Lactone Formation through Sulfide Contraction. Synthesis of (+/-)-Diplodialide A
Ireland, Robert E.,Brown, Frank R.
, p. 1868 - 1880 (2007/10/02)
A methodology for the synthesis of macrocyclic β-keto-lactones from ω-hydroxy thioamides is described.The hydroxy thioamides were esterified with chloroacetyl chloride, and the resulting chloro esters underwent Eschenmoser sulfide contraction when treated with sodium iodide, diisopropylethylamine, and triethyl phosphite in acetonitrile.The β-keto lactones were obtained in 25-58 percent yield.The utility of the method was demonstrated by synthesis of diplodialide A.
