73200-21-2 Usage
General Description
1-[(Acetyloxy)phenylacetyl]-pyrrolidine is a chemical compound that belongs to the group of pyrrolidinecarboxylic acids. It is a derivative of pyrrolidine and is formed by the attachment of an acetyloxyphenylacetyl group to the pyrrolidine ring. 1-[(ACETYLOXY)PHENYLACETYL]-PYRROLIDINE is commonly used as an intermediate in the synthesis of pharmaceuticals and in the study of structure-activity relationships of bioactive compounds. It has potential applications in the field of medicinal chemistry due to its ability to interact with biological targets and modulate physiological processes. Additionally, it may have potential uses in drug discovery and development as a starting material for the synthesis of novel bioactive compounds.
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 articles and documents
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.
