115011-73-9 Usage
General Description
3-Trityl-5-oxazolidinone is a chemical compound with the molecular formula C22H19NO2. It is a five-membered heterocycle containing an oxygen atom and a nitrogen atom, and it is commonly used as a precursor in organic synthesis. The trityl group, which is a triphenylmethyl substituent, is attached to the nitrogen atom, providing stability and facilitating various reactions. 3-Trityl-5-oxazolidinone has been employed in the synthesis of various pharmaceuticals and natural products due to its reactivity and versatility. It has also been studied for its potential biological activities, including antimicrobial and antitumor properties. Overall, 3-Trityl-5-oxazolidinone is a valuable and multifunctional chemical compound with applications in both organic chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 115011-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,0,1 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115011-73:
(8*1)+(7*1)+(6*5)+(5*0)+(4*1)+(3*1)+(2*7)+(1*3)=69
69 % 10 = 9
So 115011-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C22H19NO2/c24-21-16-23(17-25-21)22(18-10-4-1-5-11-18,19-12-6-2-7-13-19)20-14-8-3-9-15-20/h1-15H,16-17H2
115011-73-9Relevant articles and documents
Simple Generation of Nonstabilized Azomethine Ylides through Decarboxylative Condensation of α-Amino Acids with Carbonyl Compounds via 5-Oxazolidinone Intermediates
Tsuge, Otohiko,Kanemasa, Shuji,Ohe, Masayuki,Takenaka, Shigeori
, p. 4079 - 4090 (2007/10/02)
Heating α-amino acids with a variety of carbonyl compounds generates N-unsubstituted or N-substituted azomethine ylides of nonstabilized types through the elimination of water and carbon dioxide.The ylides are captured by olefinic, acetylenic, and carbonyl dipolarophiles producing pyrrolidines, pyrrolines, and oxazolidines.The reaction involves intermediary 5-oxazolidinones which can be sometimes isolated.Some synthetic equivalents of parent azomethine ylide, methaniminium methylide, are accessible by this route.
