723262-95-1 Usage
Uses
Used in Pharmaceutical Industry:
(5S)-5,6-DIHYDRO-6,6-DIMETHYL-5-PHENYL-2H-1,4-OXAZIN-2-ONE is used as a pharmaceutical candidate for the development of new drugs due to its potential biological activities and unique molecular structure, which can be exploited to target specific diseases and conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (5S)-5,6-DIHYDRO-6,6-DIMETHYL-5-PHENYL-2H-1,4-OXAZIN-2-ONE serves as a subject of study for understanding its interactions with biological targets and its potential to be modified for enhanced therapeutic effects.
Used in Drug Discovery:
(5S)-5,6-DIHYDRO-6,6-DIMETHYL-5-PHENYL-2H-1,4-OXAZIN-2-ONE is utilized in drug discovery processes to identify its potential as a lead compound for the creation of novel therapeutic agents, given its distinctive stereochemistry and heterocyclic nature.
Check Digit Verification of cas no
The CAS Registry Mumber 723262-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,3,2,6 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 723262-95:
(8*7)+(7*2)+(6*3)+(5*2)+(4*6)+(3*2)+(2*9)+(1*5)=151
151 % 10 = 1
So 723262-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO2/c1-12(2)11(13-8-10(14)15-12)9-6-4-3-5-7-9/h3-8,11H,1-2H3/t11-/m0/s1
723262-95-1Relevant academic research and scientific papers
Stereoselective nucleophilic addition with a new chiral template and its application to the synthesis of optically active α-arylglycine derivatives
Tohma, Shigemitsu,Rikimaru, Kentaro,Endo, Atsushi,Shimamoto, Keiko,Kan, Toshiyuki,Fukuyama, Tohru
, p. 909 - 917 (2007/10/03)
Mannich-type reaction of phenols with iminolactone 4, readily prepared from commercially available phenylglycine, proceeded with high stereoselectivity to give α-arylglycine derivatives. The reaction was also applicable to other electron-rich aromatic compounds, arylboronic acids and other nucleophiles. Additionally, several Lewis acid-promoted addition reactions with iminolactone 4 were accomplished efficiently. These adducts could be converted readily to the corresponding optically active α-amino acid derivatives.
