245728-73-8 Usage
Description
2-[(1R)-3-HYDROXY-1-METHYLPROPYL]-1H-ISOINDOLE-1,3(2H)-DIONE is a chemical compound with the molecular formula C12H13NO3. It belongs to the class of isoindole-1,3(2H)-dione derivatives, which are known for their potential pharmacological properties and use in the synthesis of pharmaceuticals. This specific compound features a hydroxyl group and a methyl group attached to a chiral carbon, endowing it with stereochemical properties. Its potential applications in the pharmaceutical industry include drug development and as a research tool in biological studies. Further research is necessary to explore its specific uses and effects.
Uses
Used in Pharmaceutical Industry:
2-[(1R)-3-HYDROXY-1-METHYLPROPYL]-1H-ISOINDOLE-1,3(2H)-DIONE is used as a chemical intermediate for the synthesis of pharmaceuticals due to its unique structure and potential pharmacological properties.
Used in Drug Development:
2-[(1R)-3-HYDROXY-1-METHYLPROPYL]-1H-ISOINDOLE-1,3(2H)-DIONE serves as a promising candidate in drug development, as its stereochemistry and functional groups may contribute to the design of novel therapeutic agents with specific biological activities.
Used in Biological Research:
2-[(1R)-3-HYDROXY-1-METHYLPROPYL]-1H-ISOINDOLE-1,3(2H)-DIONE is utilized as a research tool in biological studies to investigate its interactions with biological targets and explore its potential as a lead compound for the development of new drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 245728-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,7,2 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 245728-73:
(8*2)+(7*4)+(6*5)+(5*7)+(4*2)+(3*8)+(2*7)+(1*3)=158
158 % 10 = 8
So 245728-73-8 is a valid CAS Registry Number.
245728-73-8Relevant articles and documents
Stereoselective chemoenzymatic synthesis of both enantiomers of protected 4-amino-2-pentanone
Besse, Pascale,Ciblat, Stephane,Canet, Jean-Louis,Troin, Yves,Veschambre, Henri
, p. 2213 - 2224 (1999)
An acetal protected 4-amino-2-pentanone was synthesised by two different routes in 10 and seven steps, respectively, the key step being a microbiological reduction. Both enantiomers of the amine were obtained enantiomerically pure.
Synthesis and in vitro sodium channel blocking activity evaluation of novel homochiral mexiletine analogs
Carocci, Alessia,Catalano, Alessia,Bruno, Claudio,Lentini, Giovanni,Franchini, Carlo,De Bellis, Michela,De Luca, Annamaria,Camerino, Diana Conte
scheme or table, p. 299 - 307 (2010/10/21)
New chiral mexiletine analogs were synthesized in their optically active forms and evaluated in vitro as use-dependent blockers of skeletal muscle sodium channels. Tests carried out on sodium currents of single muscle fibers of Rana esculenta demonstrated
