1095565-81-3 Usage
Description
(5S)-2-[(1S,2S,4R)-Bicyclo[2.2.1]hept-2-ylamino]-5-methyl-5-(1-methylethyl)-4(5H)-thiazolone is a complex organic compound characterized by a thiazolone ring structure. It features a bicyclic heptane ring, an amino group, and a thiazolone ring, along with a methyl and isopropyl group attached to the thiazolone ring. This intricate molecular architecture positions it as a candidate for applications in medicinal chemistry and the pharmaceutical industry, pending further research into its specific properties and uses.
Uses
Used in Medicinal Chemistry:
(5S)-2-[(1S,2S,4R)-Bicyclo[2.2.1]hept-2-ylamino]-5-methyl-5-(1-methylethyl)-4(5H)-thiazolone is utilized as a compound in medicinal chemistry for its potential to contribute to the development of new drugs. Its unique structure may offer novel interactions with biological targets, which could lead to the discovery of new therapeutic agents.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (5S)-2-[(1S,2S,4R)-Bicyclo[2.2.1]hept-2-ylamino]-5-methyl-5-(1-methylethyl)-4(5H)-thiazolone is employed as a building block for the synthesis of pharmaceuticals. Its structural components may be key in the creation of new molecules with specific therapeutic effects, thus expanding the range of available treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1095565-81-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,5,5,6 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1095565-81:
(9*1)+(8*0)+(7*9)+(6*5)+(5*5)+(4*6)+(3*5)+(2*8)+(1*1)=183
183 % 10 = 3
So 1095565-81-3 is a valid CAS Registry Number.
1095565-81-3Relevant articles and documents
Asymmetric alkylation of 5-alkyl-2-aminothiazolones using a C 2-symmetric chiral tetraamine base
Frizzle, Matthew J.,Nani, Roger R.,Martinelli, Michael J.,Moniz, George A.
scheme or table, p. 5613 - 5616 (2011/11/12)
The diastereoselective alkylation of a series of 5-alkyl-2-aminothiazolones utilizing a C2-symmetric chiral tetraamine base is reported.
ASYMMETRIC PROCESS FOR MAKING SUBSTITUTED 2-AMINO-THIAZOLONES
-
Page/Page column 24-25, (2010/04/03)
The invention provides two process for synthesizing substituted aminothiazolone compounds as inhibitors of 11-β-hydroxy steroid dehydrogenase type 1. The processes allow the stereoselective synthesis of the desired compounds without the use of stoichiometric amounts of chiral catalysts.
Two asymmetric syntheses of AMG 221, an inhibitor of 11β- hydroxysteroid dehydrogenase type 1
Caille, Seb,Cui, Sheng,Hwang, Tsang-Lin,Wang, Xiang,Faul, Margaret M.
experimental part, p. 3833 - 3842 (2009/11/30)
(Chemical Equation Presented) Two asymmetric syntheses of AMG 221 (2), an inhibitor of 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) discovered in our laboratories, are reported. One of the syntheses utilizes chiral trimethylsilyl cyanohydrin 12 as s
