16595-76-9 Usage
Uses
Used in Pharmaceutical Research and Development:
(R)-2,3,5,6-tetrahydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride is used as a compound in pharmaceutical research and development for its potential pharmacological activity. (R)-2,3,5,6-tetrahydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride is being studied for its possible applications in various medical fields, making it a valuable asset in the search for new therapeutic agents.
Used in Drug Design and Synthesis:
In the field of drug design and synthesis, (R)-2,3,5,6-tetrahydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride serves as a key building block or intermediate for the development of novel pharmaceuticals. Its unique chemical structure allows for the creation of new drugs with potentially improved efficacy and reduced side effects.
Used in Medicinal Chemistry:
(R)-2,3,5,6-tetrahydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride is used as a starting material or a structural component in medicinal chemistry. Its incorporation into various drug candidates can lead to the discovery of new therapeutic agents with specific targeting capabilities, enhancing the treatment options for various medical conditions.
Used in Drug Delivery Systems:
(R)-2,3,5,6-tetrahydro-6-phenylimidazo[2,1-b]thiazole monohydrochloride can be employed in the development of innovative drug delivery systems. These systems aim to improve the bioavailability, targeting, and overall efficacy of the compound, ensuring that it reaches the intended site of action within the body and minimizes potential side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 16595-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,9 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16595-76:
(7*1)+(6*6)+(5*5)+(4*9)+(3*5)+(2*7)+(1*6)=139
139 % 10 = 9
So 16595-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2S.ClH/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10;/h1-5,10H,6-8H2;1H/t10-;/m0./s1
16595-76-9Relevant articles and documents
A CONVENIENT METHOD FOR OPTICAL RESOLUTIONS VIA DIASTEREOISOMERIC SALT FORMATION
Acs, M.,Fogassy, E.,Faigl, F.
, p. 2465 - 2470 (2007/10/02)
With the advantage of the method using two immiscible solvents and half-equivalent amount of the resolving agent, higher optical purity can be obtained than in cases of any other resolution via diastereoisomeric salt formation, besides it is a faster procedure for resolution of a new racemate as well.