141034-15-3 Usage
Description
(1R,2R)-1-(4,5-dihydro-1,3-thiazol-2-ylamino)tetralin-2-ol is a chiral chemical compound characterized by a complex structure that features a thiazole ring and a tetralin ring. (1R,2R)-1-(4,5-dihydro-1,3-thiazol-2-ylamino)tetralin-2-ol is distinguished by the presence of two asymmetric carbons, a hydroxyl group, an amino group, and the thiazole ring. These structural elements suggest its potential use as a pharmaceutical or bioactive molecule, with possible applications in medicinal chemistry due to the prevalence of thiazoles in numerous bioactive compounds. (1R,2R)-1-(4,5-dihydro-1,3-thiazol-2-ylamino)tetralin-2-ol's stereochemistry and the strategic positioning of its functional groups may enable specific interactions with biological targets, although further research is required to explore its full potential and properties.
Uses
Used in Pharmaceutical Industry:
(1R,2R)-1-(4,5-dihydro-1,3-thiazol-2-ylamino)tetralin-2-ol is used as a potential pharmaceutical or bioactive molecule for its unique structural features, including the thiazole ring and the presence of hydroxyl and amino groups. These characteristics may allow the compound to interact with biological targets in ways that could be beneficial for the development of new drugs or therapies.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (1R,2R)-1-(4,5-dihydro-1,3-thiazol-2-ylamino)tetralin-2-ol serves as a subject of study for its potential applications in the design and synthesis of new bioactive compounds. (1R,2R)-1-(4,5-dihydro-1,3-thiazol-2-ylamino)tetralin-2-ol's structural elements, particularly the thiazole ring, make it an interesting candidate for further exploration and development in creating molecules with specific biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 141034-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,3 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141034-15:
(8*1)+(7*4)+(6*1)+(5*0)+(4*3)+(3*4)+(2*1)+(1*5)=73
73 % 10 = 3
So 141034-15-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N2OS/c16-11-6-5-9-3-1-2-4-10(9)12(11)15-13-14-7-8-17-13/h1-4,11-12,16H,5-8H2,(H,14,15)/t11-,12-/m1/s1
141034-15-3Relevant articles and documents
SYNTHESIS OF trans-2-IMINOTHIAZOLIDINE AND RELATED COMPOUNDS - A NEW CLASS OF ANTIDEPRESSANTS
Shukla, Upendra K.,Singh, Raieshwar,Khanna, J. M.,Saxena, Anil K.,Singh, Hemant K.,et al.
, p. 415 - 424 (2007/10/02)
Antiparasitic and antidepressant activities exhibited by tetramisole (I) and its enantiomers prompted the study of its structural analogs trans-2-iminothiazolidine (VIII/IX) and 2,3,4a,5,6,10b-hexahydronaphthoimidazothiazole (XII), 2,3,4a,5-tetrahydro-9bH-indenoimidazothiazole (XIII), and 2,3,4a,5-tetrahydro-9bH-indenoimidazothiazole (XVI), and a homolog 3,4,6,7-tetrahydro-7-phenyl-2H-imidazo-1,3-thiazine (XX).While none of these compounds showed any noteworthy antiparasitic activity, the trans-2-iminothiazolidine (VIII) has shown marked antidepressant activity, better than imipramine in the tests used, and provides a new structural lead for antidepressants.
