141034-13-1 Usage
Description
(2-hydroxytetralin-1-yl)thiourea is a chemical compound with the molecular formula C13H15NOS. It is a thiourea derivative containing a tetralin ring with a hydroxy group attached to it. Thiourea compounds are known for their diverse biological and pharmacological activities, and (2-hydroxytetralin-1-yl)thiourea is no exception. It has been studied for its potential as a drug candidate, particularly in the field of medicinal chemistry. Its specific properties and potential applications would require further research and investigation.
Uses
Used in Pharmaceutical Industry:
(2-hydroxytetralin-1-yl)thiourea is used as a drug candidate for its potential biological and pharmacological activities. Its unique structure and properties make it a promising candidate for the development of new therapeutic agents.
Used in Medicinal Chemistry Research:
(2-hydroxytetralin-1-yl)thiourea is used as a subject of study in medicinal chemistry research to explore its potential applications and properties. Further research and investigation are needed to fully understand its capabilities and potential uses in the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 141034-13-1 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 141034-13:
(8*1)+(7*4)+(6*1)+(5*0)+(4*3)+(3*4)+(2*1)+(1*3)=71
71 % 10 = 1
So 141034-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2OS/c12-11(15)13-10-8-4-2-1-3-7(8)5-6-9(10)14/h1-4,9-10,14H,5-6H2,(H3,12,13,15)
141034-13-1Relevant 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.
