90916-45-3 Usage
Uses
Used in Pharmaceutical Research:
C-(4-Phenyl-thiazol-2-yl)-methylamine is utilized as a key intermediate in the synthesis of biologically active molecules, particularly for drug discovery and development. Its unique structure and properties make it a valuable component in the creation of new pharmaceuticals.
Used in Central Nervous System Disorders:
In the field of medicine, C-(4-Phenyl-thiazol-2-yl)-methylamine is employed as a precursor for the development of drugs targeting central nervous system disorders. Its potential applications in this area highlight its importance in advancing treatments for neurological conditions.
Used in Organic Synthesis:
Beyond its medicinal applications, C-(4-Phenyl-thiazol-2-yl)-methylamine also serves as a reagent in organic synthesis. It is used for the preparation of a diverse range of organic compounds, contributing to the broader field of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 90916-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,1 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90916-45:
(7*9)+(6*0)+(5*9)+(4*1)+(3*6)+(2*4)+(1*5)=143
143 % 10 = 3
So 90916-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2S/c11-6-10-12-9(7-13-10)8-4-2-1-3-5-8/h1-5,7H,6,11H2
90916-45-3Relevant academic research and scientific papers
COMPOUNDS AND METHODS for the inhibition of HDAC
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, (2015/11/24)
Disclosed are compounds having the formula: wherein X1, X2, X3, R1, R2, R3, R4, Y, A, Z, L and n are as defined herein, and methods of making and using the same.
Synthesis and antiplasmodial activity of new heteroaryl derivatives of 7-chloro-4-aminoquinoline
Casagrande, Manolo,Barteselli, Anna,Basilico, Nicoletta,Parapini, Silvia,Taramelli, Donatella,Sparatore, Anna
, p. 5965 - 5979 (2012/10/29)
With the aim to investigate the effect of different heterocyclic rings linked to the 4-aminoquinoline nucleus on the antimalarial activity, a set of 7-chloro-N-(heteroaryl)-methyl-4-aminoquinoline and 7-chloro-N-(heteroaryl)-4- aminoquinoline was synthesi
