623143-42-0 Usage
Description
(S)-1-(thiazol-2-yl)ethanamine hydrochloride is a chemical compound that belongs to the class of organic compounds known as thiazoles. These are aromatic heterocyclic compounds characterized by a five-member ring composed of one sulfur atom, one nitrogen atom, and three carbon atoms. The hydrochloride salt form of this compound typically enhances its solubility in water. Although its direct biological role or effects may not be fully established, it is often explored for potential pharmaceutical or industrial applications. As with all chemicals, it is essential to handle (S)-1-(thiazol-2-yl)ethanamine hydrochloride with appropriate safety measures.
Uses
Used in Pharmaceutical Industry:
(S)-1-(thiazol-2-yl)ethanamine hydrochloride is used as a potential pharmaceutical compound for its exploration in drug development. Its unique chemical structure may offer opportunities for the creation of new therapeutic agents, particularly in the context of medicinal chemistry.
Used in Chemical Research:
In the field of chemical research, (S)-1-(thiazol-2-yl)ethanamine hydrochloride serves as a subject of study for understanding the properties and reactivity of thiazoles. This can contribute to the advancement of synthetic chemistry and the discovery of new chemical reactions or processes.
Used in Material Science:
(S)-1-(thiazol-2-yl)ethanamine hydrochloride may be utilized in material science applications, where its properties could be harnessed to develop new materials with specific characteristics, such as improved solubility or reactivity in certain conditions.
Used in Industrial Applications:
Although specific uses may not be fully established, (S)-1-(thiazol-2-yl)ethanamine hydrochloride could be explored for potential industrial applications, such as in the synthesis of other compounds or as an intermediate in the production of various chemical products. Its solubility and reactivity may be advantageous in certain industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 623143-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,1,4 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 623143-42:
(8*6)+(7*2)+(6*3)+(5*1)+(4*4)+(3*3)+(2*4)+(1*2)=120
120 % 10 = 0
So 623143-42-0 is a valid CAS Registry Number.
623143-42-0Relevant articles and documents
Transaminases applied to the synthesis of high added-value enantiopure amines
Paul, Caroline E.,Rodriguez-Mata, Maria,Busto, Eduardo,Lavandera, Ivan,Gotor-Fernandez, Vicente,Gotor, Vicente,Garcia-Cerrada, Susana,Mendiola, Javier,De Frutos, Oscar,Collado, Ivan
supporting information, p. 788 - 792 (2014/07/08)
Critical parameters affecting the stereoselective amination of (hetero)aromatic ketones using transaminases have been studied, such as temperature, pH, substrate concentration, cosolvent, and source and percentage of amino donor, to further optimize the production of enantiopure amines using both (S)- and (R)-selective biocatalysts from commercial suppliers. Interesting enantiopure amino building blocks have been obtained, overcoming some limitations of traditional chemical synthetic methods. Representative processes were scaled up, affording halogenated and heteroaromatic amines in enantiomerically pure form and good isolated yields.
PYRAZOLE DERIVATIVES AS INHIBITORS OF RECEPTOR TYROSYNE KINASES
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Page/Page column 105, (2008/06/13)
Compounds of formula (I): and their use in the inhibition of Trk activity are described.
