92940-24-4 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Diethylamino-thiazole-5-carbaldehyde is used as a reagent for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, 2-Diethylamino-thiazole-5-carbaldehyde is utilized as a reagent in the synthesis of various agrochemicals, potentially aiding in the creation of pesticides and other agricultural products.
Used in Dye Manufacturing:
2-DIETHYLAMINO-THIAZOLE-5-CARBALDEHYDE is also employed in the production of dyes, where it serves as a reagent to develop a spectrum of colorants for different applications.
Used as a Fluorescence Marker in Biochemistry:
2-Diethylamino-thiazole-5-carbaldehyde is used as a fluorescence marker in biochemical research, particularly for studying protein folding and enzyme activity, providing insights into biological processes and mechanisms.
Used in the Preparation of Thiazole-based Compounds:
As a key intermediate, 2-Diethylamino-thiazole-5-carbaldehyde is instrumental in the preparation of various thiazole-based compounds, which are used across different industries for their unique properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 92940-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,4 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92940-24:
(7*9)+(6*2)+(5*9)+(4*4)+(3*0)+(2*2)+(1*4)=144
144 % 10 = 4
So 92940-24-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2OS/c1-3-10(4-2)8-9-5-7(6-11)12-8/h5-6H,3-4H2,1-2H3
92940-24-4Relevant academic research and scientific papers
Synthesis of nonlinear optical chromophores containing electron-excessive and -deficient heterocyclic bridges. The auxiliary donor-acceptor effects
Shu, Ching-Fong,Wang, Yuh-Kai
, p. 833 - 835 (2007/10/03)
Push-pull substituted nonlinear optical chromophores with thiazole and thiophene rings and interposed ethylene units as π-conjugated bridges were synthesized. The effects of the nature and location of the heterocycles on the energy of the charge transfer transition for the chromophores are discussed.
An Easy General Synthesis of 2-(N,N-Dialkylamino)thiazol-5-yl Aldehydes and Ketones
Sawhney, Indu,Wilson, John R. H.
, p. 329 - 331 (2007/10/02)
Reaction between 2-chloro-5-thiazolyl-lithium and N,N-dialkylformamides or amides gave 2-N,N-dialkylaminothiazol-5-yl aldehydes or ketones on quenching with water.Quenching with acid gave 2-chlorothiazole-5-yl aldehydes or ketones, from which chloride was easily displaced by free amines.
