90437-72-2 Usage
Description
4-METHYL-2-MORPHOLIN-4-YL-1,3-THIAZOLE-5-CARBALDEHYDE is a chemical compound with a molecular formula C11H14N2OS. It is a thiazole derivative containing a morpholine ring and a carbonyl group. 4-METHYL-2-MORPHOLIN-4-YL-1,3-THIAZOLE-5-CARBALDEHYDE has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. It may also have industrial uses as a reagent or intermediate in the synthesis of other organic compounds. Its specific properties and potential uses would need to be further investigated through research and testing.
Uses
Used in Pharmaceutical Development:
4-METHYL-2-MORPHOLIN-4-YL-1,3-THIAZOLE-5-CARBALDEHYDE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure, including the thiazole and morpholine rings, may contribute to the development of new drugs with specific therapeutic properties.
Used in Medicinal Chemistry Research:
As a thiazole derivative, 4-METHYL-2-MORPHOLIN-4-YL-1,3-THIAZOLE-5-CARBALDEHYDE is used in medicinal chemistry research to explore its potential as a lead compound for drug discovery. Its chemical properties and interactions with biological targets can be studied to identify possible applications in treating various diseases and conditions.
Used in Organic Synthesis:
4-METHYL-2-MORPHOLIN-4-YL-1,3-THIAZOLE-5-CARBALDEHYDE is used as a reagent or intermediate in the synthesis of other organic compounds. Its carbonyl group can participate in various chemical reactions, making it a valuable component in the preparation of complex organic molecules for different industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Chemical Industry:
In the chemical industry, 4-METHYL-2-MORPHOLIN-4-YL-1,3-THIAZOLE-5-CARBALDEHYDE may be utilized as a building block for the creation of novel compounds with specific applications. Its versatility in chemical reactions allows for the development of new products with potential uses in various sectors, such as coatings, adhesives, and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 90437-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,3 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90437-72:
(7*9)+(6*0)+(5*4)+(4*3)+(3*7)+(2*7)+(1*2)=132
132 % 10 = 2
So 90437-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O2S/c1-7-8(6-12)14-9(10-7)11-2-4-13-5-3-11/h6H,2-5H2,1H3
90437-72-2Relevant articles and documents
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.