81569-46-2 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 2-bromo-5-ethyl-1,3-thiazole-4-carboxylate serves as a key building block in the synthesis of complex molecules for pharmaceutical applications. Its unique structure and reactivity allow for the creation of new drugs with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 2-bromo-5-ethyl-1,3-thiazole-4-carboxylate is utilized as an intermediate in the development of novel agrochemicals. Its ability to form various derivatives makes it a versatile component in the synthesis of pesticides, herbicides, and other agricultural chemicals, enhancing crop protection and yield.
Used in Materials Science:
Methyl 2-bromo-5-ethyl-1,3-thiazole-4-carboxylate also finds application in materials science, where it can be incorporated into the design and synthesis of new materials with specific properties. Its use in this field may lead to the development of innovative materials with applications in various industries, such as electronics, textiles, and coatings.
Overall, the diverse applications of Methyl 2-bromo-5-ethyl-1,3-thiazole-4-carboxylate highlight its significance as a synthetic intermediate in multiple industries, driving innovation and progress in the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 81569-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,6 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81569-46:
(7*8)+(6*1)+(5*5)+(4*6)+(3*9)+(2*4)+(1*6)=152
152 % 10 = 2
So 81569-46-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8BrNO2S/c1-3-4-5(6(10)11-2)9-7(8)12-4/h3H2,1-2H3
81569-46-2Relevant academic research and scientific papers
NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS
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Page/Page column 40, (2010/03/02)
Nitrogen-containing heterocyclic compounds represented by the following Formula (1) are provided. The compounds or salts thereof have a strong EP1 antagonistic activity when they are administered to a human or an animal, and they are useful as an effective component of a pharmaceutical agent for prophylaxis and/or treatment of an overactive bladder, for example. Furthermore, they are useful as an effective component of a pharmaceutical agent for the prophylaxis and/or treatment of symptoms including frequent urination, urinary urgency and urinary incontinence.
The Preparation of Thiazole-4- and -5-carboxylates, and an Infrared Study of their Rotational Isomers
Barton, Anne,Breukelman, Stephen P.,Kaye, Perry T.,Meakins, G. Denis,Morgan, David J.
, p. 159 - 164 (2007/10/02)
Convenient general procedures have been developed for preparing series of thiazole-4- and -5-carboxylates containing alkyl and halogeno substituents.While both series of esters show i.r. carbonyl doublets caused by rotational isomerism, the more intense absorptions of the 4-carboxylates are the lower wavenumber components, whereas those of the 5-carboxylates are the higher wavenumber components.In both series the stronger bands arise from the thermochemically more stable forms; identification of these forms as the carbonyl O,S-syn-s-trans rotamers is more certain with the 4-carboxylates than with the 5-carboxylates.
