52829-53-5 Usage
Uses
Used in Medicinal Chemistry and Pharmaceutical Research:
4-(Bromomethyl)-1,3-thiazole is used as a precursor for the development of new drug compounds. Its unique structure and functional groups make it a valuable building block in the synthesis of pharmaceuticals with potential therapeutic applications.
Used in Agrochemical Production:
4-(BROMOMETHYL)-1,3-THIAZOLE is utilized in the production of agrochemicals, where it can contribute to the development of new pesticides, herbicides, and other agricultural chemicals to improve crop protection and yield.
Used in Dye and Specialty Chemicals Manufacturing:
4-(Bromomethyl)-1,3-thiazole is used as a key intermediate in the synthesis of dyes and specialty chemicals, which find applications in various industries such as textiles, plastics, and coatings.
Used in Materials Science:
4-(BROMOMETHYL)-1,3-THIAZOLE has potential applications in materials science, where it can be incorporated into the development of new materials with unique properties, such as improved conductivity, stability, or reactivity.
Used as a Reagent in Organic Synthesis:
4-(Bromomethyl)-1,3-thiazole serves as a reagent in organic synthesis, enabling chemists to perform various chemical reactions and transformations, leading to the formation of new compounds with desired properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 52829-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,2 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52829-53:
(7*5)+(6*2)+(5*8)+(4*2)+(3*9)+(2*5)+(1*3)=135
135 % 10 = 5
So 52829-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H4BrNS/c5-1-4-2-7-3-6-4/h2-3H,1H2
52829-53-5Relevant academic research and scientific papers
Anthranilic acid derivatives as inhibitors of the cGMP-phosphodiesterase
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, (2008/06/13)
Compounds of formula (I) STR1where R 1 is hydrogen; R 2 is nitro, cyano or halo(lower)alkyl; R 3 is phenyl substituted with one or more substituents selected from halogen, cyano and lower alkoxy; A is a lower alkylene group; R 4 is a group CR 6 R 7 R 8 wherein R 6 and R 7 form, together with the carbon atom to which they are attached a cycloalkyl group optionally substituted with hydroxy, lower alkoxy or a lower alkanoylamino; and R 8 is hydrogen; its prodrug and a salt thereof.
