934236-32-5 Usage
Uses
Used in Pharmaceutical Industry:
2,5-DIBROMO-4-(HYDROXYMETHYL)THIAZOLE is used as a building block for the synthesis of new drugs, leveraging its antimicrobial and antifungal properties to combat various infections and diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 2,5-DIBROMO-4-(HYDROXYMETHYL)THIAZOLE is utilized as a key component in the development of pesticides, contributing to its effectiveness against harmful microbes and fungi that can damage crops.
Used in Dye Synthesis:
2,5-DIBROMO-4-(HYDROXYMETHYL)THIAZOLE is employed as a precursor in the synthesis of fluorescent dyes, capitalizing on its chemical structure to create dyes with specific optical properties for various applications.
Used in Organic Synthesis as a Reagent:
As a reagent in organic synthesis, 2,5-DIBROMO-4-(HYDROXYMETHYL)THIAZOLE is used to facilitate specific chemical reactions, taking advantage of its unique functional groups to achieve desired outcomes in the synthesis of complex organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 934236-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,2,3 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 934236-32:
(8*9)+(7*3)+(6*4)+(5*2)+(4*3)+(3*6)+(2*3)+(1*2)=165
165 % 10 = 5
So 934236-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H3Br2NOS/c5-3-2(1-8)7-4(6)9-3/h8H,1H2
934236-32-5Relevant academic research and scientific papers
CARBAMATE, ESTER, AND KETONE COMPOUNDS FOR TREATMENT OF IMMUNE AND INFLAMMATORY DISORDERS
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Paragraph 0535, (2017/03/14)
Compounds, methods of use, and processes for making inhibitors of complement Factor D are provided comprising Formula I, I" and I'" or a pharmaceutically acceptable salt or composition thereof. The inhibitors described herein target Factor D and inhibit or regulate the complement cascade. The inhibitors of Factor D described herein reduce the excessive activation of complement.
Synthesis of 2,4,5-trisubstituted thiazoles with a 5-(N,N-dimethylaminomethyl) substituent
Stump, Bernhard,Kohler, Philipp C.,Schweizer, W. Bernd,Diederich, Francois
, p. 293 - 326 (2008/03/12)
We report synthetic strategies to 2,4,5-tri substituted thiazoles with a N,N- dimethylaminomethyl residue at C(5). Three different routes to build up these scaffolds are described. Furthermore, we report a retro-Brook rearrangement of a thiazole derivative as well as an unusual cyclization leading to a highly substituted benzothiazole.
