78502-79-1 Usage
Uses
Used in Organic Synthesis:
2-(bromomethyl)-4-phenylthiazole is used as a building block in organic synthesis for the creation of a variety of biologically active molecules, leveraging its unique structural features to enhance the properties of synthesized compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(bromomethyl)-4-phenylthiazole is utilized as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs with improved therapeutic profiles.
Used in Agrochemicals:
2-(bromomethyl)-4-phenylthiazole is employed as a precursor in the synthesis of agrochemicals, potentially leading to the development of novel pesticides or other agricultural chemicals that can enhance crop protection and yield.
Used in Antimicrobial Applications:
2-(bromomethyl)-4-phenylthiazole is used as an antimicrobial agent due to its demonstrated properties against certain microorganisms, offering a potential alternative or supplement to existing treatments in the field of infectious diseases.
Used in Antifungal Applications:
2-(bromomethyl)-4-phenylthiazole is utilized as an antifungal agent, highlighting its potential in combating fungal infections, which is crucial in both medical and agricultural settings.
Used in Cancer Therapy Research:
In cancer therapy, 2-(bromomethyl)-4-phenylthiazole is studied for its potential application in treating cancer, with ongoing research exploring its mechanisms of action and efficacy in inhibiting tumor growth and progression.
Used in Different Industries:
2-(bromomethyl)-4-phenylthiazole finds applications across various industries, including pharmaceuticals, agriculture, and medical research, where it serves as a versatile chemical intermediate and active compound for the development of innovative products and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 78502-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,0 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78502-79:
(7*7)+(6*8)+(5*5)+(4*0)+(3*2)+(2*7)+(1*9)=151
151 % 10 = 1
So 78502-79-1 is a valid CAS Registry Number.
78502-79-1Relevant academic research and scientific papers
Novel oxime derivative as well as preparation method and application thereof
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Paragraph 0134-0135; 0138-0139, (2021/06/22)
The invention relates to a novel oxime derivative and a preparation method and application thereof, the novel oxime derivative has a structure as shown in formula (I), Q is optionally substituted phenyl, T is C1-6 alkyl substituted tetrazolyl, and A is th
IMIDAZOTHIADIAZOLE AND IMIDAZOPYRAZINE DERIVATIVES AS PROTEASE ACTIVATED RECEPTOR 4 (PAR4) INHIBITORS FOR TREATING PLATELET AGGREGATION
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Paragraph 00150, (2013/11/18)
The present invention provides thiazole compounds of Formula I wherein W, Y, R0, R2, R4, R5, R6, R7, X1, X2, X3 and X4 are as defined herein, or a stereoisomer, tautomer, pharmaceutically acceptable salt, prodrug ester or solvate form thereof, wherein all of the variables are as defined herein. These compounds are inhibitors of platelet aggregation and thus can be used as medicaments for treating or preventing thromboembolic disorders.
PAR4 AGONIST PEPTIDES
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Page/Page column, (2013/11/06)
The present invention provides PAR4 agonist peptides. These peptides are useful for developing robust PAR4 receptor assays.
N-Bromosuccinimide Bromination of Substituted Methylthiazoles
Krieg, Benno,Mittner, Juergen
, p. 623 - 632 (2007/10/02)
Bromination of methylthiazoles with one unsubstituted position by N-bromosuccinimide may take place either at the methyl group, at the heterocyclic nucleus, or at both positions according to the nature of the second substituent.The ethoxycarbonyl group in the compounds 1a-3a directs the bromine into the side chain.So it is possible to obtain the tribromomethyl compounds 1d and 2d without bromination of the thiazole nucleus.In the phenyl-substituted methylthiazoles 4a-6a bromination takes place in the methyl group and in the heterocyclic nucleus. - The bromomethylthiazoles 1b-3b yield the vinylthiazoles 1k-3k by Wittig reaction.
