79247-79-3 Usage
Description
Methyl 5-bromo-4-methylthiazole-2-carboxylate is a chemical compound with the molecular formula C7H7BrNO2S. It is a derivative of thiazole-2-carboxylate and contains a bromine atom and a methyl group. Methyl 5-bromo-4-methylthiazole-2-carboxylate is of interest to researchers in organic chemistry and chemical biology due to its potential applications and biological activities.
Uses
Used in Pharmaceutical Synthesis:
Methyl 5-bromo-4-methylthiazole-2-carboxylate is used as an intermediate in the synthesis of pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs with various therapeutic properties.
Used in Agrochemical Synthesis:
In addition to its pharmaceutical applications, Methyl 5-bromo-4-methylthiazole-2-carboxylate is also used as an intermediate in the synthesis of agrochemicals. This makes it a valuable compound in the development of pesticides and other agricultural products.
Used in Organic Chemistry Research:
Methyl 5-bromo-4-methylthiazole-2-carboxylate is utilized in organic chemistry research to explore its chemical properties and potential reactions. This helps scientists better understand the compound and its possible applications in various fields.
Used in Chemical Biology Research:
Due to its potential biological activities, Methyl 5-bromo-4-methylthiazole-2-carboxylate is studied in chemical biology research. Scientists are interested in its antimicrobial and antiparasitic effects, which could lead to the development of new treatments for various diseases and infections.
Used in Antimicrobial Applications:
Methyl 5-bromo-4-methylthiazole-2-carboxylate is used as an antimicrobial agent for its potential to combat various microorganisms. This application is particularly relevant in the development of new antibiotics and antifungal agents.
Used in Antiparasitic Applications:
Methyl 5-bromo-4-methylthiazole-2-carboxylate is also used in antiparasitic applications, where it may exhibit activity against parasites. This could lead to the creation of new treatments for parasitic infections and diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 79247-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,4 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79247-79:
(7*7)+(6*9)+(5*2)+(4*4)+(3*7)+(2*7)+(1*9)=173
173 % 10 = 3
So 79247-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BrNO2S/c1-3-4(7)11-5(8-3)6(9)10-2/h1-2H3
79247-79-3Relevant articles and documents
Viral polymerase inhibitors
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Page 28, (2010/02/06)
An isomer, enantiomer, diastereoisomer, or tautomer of a compound, represented by formula I: wherein R1 is selected from: H, haloalkyl, (C1-6)alkyl, (C2-6)alkenyl, (C3-7)cycloalkyl, (C2-6)alkynyl, (C5-7)cycloalkenyl, 6 or 10-membered aryl, Het all optionally substituted; R2 is selected from (C1-6)alkyl, (C3-7)cycloalkyl, (C6-10)bicycloalkyl, 6- or 10-membered aryl, or Het all optionally substituted; B is N or CR5, wherein R5 is H, halogen, haloalkyl, (C1-6)alkyl, (C3-7)cycloalkyl or (C1-6)alkyl-(C3-7)cycloalkyl; X is N or CR5; D is N or CR5; each of Y1 and Y2 is independently O or S; Z is O, N, or NRz wherein Rz is H, (C1-6)alkyl, (C3-7)cycloalkyl or (C1-6)alkyl-(C3-7)cycloalkyl; R3 and R4 are each independently H, (C1-6)alkyl, first (C3-7)cycloalkyl or 6- or 10-membered aryl, Het (C1-6)alkyl-6- or 10-membered aryl, (C1-6)alkyl-Het; or each R3 and R4 are independently covalently bonded together to form second (C3-7)cycloalkyl, or heterocycle, all optionally substituted; or when Z is N, either R3 or R4 are independently covalently bonded thereto to form a nitrogen-containing heterocycle; R7 is H, (C1-6 alkyl), (C3-7)cycloalkyl or (C1-6)alkyl-(C3-7)cycloalkyl; or R7 is covalently bonded to either of R3 or R4 to form a heterocycle; A is (C1-6) alkyl-CONHR8 wherein R8 is-6- or 10-membered aryl, or Het; or A is a 6- or 10-membered aryl, or Het said aryl or Het being optionally substituted; or a salt or a derivative thereof; such compounds being potent inhibitors of HCV NS5B polymerase.
