120155-43-3 Usage
Uses
Used in Scientific Research:
4-Thiazoleacetic acid, ethyl ester is used as a research chemical for various scientific applications. Its unique structure and properties make it a valuable compound for studying chemical reactions, synthesis, and potential interactions with other molecules. 4-Thiazoleacetic acid, ethyl ester's role in research is crucial for advancing our understanding of organic chemistry and its applications in various fields.
Used in Pharmaceutical Development:
4-Thiazoleacetic acid, ethyl ester is used as a building block or intermediate in the synthesis of pharmaceutical compounds. Its presence in the class of thiazoles suggests that it may have potential applications in the development of new drugs, particularly those targeting specific biological pathways or receptors. 4-Thiazoleacetic acid, ethyl ester's versatility in chemical reactions allows for the creation of diverse drug candidates, which can be further optimized for therapeutic efficacy and safety.
Used in Chemical Synthesis:
4-Thiazoleacetic acid, ethyl ester is used as a reagent or catalyst in various chemical synthesis processes. Its ability to participate in a range of reactions, such as substitution, addition, or elimination, makes it a valuable component in the production of other organic compounds. This versatility is particularly useful in the synthesis of complex molecules, where multiple steps and reactions are required to achieve the desired product.
Used in Material Science:
4-Thiazoleacetic acid, ethyl ester is used as a component in the development of new materials with specific properties. Its incorporation into polymers, for example, could potentially enhance their stability, reactivity, or other characteristics. This application is particularly relevant in the fields of electronics, where materials with tailored properties are needed for the development of advanced devices and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 120155-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,5 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120155-43:
(8*1)+(7*2)+(6*0)+(5*1)+(4*5)+(3*5)+(2*4)+(1*3)=73
73 % 10 = 3
So 120155-43-3 is a valid CAS Registry Number.
120155-43-3Relevant articles and documents
PYRUVATE KINASE ACTIVATORS FOR USE IN TREATING BLOOD DISORDERS
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Page/Page column 185, (2019/03/05)
Described herein are compounds that activate pyruvate kinase R, pharmaceutical compositions and methods of use thereof. These compounds are represented by Formula (I): Formula (I) wherein R', R2, L', and L2 are as defined herein.
Inhibitors of protein isoprenyl transferases
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, (2008/06/13)
Compounds having the formula or a pharmaceutically acceptable salt thereof wherein R1is (a) hydrogen, (b) loweralkyl, (c) alkenyl, (d) alkoxy, (e) thioalkoxy, (f) halo, (g) haloalkyl, (h) aryl-L2—, and (i) heterocyclic-L2—; R2is selected from (a) (b) —C(O)NH—CH(R14)—C(O)OR15, (d) —C(O)NH—CH(R14)—C(O)NHSO2R16, (e) —C(O)NH—CH(R14)-tetrazolyl, (f) —C(O)NH-heterocyclic, and (g) —C(O)NH—CH(R14)—C(O)NR17R18; R3is substituted or unsubstituted heterocyclic or aryl, substituted or unsubstituted cycloalkyl or cycloalkenyl, and —P(W)RR3RR3′; R4is hydrogen, lower alkyl, haloalkyl, halogen, aryl, arylakyl, heterocyclic, or (heterocyclic)alkyl; L1is absent or is selected from (a) —L4—N(R5)—L5—, (b) —L4—O—L5—, (c) —L4—S(O)n—L5— (d) —L4—L6—C(W)—N(R5)—L5—, (e) —L4—L6—S(O)m—N(R5)—L5—, (f) —L4—N(R5)—C(W)—L7—L5—, (g) —L4—N(R5)—S(O)p—L7—L5—, (h) optionally substituted alkylene, (i) optionally substituted alkenylene, (j) optionally substituted alkynylene (k) a covalent bond, (l) and (m) are inhibitors of protein isoprenyl transferases. Also disclosed are protein isoprenyl transferase inhibiting compositions and a method of inhibiting protein isoprenyl transferases.
2-Alkoxy(and 2-alkoxyalkyl)-2-heterocyclic-thioacetamides for inhibiting gastric acid secretion
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, (2008/06/13)
The compounds are 2-alkoxy(and 2-alkoxyalkyl)-2-heterocyclic-thioacetamides which are inhibitors of gastric acid secretion.
2-Alkoxy(and 2-amino)-3-amino-2-heterocyclic-thiopropanamides
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, (2008/06/13)
The compounds are 2-alkoxy(and 2-amino)-3-amino-2-heterocyclic-thiopropanamides, for example 2-methoxy-N-methyl-3-morpholino-2-(2-pyridyl)thiopropanamide, which are inhibitors of gastric acid secretion.
