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The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.3581-87-1, Name is 2-Methylthiazole, molecular formula is C4H5NS. In a Article,once mentioned of 3581-87-1, Quality Control of: 2-Methylthiazole

2-Methyl-1,3-thiazole, 2,4-dimethyl-1,3-thiazole, 2,4,5-trimethyl-1,3- thiazole, 2,4,5-trimethyl-1,3-oxazole, 2-methyl-1,3-benzoxazole and 2-methyl-1,3-benzothiazole were each treated with benzoyl chloride in acetonitrile containing triethylamine to give the corresponding (Z)-2-(heterocyclic)-1-phenylvinyl benzoates. Base hydrolysis of these vinyl benzoates gave the corresponding 2-(heterocyclic)-1-phenylethenols, which exist in both keto and enol tautomeric forms. These tautomers were used as starting materials for the syntheses of fused-ring heterocycles. The reactivity of the keto-enol tautomers depends on the nature of the heteroatom and the substituents that are present on the ring. Each tautomeric pair reacts with dimethyl acetylenedicarboxylate (DMAD) in methanol to give the 5,6-ring-fused 8-benzoyl-5-oxo-5H-thiazolo- and 8-benzoyl-5-oxo-5H-oxazolopyridinecarboxylate, 4-benzoyl-1-oxo-1H-pyrido[2,1-b]benzoxazolecarboxylate and 4-benzoyl-1-oxo-1H- pyrido[2,1-b]benzothiazolecarboxylate derivatives. Two novel 5,7-ring-fused compounds, tetramethyl 9-benzoyl-2,3-dimethyl-5,6-dihydrothiazolo[3,2-a]azepine- 5,6,7,8-tetracarboxylate and its oxazole analogue, were also obtained when the tautomers formed from 2,4,5-trimethyl-1,3-thiazole and 2,4,5-trimethyl-1,3- oxazole, respectively, were treated with DMAD. Reactions of the tautomers with methyl propiolate did not, however, give satisfactory results. Georg Thieme Verlag Stuttgart. New York.

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Reference:
Thiazole | C3H3775NS – PubChem,
Thiazole | chemical compound | Britannica

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Aminopyrazine compounds as modulators of an adenosine receptor are provided. The compounds may find use as therapeutic agents for the treatment of diseases mediated through a G-protein-coupled receptor signaling pathway and may find particular use in oncology.

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Reference:
Thiazole | C3H3746NS – PubChem,
Thiazole | chemical compound | Britannica

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Nuclear magnetic resonance (NMR) spectroscopy has been established as a potent method for the determination of foldamer structures in solution. However, the NMR techniques could be limited by averaging, so additional experimental techniques are often needed to fully endorse the folding properties of a sequence. We have recently demonstrated that oligo-gamma-peptides composed of 4-amino(methyl)-1,3-thiazole-5-carboxylic acids (ATCs) adopt an original helical fold stabilized by hydrogen bonds forming C9 pseudocycles. The main objective of the present work is to reinvestigate the folding of ATC oligomer 1 in order to identify reliable FT-IR and NMR structural markers that are of value for tracking the degree of organization of ATC-based peptides.

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Reference:
Thiazole | C3H3714NS – PubChem,
Thiazole | chemical compound | Britannica

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Provided herein are PAK inhibitors and methods of utilizing PAK inhibitors for the treatment of cell proliferative disorders and/or CNS disorders.

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Thiazole | C3H3704NS – PubChem,
Thiazole | chemical compound | Britannica

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The invention relates to a compound of formula (I) wherein R1 and R2 are defined as in the description and in the claims. The compound of formula (I) can be used as a medicament against diabetes, atherosclerosis and other conditions linked to cathepsin.

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Reference:
Thiazole | C3H3682NS – PubChem,
Thiazole | chemical compound | Britannica

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[Problem] high carrier mobility, heat resistance and having a novel organic semiconductor having solvent solubility, the organic semiconductor film comprises a composition, a composition for film-making a film using an organic thin film, and the organic thin film transistor element in an active layer. (1) represented by the general formula [a][1 a](In the formula, R1 And R2 Is, independently, a hydrogen atom, an alkyl group of 1 – 20 carbon atoms, the carbon number of 1 – 20 of the haloalkyl group, or alkyl group of carbon number 1 – 12 6 – 14 carbon atoms of the aromatic hydrocarbon group may be substituted. ) [jichiazorobenzojichiohuen[jichiazorobenzojichiohuen] compound represented[Drawing] no (by machine translation)

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Reference:
Thiazole | C3H3778NS – PubChem,
Thiazole | chemical compound | Britannica

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To follow volatile flavour release in the expired air of people during eating, several physiological and analytical constraints must be observed to obtain good quality data. An interface has been developed to sample air from the nose and ionise the volatile compounds contained therein by atmospheric pressure chemical ionisation. The ions formed are detected in a quadrupole mass spectrometer. The interface design overcomes many of the constraints and allows volatile detection in the 100-10 ppbv range, depending on the nature of the volatile compound to be analysed. The principles and operating parameters of the interface are described. Control of the ionisation process is effected through the operating conditions within the interface. Since many compounds are introduced simultaneously into the interface, it is preferable to minimise fragmentation otherwise the spectra are extremely complex and it is difficult to assign ions to compounds unequivocally, with the result that quantification is imprecise. The ionisation parameters are set to favour formation of the protonated molecular (MH+) ion from the compounds and minimise formation of cluster ions, which can also confuse the spectra. The sensitivity and linearity of the technique is demonstrated for a range of flavour volatiles with a dynamic range of three orders of magnitude. The lower limit of sensitivity is determined by the signal to noise ratio whereas the upper limit occurs when all the available charge is exhausted. The technique was designed primarily to monitor real-time changes in the concentration of known volatiles during eating and has limited identification power. However, for reliable quantification, it is necessary to assign the ions monitored in-nose with the volatile compounds present in the food. Besides assignments made on nominal mass, isotopic ratio analysis and accurate mass measurements have also been used to determine the contribution of certain compounds to a particular ion intensity. Copyright (C) 2000 Elsevier Science Ltd.

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Reference:
Thiazole | C3H3635NS – PubChem,
Thiazole | chemical compound | Britannica

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Discrimination between defective and non-defective Brazilian coffee beans by their volatile profile

The coffee roasted in Brazil is considered to be of low quality, due to the presence of defective coffee beans that depreciate the beverage quality. In view of the fact that coffee flavour is directly related to the volatile compounds produced during roasting, the objective of the present study was to perform a comparative evaluation of the volatile fraction of defective (black, immature, sour) and healthy coffee beans, in order to find possible chemical markers for detection of defective coffee beans in roasted coffee. Volatiles extraction and concentration was performed by solid phase micro-extraction (SPME) of the roasted coffee headspace, using a triple phase (divinylbenzene/carboxen/polydimethylsiloxane) fiber. Analysis of the volatile profiles was performed by GC-MS. The results obtained showed that the proposed methodology was adequate for extraction, concentration and analysis of the coffees volatile profile. Several substances were identified as possible markers for differentiating black, sour and immature beans from healthy coffee beans. Statistical analysis of the data by principal components (PCA) demonstrated that the volatile profile enables the differentiation of healthy and defective coffees. The data were separated into two major groups, one represented by immature and black beans and the other by healthy and sour coffee beans. Such results indicated that black and sour beans can be associated to fermentation of immature and of healthy beans, respectively.

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Thiazole | C3H3694NS – PubChem,
Thiazole | chemical compound | Britannica

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Chemotherapeutic nitroheterocycles. Antischistosomal properties of nitrofurylvinyl and nitrothienylvinyl heterocycles

A series of 24 analogs of the experimental antischistosomal agent, 5 amino 3 [2 (5 nitro 2 furyl) vinyl] 1,2,4 oxadiazole, was prepared and evaluated in mice infected with Schistosoma mansoni. Although antischistosomal activity was widespread in the series, only four of the compounds showed significant curative properties. Compounds containing 2 imidazolyl and 2 pyridyl groups gave cure rates around 25% at 400 and 250 mg/kg dose levels, respectively. The 2 thiazolyl and 2 pyrimidyl derivatives were especially notable, yielding 100% cures at 250 and 200 mg/kg dose levels, respectively.

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Reference:
Thiazole | C3H3754NS – PubChem,
Thiazole | chemical compound | Britannica

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FAAH INHIBITORS

The present disclosure relates to compounds useful as inhibitors of the enzyme Fatty Acid Amide Hydrolase (FAAH). The disclosure also provides pharmaceutically acceptable compositions comprising the compounds of the disclosure and methods of using the compositions in the treatment or prevention of various disorders. Compounds of the invention are represtented by one of Formula A or Formula B

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Reference:
Thiazole | C3H3669NS – PubChem,
Thiazole | chemical compound | Britannica