Tag: M.W:200-300

16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 16112-21-3, Formula: C14H11NS

The cyclocondensation of 2-aminothiophenol and aldehydes has been carried out in dichloromethane using bakers’ yeast as a catalyst for obtaining 2-aryl/heteryl benzothiazoles in good yields.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Formula: C14H11NS. In my other articles, you can also check out more blogs about 16112-21-3

Reference：
Thiazole | C3H660NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 80945-86-4, Name is 6-Bromo-2-chlorobenzothiazole, molecular formula is C7H3BrClNS. In a Patent，once mentioned of 80945-86-4, Quality Control of: 6-Bromo-2-chlorobenzothiazole

Disclosed is a process for the preparation of Ethyl 4-methyl-2-(4-(2-methylpropyloxy)-3-cyanophenyl)-5-thiazolecarboxylate (I) the key intermediate for the preparation of [2-[3-cyano-4-(2-Methyl-propoxy)phenyl]-4-methyl-5-thiazole carboxylic acid (Febuxostat, I(A)) is approved under the trademark Uloric by the US Food and Drug Administration for the treatment of hyperuricemia and gouty arthritis.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Quality Control of: 6-Bromo-2-chlorobenzothiazole. In my other articles, you can also check out more blogs about 80945-86-4

Reference：
Thiazole | C3H10917NS – PubChem,
Thiazole | chemical compound | Britannica

Application of 61296-22-8, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 61296-22-8, Name is 2-Amino-5-bromothiazole monohydrobromide, molecular formula is C3H4Br2N2S. In a Patent，once mentioned of 61296-22-8

A compound of the formula: and pharmaceutical compositions for the treatment of diabetes.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 61296-22-8 is helpful to your research., Application of 61296-22-8

Reference：
Thiazole | C3H2127NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 911466-96-1, Name is 2-(Ethoxycarbonyl)thiazole-4-carboxylic acid, molecular formula is C7H7NO4S. In a Patent，once mentioned of 911466-96-1, name: 2-(Ethoxycarbonyl)thiazole-4-carboxylic acid

The present invention comprises compounds of Formula I.wherein: X, A1, A2, A3, A4, R1, R2, and R3 are defined in the specification. The invention also comprises a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is rheumatoid arthritis or psoriasis. The invention also comprises a method of modulating RORgammat activity in a mammal by administration of a therapeutically effective amount of at least one compound of claim 1.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.name: 2-(Ethoxycarbonyl)thiazole-4-carboxylic acid. In my other articles, you can also check out more blogs about 911466-96-1

Reference：
Thiazole | C3H973NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 566169-93-5, Name is 2-(4-(Methylamino)phenyl)benzo[d]thiazol-6-ol, molecular formula is C14H12N2OS. In a Patent，once mentioned of 566169-93-5, Safety of 2-(4-(Methylamino)phenyl)benzo[d]thiazol-6-ol

The present invention is directed to a method of using radiolabeled ethylene glycol (n = 1) (EG) or polyethylene glycol (n = from 2 to 10) (PEG) as a labeling group moiety on compounds that can be useful for imaging tissues. Specifically, the EG or PEG moiety preferably contains a radiofluorine (18F), and is covalently bonded to a ligand (L). The L portion of the molecule can be any molecule appropriate for covalently bonding with the radiolabeled EG or PEG moiety and subsequent use as an imaging agent. In particular, the imaging agent is preferably an agent suitable for administering to a mammal and detecting by PET or SPECT imaging.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.Safety of 2-(4-(Methylamino)phenyl)benzo[d]thiazol-6-ol, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 566169-93-5, in my other articles.

Reference：
Thiazole | C3H441NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 92-36-4, Name is 2-(4-Aminophenyl)-6-methylbenzothiazole, molecular formula is C14H12N2S. In a Patent，once mentioned of 92-36-4, Product Details of 92-36-4

Described are amino substituted hydroxyphenyl benzophenone derivatives of formula (I), wherein R1, and R2 independently from each other are; C1,-C20alkyl; C2-C20alkenyl; C3-C10,cycloalkyl; C3-C10cycloalkenyl; or R1, and R2 together with the linking nitogen atom form a 5- or 6-membered heterocyclic ring; n1 is a number from 1 to 4; when n1=1, R3 is a saturated or unsaturated heterocyclic radical; hydroxy-C1-C5alkyl; cyclohexyl optionally substituted with one or more C1,-C5alkyl; phenyl optionally substituted with a heterocyclic radical, aminocarbonyl or C1-C5alkylcarboxy; wenn n1 is 2, R3 is an alkylene-, cycloalkylene- or alkenylene radical which is optionally substituted by a carbonyl- or carboxy group; o R3 together with A forms a bivalent radical of the formula (Ia), wherein n2 is a number from 1 to 3; when n1 is 3, R3 is an alkanetriyl radical; wenn n1 is 4, R3 is an alkanetetrayl radical; A is -O-; or -N(R5)-; and R5 is hydrogen; C1-C5alkyl; or hydroxy-C1-C5alkyl. The compounds are useful as UV filters in sunscreen applications.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.Product Details of 92-36-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 92-36-4, in my other articles.

Reference：
Thiazole | C3H553NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS. In a Article，once mentioned of 16112-21-3, Application In Synthesis of 2-(4-Methylphenyl)benzothiazole

(-)-cis-2,3-Dihydro-3-(4-methylpiperazinylmethyl)-2-phenyl-1,5-benzothiazepin-4(5H)-one hydrochloride (BTM-1086) and its analogues, which possessed potent anti-ulcer and gastric secretory inhibiting activities, were synthesized and the structure of these compounds were established on the basis of spectral and chemical evidences.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.HPLC of Formula: C14H11NS, you can also check out more blogs about16112-21-3

Reference：
Thiazole | C3H916NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 5304-21-2. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 5304-21-2, Name is 6-Bromo-2-methylbenzo[d]thiazole

The excited radical anion of rhodamine 6G reduces heteroaryl bromides and chlorides to generate heteroaryl radicals that were successively trapped by pyrroles for the synthesis of heteroaromatic biaryls in moderate to excellent yields. The synthetically important photoredox catalytic C-H heteroarylation reaction works for a broad range of brominated electron-rich heteroarenes and chlorinated heteroarenes bearing electron withdrawing groups. In addition, this methodology was applied to the formal synthesis of a benzimidazole derivative II with interesting pharmacological properties.

If you are hungry for even more, make sure to check my other article about 5304-21-2. Reference of 5304-21-2

Reference：
Thiazole | C3H6807NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 131748-91-9, Name is 2-Bromo-5-(bromomethyl)thiazole,molecular formula is C4H3Br2NS, is a conventional compound. this article was the specific content is as follows.Formula: C4H3Br2NS

The present invention relates to compounds of formula I that are metallo-beta-lactamase inhibitors, the synthesis of such compounds, and the use of such compounds for use with beta-lactam antibiotics for overcoming resistance.

Do you like my blog? If you like, you can also browse other articles about this kind. Formula: C4H3Br2NS. Thanks for taking the time to read the blog about 131748-91-9

Reference：
Thiazole | C3H2476NS – PubChem,
Thiazole | chemical compound | Britannica

2516-40-7, Name is 2-Bromobenzothiazole, molecular formula is C7H4BrNS, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 2516-40-7, Recommanded Product: 2516-40-7

The present invention has offered a kind of ortho-carborane benzothiazole structure of semi-[…] complex and its preparation. The invention relates to a compound […] [Cp * IrCl2 ]2 As the raw material, it is connected to the n – BuLi, ortho-carborane benzothiazole reaction, to obtain ortho-carborane benzothiazole […] complex structure, the invention synthesis technique is simple green, has excellent selectivity and high yield. The invention iridium complex has stable physical and chemical properties and characteristics such as thermal stability, and under the condition of MAO as cocatalyst can be under the normal pressure effectively catalyze polymerization of ethylene, the obtained polymer also has relatively high molecular weight. (by machine translation)

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Formula: C7H4BrNS. In my other articles, you can also check out more blogs about 2516-40-7

Reference：
Thiazole | C3H2660NS – PubChem,
Thiazole | chemical compound | Britannica