Tag: M.W:200-300

In an article, published in an article, once mentioned the application of 16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole,molecular formula is C14H11NS, is a conventional compound. this article was the specific content is as follows.Computed Properties of C14H11NS

A variety of 2-arylbenzothiazoles were prepared by the direct reaction of 2-aminobenzenethiol and aryl aldehydes by the aid of activated carbon (Shirasagi KL or Darco KB) under oxygen atmosphere. 2-Pyridylbenzothiazole, thus obtained, was proved to work as an efficient ligand in palladium-catalyzed Mizoroki-Heck reaction.

Do you like my blog? If you like, you can also browse other articles about this kind. Computed Properties of C14H11NS. Thanks for taking the time to read the blog about 16112-21-3

Reference：
Thiazole | C3H798NS – 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. 101078-51-7, Name is 6-Methoxy-2-(p-tolyl)benzo[d]thiazole, molecular formula is C15H13NOS. In a Article，once mentioned of 101078-51-7, Safety of 6-Methoxy-2-(p-tolyl)benzo[d]thiazole

An efficient and practical method for the construction of 2-aryl-and 2-alkyl-substituted benzothiazoles via a copper-catalyzed redox condensation process between benzothiazoles and aldehydes or benzylic alcohols has been developed. The reaction proceeded under mild reaction conditions using environmentally benign tert-butyl hydroperoxide (TBHP) as the oxidant. A reaction mechanism involving the ring-opening of benzothiazoles initiated by the attack of acyl radical on the thiazole ring and intramolecular condensation is proposed based on the isolation of an anilide disulfide intermediate.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of 6-Methoxy-2-(p-tolyl)benzo[d]thiazole. In my other articles, you can also check out more blogs about 101078-51-7

Reference：
Thiazole | C3H7117NS – PubChem,
Thiazole | chemical compound | Britannica

Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn’t involve a screen. 5331-91-9, C7H4ClNS2. A document type is Article, introducing its new discovery., Recommanded Product: 5-Chlorobenzo[d]thiazole-2(3H)-thione

The direct acylation of sulfonamides by esters represents an attractive strategy in organic chemistry, being an interesting alternative to classical approaches to N-acylsulfonamides. Here is described a simple and effective method to obtain N-acylsulfonamides of pharmaceutical interest, in a reaction promoted by titanium(IV) chloride. This strategy was successfully applied to the synthesis of a peroxisome proliferator-activated receptor antagonist with a benzenesulfonimide moiety, ensuring an excellent yield of product. The reaction was further studied to explore the behavior of different -bromoesters and esters and the effects of para-substitution in the benzenesulfonamide moiety.

Interested yet? Keep reading other articles of 5331-91-9!, Recommanded Product: 5-Chlorobenzo[d]thiazole-2(3H)-thione

Reference：
Thiazole | C3H6290NS – PubChem,
Thiazole | chemical compound | Britannica

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 2875-32-3, Name is 2-(Benzo[d]thiazol-2-yloxy)acetic acid, Recommanded Product: 2875-32-3.

(20S) esters of camptothecin analogs are provided. The compounds are (20S) esters of an oxyalkanoic acid and camptothecin, which is optionally substituted at the 7, 9, 10, 11, and 12 positions of the camptothecin ring. The compounds are useful for treating cancer.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 2875-32-3. In my other articles, you can also check out more blogs about 2875-32-3

Reference：
Thiazole | C3H967NS – PubChem,
Thiazole | chemical compound | Britannica

17969-20-9, Name is 2-(2-(4-Chlorophenyl)thiazol-4-yl)acetic acid, molecular formula is C11H8ClNO2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 17969-20-9, COA of Formula: C11H8ClNO2S

Compounds of the formula: RC(O)O-spacer-OC(O)R?, wherein (i) RC(O)? is the acyl residue of an NSAID or other pharmaceutically active agent bearing a carboxylic acid function, (ii) spacer is Cn alkyl, (iii) n is from 1 to 6, and (iv) R? is substituted or unsubstituted heteroaryl or heterocycle, and pharmaceutical compositions thereof.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.COA of Formula: C11H8ClNO2S. In my other articles, you can also check out more blogs about 17969-20-9

Reference：
Thiazole | C3H392NS – PubChem,
Thiazole | chemical compound | Britannica

188672-83-5, Name is 6-Nitrobenzo[d]thiazole-2-carbonitrile, molecular formula is C8H3N3O2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 188672-83-5, Product Details of 188672-83-5

Methods and systems to generate 6-amino-6-deoxy-D-luciferin precursor, 2-cyano-6-aminobenzothiazole and related compounds and derivatives

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Product Details of 188672-83-5. In my other articles, you can also check out more blogs about 188672-83-5

Reference：
Thiazole | C3H7398NS – 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.50850-93-6, Name is Ethyl 2-aminobenzo[d]thiazole-6-carboxylate, molecular formula is C10H10N2O2S. In a Article，once mentioned of 50850-93-6, COA of Formula: C10H10N2O2S

Two series of analogues of riluzole, a blocker of excitatory amino acid mediated neurotransmission, have been synthesized: monosubstituted 2- benzothiazolamines and 3-substituted derivatives. Of all the compounds prepared in the first series, only 2-benzothiazolamines bearing alkyl, polyfluoroalkyl, or polyfluoroalkoxy substituents in the 6-position showed potent anticonvulsant activity against administration of glutamic acid in rats. The most active compounds displaying in vivo ‘antiglutamate’ activity were the 6-OCF3 (riluzole), 6-OCF2CF3, 6-CF3, and 6-CF2CF3 substituted derivatives with ED50 values between 2.5 and 3.2 mg/kg i.p. Among the second series of variously substituted benzothiazolines, compounds as active as riluzole or up to 3 times more potent were identified in two series: benzothiazolines bearing a beta-dialkylaminoethyl moiety and compounds with an alkylthioalkyl chain and their corresponding sulfoxides and sulfones. The most potent derivatives were 2-imino-3-(2-methylthio)- and 2-imino-3-(2- methylsulfinyl)-ethyl-6-trifluoromethoxybenzothiazolines (61 and 64, ED50 = 1.0 and 1.1 mg/kg i.p., respectively). In addition, intraperitoneal administration of some of the best benzothiazolines protected mice from mortality produced by hypobaric hypoxia.

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.COA of Formula: C10H10N2O2S, you can also check out more blogs about50850-93-6

Reference：
Thiazole | C3H10628NS – 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.51618-29-2, Name is 6-Chlorobenzo[d]thiazole-2-thiol, molecular formula is C7H4ClNS2. In a Patent，once mentioned of 51618-29-2, Computed Properties of C7H4ClNS2

The invention provides compounds of formula (I) having nematicidal, insecticidal, acaricidal and fungicidal properties, compositions comprising them and processes and intermediates for their preparation: STR1 wherein: X is oxygen or sulphur; n is 0, 1 or 2; R1, R2, R3, and R4 are as described in the specification.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 51618-29-2 is helpful to your research., Computed Properties of C7H4ClNS2

Reference：
Thiazole | C3H6990NS – 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, Safety of 2-(4-Methylphenyl)benzothiazole

A reusable thermal activated NHC precursor ionic liquid catalyst ([BMIm]2[WO4]) has been prepared and developed for the synthesis of nitrogen-containing heterocycles such as benzoxazinones and benzoazoles through imines activation. [BMIm]2[WO4] exhibited the good activity for the base-free condensation and oxidative NHC catalysis tandem under air atmosphere. The catalyst can be recovered and reused for at least five runs in gram scale synthesis without any decrease in catalytic activity. Furthermore, the control experiments demonstrated that the reaction involved formation of aromatic aldimines, NHC-catalyzed oxidative formation of imidoyl azoliums and intramolecular cyclization to generate the product.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 16112-21-3 is helpful to your research., Safety of 2-(4-Methylphenyl)benzothiazole

Reference：
Thiazole | C3H830NS – PubChem,
Thiazole | chemical compound | Britannica

Application of 383865-57-4. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 383865-57-4, Name is 4-Methoxy-7-morpholinobenzo[d]thiazol-2-amine

The present invention relates to a compound of the general formula (1). The compound of formula (1) is suitable for use in a method for treating a disorder relating to the binding of a galectin, such as galectin-3 to a ligand in a mammal, such as a human. Furthermore the present invention concerns a method for treatment of a disorder relating to the binding of a galectin, such as galectin-3 to a ligand in a mammal, such as a human.

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Reference：
Thiazole | C3H5291NS – PubChem,
Thiazole | chemical compound | Britannica