Tag: M.W:100-200

Synthetic Route of 61090-37-7, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.61090-37-7, Name is 2,3-Dihydrobenzofuran-4-amine, molecular formula is C8H9NO. In a Patent，once mentioned of 61090-37-7

A chemical compound of formula (I) wherein R1 and R2 are independently selected from hydrogen and alkyl; R3 is alkyl; R4 and R5 are selected from hydrogen and alkyl; R6 and R7 are independently selected from hydrogen, halogen, hydroxyl, alkyl, aryl, amino, alkylamino, dialkylamino, alkoxy, aryloxy, alkylthio, alkylsulfoxyl, nitro, carbonitrile, carbo-alkoxy, carbo-aryloxy and carboxyl; and A is a 5-or 6-membered ring optionally containing one or more heteroatoms wherein the atoms of the ring A, other than the unsaturated carbon atoms of the phenyl ring to which the ring A is fused, are saturated or unsaturated, and pharmaceutically acceptable salts, addition compounds and prodrugs thereof; and the use thereof in therapy, particularly as an agonist or antagonist of a 5HT receptor, particularly a 5HT2C receptor, for instance in the treatment of disorders of the central nervous system; damage to the central nervous system; cardiovascular disorders; gastrointestinal disorders; diabetes insipidus, and sleep apnea, and particularly for the treatment of obesity.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 61090-37-7

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H474O – PubChem

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Quality Control of 4,5-Difluorophthalic Anhydride, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 18959-30-3, Name is 4,5-Difluorophthalic Anhydride, molecular formula is C8H2F2O3

A novel carborane-containing phenylethynyl terminated imide compound (Carb-PEPA) as a modifier for fluorinated phenylethynyl terminated imide oligomer (AFR-PEPA) was synthesized and characterized by FT-IR and 1H-NMR. The resin systems consisting of Carb-PEPA and AFR-PEPA (AFR-PEPA-Carb) were prepared with different weight fractions of Carb-PEPA. The thermal curing kinetics and thermal stability of the imide compound and resultant resin systems were analyzed by using DSC and TGA respectively. The relevant kinetic data were determined by a Kissinger method. The results show that the glass transition temperatures (Tg) of the cured resin systems increase with the addition of Carb-PEPA. The imide system containing 20 wt% Carb-PEPA (AFR-PEPA-Carb-20) exhibits the highest Tg of 389.5 C due to the high steric hindrance of carborane. The char yield of the resin was also increased with the introduction of the carborane structure in the system. The kinetic data indicate that AFR-PEPA/Carb-PEPA imide blends have higher activation energy E and frequency factor A than AFR-PEPA imide oligomers.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Quality Control of 4,5-Difluorophthalic Anhydride, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 18959-30-3, in my other articles.

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2984O – PubChem

14963-96-3, Name is 4-Methoxyisobenzofuran-1,3-dione, belongs to benzofurans compound, is a common compound. name: 4-Methoxyisobenzofuran-1,3-dioneIn an article, once mentioned the new application about 14963-96-3.

A simple and convenient synthesis of 3-methoxyphthalic anhydride by a two-step synthesis involving Diels-Alder reaction of 2-methoxyfuran with maleic anhydride is reported.

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 14963-96-3

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2879O – PubChem

Application of 3199-61-9, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 3199-61-9, molcular formula is C11H10O3, introducing its new discovery.

An expedient synthesis of enantioenriched substituted (benzofuran-yl)-aryl and heteroaryl carbinols, is described. A key feature of this protocol is synthesis of functionally varied benzofuran scaffolds via a Rap-Stoermer reaction/catalytic asymmetric transfer hydrogenation (ATH) using substituted salicylaldehyde and alpha-haloaryl, heteroaryl ketones.

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 3199-61-9 is helpful to your research. Application of 3199-61-9

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H3036O – PubChem

Synthetic Route of 496-41-3, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 496-41-3, Name is Benzofuran-2-carboxylic acid,introducing its new discovery.

A series of heterobiaryl amides was designed and synthesized as novel mGluR5 antagonists. The synthesis using palladium catalyzed Suzuki-Miyaura cross-coupling reactions provided an array of compounds with a range of in vitro activities. In particular, compound 9e, 4(3,5-difluorophenyl)-N-(6-methylpyridin-1-yl)picolinamide, exhibited nanomolar affinity at the mGluR5 and will serve as a template for future drug design.

We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 496-41-3, and how the biochemistry of the body works.Synthetic Route of 496-41-3

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H1854O – PubChem

Related Products of 82104-74-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.82104-74-3, Name is 1-Oxo-1,3-dihydroisobenzofuran-5-carbonitrile, molecular formula is C9H5NO2. In a Patent，once mentioned of 82104-74-3

The present invention relates to fused cyclic urea derivatives which have antagonistic activities against CRHR1 and/or CRHR2, and which are useful in the treatment or prevention of disorders and diseases in which CRHR1 and/or CRHR2 is involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which CRHR1 and/or CRHR2 is involved.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 82104-74-3

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H1542O – PubChem

Application of 4790-81-2, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.4790-81-2, Name is Benzofuran-7-ol, molecular formula is C8H6O2. In a article，once mentioned of 4790-81-2

Compounds of the structure; STR1 and pharmaceutically acceptable salts thereof, wherein: R1 is H, alkyl, alkoxy, carboxyl, alkylcarboxy, trifluoromethyl, halogen, nitro or hydroxy; X is O, N, S or C; Y is O, N or S; and R2 is H, alkyl, cycloalkyl, aryl or heteroaryl useful in the treatment of ischemic heart disease and hypertriglyceridemia.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 4790-81-2

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H438O – PubChem

Electric Literature of 652-39-1, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.652-39-1, Name is 4-Fluoroisobenzofuran-1,3-dione, molecular formula is C8H3FO3. In a article，once mentioned of 652-39-1

The present invention provides compounds, compositions thereof, and methods of using the same.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 652-39-1

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2486O – PubChem

4265-25-2, Name is 2-Methylbenzofuran, belongs to benzofurans compound, is a common compound. Formula: C9H8OIn an article, once mentioned the new application about 4265-25-2.

The establishment of permanent fish cell cultures dates back in the early 1960s and since then more than 283 fish cell lines have been developed. The cells were isolated from a broad range of tissues such as ovary, fin, swim bladder, heart, spleen, liver, eye muscle, vertebrae, brain, skin and especially embryos from different fish species. In contrast to mammals, fish cell lines are derived from normal tissues, with only a few exceptions isolated from epithelioma or hepatoma Cultured fish cells were used for genotoxicity assessment for the first time in 1979,2 when transformed cells derived from a primary culture of embryonic tissue of butterfly splitfin (Ameca splendens) were used for the evaluation of the induction of sister chromatid exchanges (SCEs) by carcinogens/mutagens. Since then, a variety of different fish cell lines have been successfully introduced for the detection of a large variety of genotoxic endpoints. As most fish karyotypes consist of large numbers of small, irregular chromosomes, chromosomal aberrations (CA), which are usually detected in metaphase-blocked cells, are difficult to discern and to interpret in fish cells, thus the analysis is complicated and time-consuming. Therefore, other methods such as micronucleus assay are recommended for the assessment of chromosomal damage instead of SCE and CA in fish cells (Figure 13.1).

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 4265-25-2

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H22O – PubChem

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, category: benzofuran, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 54802-10-7, Name is 3-Aminobenzofuran-2-carboxamide, molecular formula is C9H8N2O2

An object of the present invention is to provide a novel AMPA receptor potentiator. A compound represented by the following formula (I) or a salt thereof: wherein in formula (I) R1 represents (1) a halogen atom, or (2) cyano group, or the like; Ra and Rb each independently represent a hydrogen atom or C1-4 alkyl; L represents a bond, or a spacer in which the number of atoms in the main chain is 1 to 8; Ring A represents (1) a non-aromatic carbon ring of 4-8 carbon atoms, or (2) a 4- to 8-membered non-aromatic heterocycle either of which is optionally substituted with 1 or more substituents selected from (a) halogen atoms, and (b) cyano group; and Ar represents a substituted phenyl group, or optionally substituted 5- or 6-membered aromatic heterocyclic group.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. category: benzofuran, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 54802-10-7, in my other articles.

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2810O – PubChem