Tag: M.W:200-300

10344-42-0, Name is 4-Bromo-3,6-dichloropyridazine, belongs to pyridazine compound, is a common compound. Product Details of 10344-42-0In an article, once mentioned the new application about 10344-42-0.

Pesticidally active bi-or tricyclic heterocycles with sulphur-containing substituents, stereoisomers and tautomeric forms thereof that can be used as insecticides and can be prepared in a manner known per se.

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Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N3009 – PubChem

 

Reference of 679406-03-2, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 679406-03-2, Name is Ethyl 4,6-dichloropyridazine-3-carboxylate,introducing its new discovery.

The present invention relates to the use of novel compounds of formula I: wherein all variable substituents are defined as described herein, which are SYK inhibitors and are useful for the treatment of auto-immune and inflammatory diseases.

We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 679406-03-2, and how the biochemistry of the body works.Reference of 679406-03-2

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2961 – PubChem

 

Electric Literature of 679406-03-2, 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. 679406-03-2, Name is Ethyl 4,6-dichloropyridazine-3-carboxylate, molecular formula is C7H6Cl2N2O2. In a Patent£¬once mentioned of 679406-03-2

The present invention provides pyrazoles, isoxazoles, isothiazoles, thiadiazoles, and pyridazines according to Formula I as described herein, and pharmaceutically acceptable salts thereof. Pharmaceutical compositions and methods for treating primary hyperoxaluria, type I (PH) and kidney stones are also described.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Electric Literature of 679406-03-2. In my other articles, you can also check out more blogs about 679406-03-2

Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N2966 – PubChem

 

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, SDS of cas: 1178884-53-1, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 1178884-53-1, Name is 4-Bromo-6-chloro-2-methylpyridazin-3(2H)-one, molecular formula is C5H4BrClN2O

This application discloses compounds according to generic Formula I: wherein the variables are defined as described herein, and which inhibit Btk. The compounds disclosed herein are useful to modulate the activity of Btk and treat diseases associated with excessive Btk activity. The compounds are further useful to treat inflammatory and auto immune diseases associated with aberrant B-cell proliferation, such as rheumatoid arthritis. Also disclosed are compositions containing compounds of Formula I and at least one carrier, diluent or excipient.

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, SDS of cas: 1178884-53-1, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 1178884-53-1

Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N2994 – PubChem

 

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Application In Synthesis of 3-Iodo-6-methoxypyridazine. Introducing a new discovery about 17321-35-6, Name is 3-Iodo-6-methoxypyridazine

Provided are DC-89 derivatives represented by the formula: STR1 wherein X represents Cl or Br, R represents hydrogen or COR1, and W represents STR2 and pharmaceutically acceptable salts thereof. The compounds of the present invention have excellent anti-tumor activity and are useful as anti-tumor agents.

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.Application In Synthesis of 3-Iodo-6-methoxypyridazine, you can also check out more blogs about17321-35-6

Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N3023 – PubChem

 

Synthetic Route of 41933-33-9, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Patent, and a compound is mentioned, 41933-33-9, 2-Benzyl-4,5-dichloropyridazin-3(2H)-one, introducing its new discovery.

A novel 3(2H)-pyradazinone derivative of the formula (I) STR1 wherein, R represents an alkyl group having 1 to 4 carbon atoms substituted by a cycloalkyl group having 3 to 8 carbon atoms, an alkyl group having 1 to 4 carbon atoms substituted by a phenyl group which may be substituted or an alkyl group having 1 to 4 carbon atoms substituted by a heterocyclic group, R’ represents a hydrogen atom, a halogen atom, an alkoxy group having 1 to 4 carbon atoms or a hydroxyl group having 1 to 4 carbon atoms, J represents any of various organic radicals. There is also provided a process for preparing said derivatives. These derivatives are useful as active ingredients of insecticidal, acaricidal and/or nematicidal compositions for agricultural and horticultural uses as well as of expellent compositions for pests parasitic on animals.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 41933-33-9. In my other articles, you can also check out more blogs about 41933-33-9

Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N3196 – PubChem

 

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Formula: C4H2Br2N2O. Introducing a new discovery about 5788-58-9, Name is 4,5-Dibromopyridazin-3(2H)-one

HETEROARYLPIPERIDINE MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

The present invention is directed to compounds of the formula (I): (wherein R1, R2, R3, R4, R5, R6, R10 and n are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptor CCR-2.

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.Formula: C4H2Br2N2O, you can also check out more blogs about5788-58-9

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N3159 – PubChem

 

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Product Details of 5788-58-9. Introducing a new discovery about 5788-58-9, Name is 4,5-Dibromopyridazin-3(2H)-one

ANTIMICROBIAL AGENTS AND SCREENING METHODS

Disclosed herein are antibacterial and antimicrobial compositions and methods of use. Also disclosed are screening assays for identification of an agent that specifically inhibits DsbB or bVKOR. Such methods are useful, for example, in identifying antibacterial and antimicrobial agents and compositions.

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.Product Details of 5788-58-9, you can also check out more blogs about5788-58-9

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N3145 – PubChem

 

Reference of 91063-19-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.91063-19-3, Name is 3-(Benzyloxy)-6-chloropyridazine, molecular formula is C11H9ClN2O. In a Patent，once mentioned of 91063-19-3

Sulfonyl pyridazinone compounds useful as aldose reductase inhibitors

This invention relates to novel sulfonyl pyridazinone compounds useful as aldose reductase inhibitors in the treatment or prevention of certain complications arising from diabetes mellitus, pharmaceutical compositions comprising the sulfonyl pyridazinone, pharmaceutical compositions comprising a combination of the sulfonyl pyridazinone together with a second pharmaceutical agent, therapeutic methods comprising the administration of the sulfonyl pyridazinone compounds, therapeutic methods comprising the administration of the sulfonyl pyridazinone compounds in combination with a second pharmaceutical agent and compounds useful as intermediates for preparing the sulfonyl pyridazinone compounds of this invention.

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 91063-19-3

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2919 – PubChem

 

Application of 286946-24-5, 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.286946-24-5, Name is Methyl 3,6-dichloropyridazine-4-carboxylate, molecular formula is C6H4Cl2N2O2. In a article，once mentioned of 286946-24-5

NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS

Compounds of formula I, wherein R1, R2, R3, R4, Ra, X, X1, and Y are as defined herein or pharmaceutically acceptable salts thereof, inhibit HIV-1 reverse transcriptase and afford a method for prevention and treatment of HIV-1 infections and the treatment of AIDS and/or ARC. The present invention also relates to compositions containing compounds of formula I useful for the prevention and treatment of HIV-1 infections and the treatment of AIDS and/or ARC

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 286946-24-5

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2901 – PubChem