Tag: M.W:100-200

Related Products of 141-30-0, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 141-30-0, Name is 3,6-Dichloropyridazine,introducing its new discovery.

CD73 INHIBITORS

The present invention provides 5-[5]-[2-cycloa Ikyl ]-6-pyridazin-3-yl ]- IH-pyrimidine-2,4-dione compounds, or pharmaceutically acceptable salts thereof, that inhibit the activity of CD73 and are useful in treating cancer. (Formula (I))

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Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N1275 – PubChem

 

Electric Literature of 1837-55-4, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1837-55-4, Name is 3,5-Dichloropyridazine, molecular formula is C4H2Cl2N2. In a Patent£¬once mentioned of 1837-55-4

COMBINATION PHARMACEUTICAL AGENTS AS RSV INHIBITORS

The present invention relates to pharmaceutical agents administered to a subject either in combination or in series for the treatment of a Respiratory Syncytial Virus (RSV) infection, wherein treatment comprises administering a compound effective to inhibit the function of the RSV and an additional compound or combinations of compounds having anti-RSV activity.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N1181 – PubChem

 

Synthetic Route of 141-30-0, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.141-30-0, Name is 3,6-Dichloropyridazine, molecular formula is C4H2Cl2N2. In a Article£¬once mentioned of 141-30-0

Selective deoxygenation of heteroaromatic N-oxides with olefins catalyzed by ruthenium porphyrin

A new convenient method of deoxygenation of heteroaromatic N-oxides is described. Ruthenium porphyrin was used as a catalyst and this method expressed high yields for o-substituted pyridine N-oxides, quinoline N-oxide derivatives, acridine N-oxide, etc. under mild conditions. Moreover, nitro-, benzyloxy-, and ketone carbonyl groups, which can be affected by the usual deoxygenation methods such as catalytic hydrogenation or borane reduction, were retained.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N1834 – PubChem

 

Chemistry is traditionally divided into organic and inorganic chemistry. name: 3-Phenyl-6-chloropyridazine, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent£¬Which mentioned a new discovery about 20375-65-9

Synthesis of steroidal triply-bridged cyclophanes

Steroidal triply-bridged cyclophanes are synthesised using cholic acid derivatives as bridge units; cyclophane 3 moderately binds to organic guest molecules and enantio-selectively binds to N-Z-phenylalanine.

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Pyridazine | C4H4N2678 – PubChem

 

Electric Literature of 88491-61-6, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 88491-61-6, Name is 3-Bromopyridazine,introducing its new discovery.

HERBICIDAL COMPOUNDS

Compounds of the formula (I) wherein the substituents are as defined in claim 1, useful as a pesticides, especially as herbicides.

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Pyridazine | C4H4N2135 – PubChem

 

Reference of 63910-43-0, 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 Article, and a compound is mentioned, 63910-43-0, 4-Chloro-5-methoxypyridazin-3(2H)-one, introducing its new discovery.

Retro-ene reaction, VI. Functionalization of 4,5-dihalopyridazin-6-ones using 1-acetyloxymethyl-4,5-dihalopyridazin-6-ones as the 1-o, 3-n, 5-o ene- adduct

Functionalization of 1-acetyloxymethyl-4,5-dihalopyridazin-6-ones via retro-ene reaction with some nucleophiles gave regioselectively only 5-halo- 4-substitutedpyridazin-6-ones.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Reference of 63910-43-0. In my other articles, you can also check out more blogs about 63910-43-0

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Pyridazine – Wikipedia,
Pyridazine | C4H4N2186 – PubChem

 

Reference of 35857-89-7, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 35857-89-7, Name is 6-Chloropyridazine-3-carbonitrile,introducing its new discovery.

TRICYCLIC INDOLE DERIVATIVES USEFUL ENDOTHELIAL LIPASE INHIBITORS

The present invention is directed to tricyclic indole derivatives, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions modulated by endothelial lipase, for example, cardiovascular disorders.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N845 – PubChem

 

Electric Literature of 20375-65-9, 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 Article, and a compound is mentioned, 20375-65-9, 3-Phenyl-6-chloropyridazine, introducing its new discovery.

Reagent-controlled diastereoselective synthesis of (2S,3R)- and (2R,3R)-2,3-diaminobutanoic acid derivatives using proline-catalyzed alpha-hydrazination reaction

(2S,3R)- and (2R,3R)-2,3-Diaminobutanoic acid (Dab) derivatives were efficiently synthesized from Cbz-(R)-alanine using the proline-catalyzed diastereoselective alpha-hydrazination reaction and the SmI2-promoted reductive cleavage of the N-N bond as the key steps.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Electric Literature of 20375-65-9. In my other articles, you can also check out more blogs about 20375-65-9

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Pyridazine – Wikipedia,
Pyridazine | C4H4N2692 – PubChem

 

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 1211587-01-7, name is 5-Chloropyridazine-3-carboxylic acid, introducing its new discovery. Product Details of 1211587-01-7

Angiotensin II receptor antagonists

Compounds are disclosed having the formula: STR1 The compounds of the invention are angiotensin II receptor antagonists.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N2037 – PubChem

 

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Quality Control of 3-Chloro-6-methylpyridazine, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 1121-79-5, name is 3-Chloro-6-methylpyridazine. In an article£¬Which mentioned a new discovery about 1121-79-5

3-(3-PYRIMIDIN-2-YLBENZYL)-1,2,4-TRIAZOLO[4,3-B]PYRIDAZINE DERIVATIVES AS MET KINASE INHIBITORS

Compounds of the formula (I), in which R1, R2, R3, R3?, R4 have the meanings indicated in Claim 1, are inhibitors of tyrosine kinases, in particular of Met kinase, and can be employed, inter alia, for the treatment of tumours.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N567 – PubChem