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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 124072-89-5 is helpful to your research. Related Products of 124072-89-5

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The present invention is directed to novel cytotoxic spliceostatin analogs (I) and derivatives, to antibody drug conjugates thereof, and to methods for using the same to treat medical conditions including cancer.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N2156 – PubChem

 

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The invention relates to hetaryl-substituted pyrazolidindione derivatives of formula (I), in which Het, A, D and G have the meanings cited in the description, to a number of methods for the production thereof, and to their use as pesticides and/or herbicides. The invention also relates to selective herbicidal agents that contain hetaryl-substituted pyrazolidindione derivatives and a compound that improves compatibility with cultivated plants.

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The present invention relates to new dithiinopyridazinedione derivatives, to processes for preparing them, to their use for controlling unwanted microorganisms, more particularly phytopathogenic fungi, in crop protection, in the household and hygiene sector and in the protection of materials, and also to crop protection compositions comprising these dithiinopyridazinedione derivatives.

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The present disclosure relates to a composition for dyeing keratin fibers, for example, human keratin fibers such as the hair, comprising at least one oxidation base chosen from diamino-N,N-dihydropyrazolone compounds and addition salts thereof, at least one coupler and at least one associative polyurethane polymer, and also to a dyeing process and kit using such a composition. The present disclosure makes it possible, for instance, to obtain fast coloration of keratin fibers that is resistant to light and to washing.

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One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Formula: C4H12Cl2N2, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 124072-89-5, Name is Hexahydropyridazine dihydrochloride, molecular formula is C4H12Cl2N2

The invention provides compounds of Formula I or Formula II: (I), (II) or a pharmaceutically acceptable salt or ester, thereof, as described herein. The compounds and compositions thereof are useful for treating Pneumovirinae virus infections. The compounds, compositions, and methods provided are particularly useful for the treatment of Human respiratory syncytial virus infections

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Pyridazine – Wikipedia,
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One of the oldest and most widely used commercial enzyme inhibitors is aspirin, name: Hexahydropyridazine dihydrochloride, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 124072-89-5

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The present invention provides benzoxazinones of formula I wherein R1 is hydrogen or halogen; R2 is hydrogen, C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-alkenyl, C3-C6-haloalkenyl, C3-C6-alkynyl, C3-C6-haloalkynyl, C1-C6-alkoxy or C3- C6-cycloalkyl-C1-C6-alkyl; R3 is halogen; R4 is halogen; X is O or S; and Y is a substituted or unsubstituted heterocycle; Benzoxazinones of formula I are useful as herbicides.

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Application of 124072-89-5, 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.124072-89-5, Name is Hexahydropyridazine dihydrochloride, molecular formula is C4H12Cl2N2. In a article,once mentioned of 124072-89-5

The preparation method comprises the following steps: firstly, reacting formic acid with hydrazine hydrate; then, reacting formic acid with hydrazine hydrate to generate N,N ? – tetrahydropyridazine-1, 2-N,N ? – diformaldehyde; finally, reacting tetrahydropyridazine-1, 1, 4 – 2-diformaldehyde with hydrochloric acid to form a hexahydropyridazine dihydrochloride. Compared with the prior art, compared with the prior art, the method has the advantages of easily available raw materials, low cost, mild reaction, simple operation, low requirement on reaction equipment and easy industrialization. (by machine translation)

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The invention is directed to novel cathepsin C inhibitors and their use in the treatment of diseases mediated by the cathepsin C enzyme. Specifically, the invention is directed to compounds according to Formula (I): wherein X and n are defined below, and to pharmaceutically-acceptable salts thereof. The compounds of the invention are cathepsin C inhibitors and can be used in the treatment of diseases mediated by the cathepsin C enzyme, such as COPD. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting cathepsin C and treatment of conditions associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

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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, 124072-89-5, name is Hexahydropyridazine dihydrochloride, introducing its new discovery. Recommanded Product: 124072-89-5

The present invention relates to naphthalene derivatives of formula (I) that are modulators of the glucocorticoid receptor, and to processes for the preparation and use of the same.

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Pyridazine – Wikipedia,
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Peptidomimetic inhibitors of bacterial peptide deformylase

A series of N-formyl hydroxylamine peptide deformylase inhibitors containing a cyclic azaamino acid moiety between the P1? and P3? substituents are presented. Selected compounds display antibacterial activity against pathogens associated with respiratory tract infections with representative compounds showing excellent MICs against Haemophilus influenzae.

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Pyridazine – Wikipedia,
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