Category: 890652-02-5

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called The oxidation of N-alkyl-3(5)-methyl-4-formylpyrazoles under phase-transfer catalysis, published in 2012, which mentions a compound: 890652-02-5, mainly applied to formylpyrazole derivative oxidation phase transfer catalysis, Application of 890652-02-5.

We have proposed a method of oxidation of pyrazole-4-carboxaldehydes to the corresponding carboxylic acids under phase-transfer catalysis at low temperature (20-30 °C) and with high yields (70-75%). Under these conditions, oxidation proceeds slowly but chemoselectively without oxidation of the Me group.

Although many compounds look similar to this compound(890652-02-5)Application of 890652-02-5, numerous studies have shown that this compound(SMILES:O=CC1=C(C)N(CCC)N=C1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

Computed Properties of C8H12N2O. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 5-Methyl-1-propyl-1H-pyrazole-4-carbaldehyde, is researched, Molecular C8H12N2O, CAS is 890652-02-5, about Identification of small-molecule inhibitors of Trypanosoma cruzi replication. Author is Germain, Andrew R.; Carmody, Leigh C.; Dockendorff, Chris; Galan-Rodriguez, Cristina; Rodriguez, Ana; Johnston, Stephen; Bittker, Joshua A.; MacPherson, Lawrence; Dandapani, Sivaraman; Palmer, Michelle; Schreiber, Stuart L.; Munoz, Benito.

We report the outcome of a high-throughput small-mol. screen to identify novel, nontoxic, inhibitors of Trypanosoma cruzi, as potential starting points for therapeutics to treat for both the acute and chronic stages of Chagas disease. Two compounds were identified that displayed nanomolar inhibition of T. cruzi and an absence of activity against host cells at the highest tested dose. These compounds have been registered with NIH Mol. Libraries Program (probes ML157 and ML158).

Compound(890652-02-5)Computed Properties of C8H12N2O received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5-Methyl-1-propyl-1H-pyrazole-4-carbaldehyde), if you are interested, you can check out my other related articles.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 5-Methyl-1-propyl-1H-pyrazole-4-carbaldehyde( cas:890652-02-5 ) is researched.Safety of 5-Methyl-1-propyl-1H-pyrazole-4-carbaldehyde.Attaryan, O. S.; Sahakyan, A. A.; Tamazyan, R. A.; Ayvazyan, A. G.; Asratyan, G. V. published the article 《Synthesis, structure, and properties of pyrazole-4-carbaldehyde oximes》 about this compound( cas:890652-02-5 ) in Russian Journal of General Chemistry. Keywords: pyrazolecarbaldehyde hydroxylamine stereoselective oximation; oxime pyrazolecarbaldehyde preparation mol crystal structure acetic anhydride dehydration; cyano pyrazole preparation. Let’s learn more about this compound (cas:890652-02-5).

1-Alkyl-1H-pyrazole-4-carbaldehyde oximes (preparation shown) reacted with acetic anhydride to give the corresponding nitriles, which is typical for anti isomers of aldoximes. The anti configuration of 5-methyl-1-propyl-1H-pyrazole-4-carbaldehyde oxime (I) in crystal was unambiguously determined by X-ray anal.

When you point to this article, it is believed that you are also very interested in this compound(890652-02-5)Safety of 5-Methyl-1-propyl-1H-pyrazole-4-carbaldehyde and due to space limitations, I can only present the most important information.

Reference:
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method