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Pyrazole CAS No.288-13-1

definition of a pyrazole

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Several pyrazole compounds have been reported to have anti-diabetic effects by acting as agonists on PPAR. According to the principle of ligand-receptor interaction reported in the docking study of pyrazole compounds with Ppargamma, this study was...
a novel pyrazole derivative

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Diabetes Mellitus (DM) is a metabolic disease caused by insulin secretion, insulin action or deficiency of both. Lack of insulin, in turn, can lead to chronic hyperglycemia and disrupt the metabolism of carbohydrates, fats, and proteins. Diabetes is...
pyrazole ring contains number of nitrogen

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Over the past two decades, a number of methods have been developed to address the limitations in the synthesis of substituted pyrazole Regioselectivity. Starting with simple building blocks, the one-pot approach to building complex examples has also...
1h-pyrazole-5-boronic acid pinacol ester

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Pyrazole and its related polycyclic analogues are common elements in a variety of bioactive compounds. These ring structures are essentially rare. As a result, they were previously thought to be low-molecular-weight components of potential new...
pyrazole contain oxygen as heteroatom

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Pyrazole compounds, a five-membered heterocycle containing two adjacent nitrogen atoms, are found to be the core structures of many molecules with a wide range of pharmaceutical and agricultural activities. In general, the classical method for...
why is pyrazole aromatic

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Pyrazole can also be used for lithium-hydrogen exchange, and then metal transfer to produce active substances, which can then participate in numerous cross-coupling reactions. Ethyl 3-methoxy-1-methyl-1h-pyrazole-4-carboxylate was effectively...
what different between pyrazole and imidazole

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PYRAZOLE can be selectively lithiated on different carbon atoms and then reacted with Electrophile depending on the mode of substitution. The deprotonation and subsequent carboxylation of 1-methyl-5-(trifluoromethyl) pyrazole are carried out mainly...
how to prepare pyrazole

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The reaction of 1,3-dione with hydrazine forms a five-membered heterocycle called pyrazole. The resulting enamines and imines make the heterocycles aromatic without the need for an oxidation step. The pyrazole ring system consists of five-membered...
knorr pyrazole synthesis procedure

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The synthesis of conopyrazole is an organic reaction for the conversion of hydrazine or its derivatives and 1,3-dicarbonyl compounds to pyrazole using acid catalysts. This mechanism begins with the acid-catalyzed formation of Imines, where in the...
is pyrazole an acid

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Over the past two decades, a number of methods have been developed to address the limitations in the synthesis of substituted pyrazole Regioselectivity. Substantive progress has also been made in building complex examples in one stop, starting with...
molecular weight for pyrazole

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PYRAZOLES are aromatic 5-diazoles with a variety of chemical and biological characteristics, but they also have a rich and interesting history. The reaction of 1,3-dicarbonyl compounds quickly proved to be useful for the synthesis of other...
pyrazole on reaction with hno3 is to form

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At the 1883, the German chemist Ludwig Quenord gave the term pyrazole to such compounds. In the classic method developed by the German chemist Hans Pechmann in 1898, pyrazole was synthesized from acetylene and diazomethane. Pyrazole is an organic...
pyrazole and imidazole ligands

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The remarkable chemical diversity of Heterocyclic compound is still associated with drug discovery. In the past few decades, drug development has been a major component of the rapid maturation of the field of Medicinal Chemistry. In the meantime,...
knorr pyrazole synthesis pdf

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Free radicals are highly reactive chemicals that can damage cells and attack healthy cells, potentially damaging molecules. Free radicals can be harmful to the body and destroy all the major components of cells, including DNA, proteins and cell...
why pyrrole is less basic than imidazole

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Antimicrobial agents are compounds used to kill or inhibit the growth of microorganisms. They can be grouped according to the microorganisms in which they act. In fact, many diseases are caused by these microorganisms, which pose a great threat to...
how is pyrazole made

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Cancer is a group of diseases characterized by abnormal cell growth that can invade or spread to other parts of the body. There are more than 100 types of cancer, including breast, skin, lung, colon, prostate and lymphoma. Symptoms vary according to...
pyrazole and imidazole basicity

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Insecticides are substances used to kill insects. ACARICIDES are specifically used to kill members of the subclass of spiders, including the tick and Mites. Both pesticides and acaricides are used in agriculture and medicine, although their primary...
is pyrazole soluble in water

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Herbicides (commonly known as herbicides) are pesticides used to remove harmful plants. These unwanted plants, called weeds, compete with productive crops or pastures and eventually turn productive land into unusable shrubbery. Weeds can be toxic or...
is pyrazole a chemical compound

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DNA gyrase is an essential bacterial enzyme involved in DNA replication, transcription and recombination. It belongs to a class of enzymes called topoisomerase that are involved in the topological transformation of DNA. The ATP-dependent negative...
pyrazole and imidazole difference

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Pyrazole ring is a prominent structural motif found in many drug-active compounds. This is mainly due to its ease of preparation and pharmacological activity. The selective functionalization of pyrazoles with various substituents has also been found...
pyrazole derivatives as anticancer agents

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Heterocycles with pyrazole rings are also of interest because of their use as synthetic reagents in Multi-component reaction, chiral auxiliaries, and Guanosine acidifiers. Various substituted pyrazoles have also been found to be used as chelating...
melting point for pyrazole

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Pyrazole derivatives represent one of the most active classes of compounds and have a wide range of biological activities. Several drugs have been developed from pyrazole derivatives in recent years. CELECOXIB, for example, showed anti inflammatory...
pyrazole synthesis and reactions

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Heterocycles are widely distributed in nature and play a crucial role in metabolism because their structural subunits are found in many natural products, including vitamins, hormones, antibiotics and alkaloids, as well as drugs, pesticides, dyes and...
reductive amination with pyrazole

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Heterocycles are a class of very important and unique compounds. They account for more than half of all known organic compounds and have a wide range of physical, chemical and biological properties, covering a wide range of reactivity and stability....

China Pyrazole CAS No.288-13-1 Suppliers

Pyrazole, also known as 1,2-diazoles, Diazene Pentacyclines, o-diazepines; is White needle-shaped or prismatic crystal, from ethanol crystallization of pyrazole is colorless needle-shaped crystal. Pyridine-like odor and pungent bitter taste, soluble in water, alcohol, ether and benzene. The boiling point and melting point of the compounds increased when there were substituents on the carbon atoms, and decreased when there were substituents on the nitrogen atoms. Chlorination, bromination, iodination, alkylation and acylation are easy to occur. The formula is C3H4N2.

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Indicators

Electronic grade

Pharmaceutical grade

Pesticide Grade

Appearance

Natural Grain Crystal

Crystallization of natural particles or mechanical granulation

Mechanical

Granulation

Content (%) ,

chromatographic method ≥

99.5

99

98.5

Whiteness(r457)

Natural Crystal: Colorless Transparent Crystal

Mechanical Granulation

≥60

Natural Crystal: Colorless Transparent Crystal

Mechanical

Granulation

≥55~<60

Moisture content (%) ≤

0.5

0.8

1.0

Fe+ (%) ≤

0.00005

--

--

Melting point

67.0~70.0

67.0~70.0

67.0~70.0


Packaging, transportation and storage:

Pyrazole is transported in sealed plastic-lined cardboard or iron drums and stored in dry, ventilated, rain-proof and sun-proof places to avoid mixing with hydroxide. Keep away from heat and open flames.

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