Product Name: 2-Aminothiazole

Other Name: 2-Thiazolamine

CAS NO.: 96-50-4

Assay: 99.0%min

2-Aminothiazole, an important heterocyclic compound, has been widely used, and 2-aminothiazole compounds, too, are used in various fields because of their.

They are used in the treatment of allergies, hypertension, inflammation, schizophrenia, bacterial infections, HIV infections, osteoporosis, asthma, and gastrointestinal disorders.

In addition, many drugs such as penicillin, carboxypeptidase, transaminothiazole, anti-tumor drug Epothilone, estrogen receptor and adenosine antagonists, dopamine receptor agonists, angiotensin receptor antagonists, fibrinogen receptor antagonists (antithrombotic activity), bacterial DNA rotate inhibitors, Inhibitors of cyclin-dependent kinase (CDK), insecticides, fungicides, herbicides, schistosomicides, and anthelmintics also contain 2-aminothiazole rings.

There are also many antimicrobials, vitamins, flavors, and food additives that contain 2-aminothiazole structures.

2-Aminothiazoles are used as catalysts, corrosion inhibitors, dyes, and pharmaceuticals. They are also used in the synthesis of other organic compounds.

The most important industrial use of 2-Aminothiazoles is as corrosion inhibitors for steel in acidic environments. 2-Aminothiazoles are also used as catalysts in the manufacture of plastics, resins, and adhesives. Other uses include their role as dyes, pharmaceuticals, and intermediate compounds in the synthesis of other organic molecules.

2-Aminothiazole

What are the applications of 2-Aminothiazole?
There are many potential applications for 2-Aminothiazole, as it is a versatile and unique molecule. Some possible applications include:

-Acting as a corrosion inhibitor for metals

-Functioning as a herbicide

-Working as an intermediary in the production of dyes and pigments

- Acting as a photographic developer

- Use in the treatment of certain medical conditions, such as Alzheimer's disease, epilepsy, and depression

2-Aminothiazole has a wide range of applications due to its unique chemical structure. It can be used as an insecticide, herbicide, and fungicide, and has also been shown to be effective against certain cancers. 2-Aminothiazole is also being investigated for its potential use in treating Alzheimer's disease and other neurological disorders. With such a versatile chemical structure, it is likely that 2-Aminothiazole will continue to be studied for its potential uses in the future.

Clent Chemical, as a wholesaler of 2-Aminothiazole, sells products of good quality, looking forward to your visit and consultation.

【English name】2,2-Bipyridine

【Molecular formula】 C10H8N2

【Molecular Weight】 156.2

【CAS】366-18-7

【Abbreviations and aliases】α,α’-Dipyridyl,2,2-Bipyridine

【structural formula】



【Physical properties】White or light red crystalline powder, bp272~273 oC. Soluble in alcohol, ether, benzene, chloroform, and petroleum ether; soluble in water, its aqueous solution will appear red when it meets ferrous salt.

【Precautions】 This reagent is flammable and will produce toxic nitrogen oxide fumes when burned. Store 02 reactions in a fume hood.

2,2-Bipyridine is a very important organic ligand in organic chemistry, and because of its aromaticity, it can also undergo a series of reduction reactions, oxidation reactions, and C−H bond activation reactions.

2,2-Bipyridine reacts with osmium hexachloride overnight at high temperature to form the corresponding complex (Formula 1).

Organic Ligand Bipyridine

The reaction of 2,2-Bipyridine with silver perchlorate (I) at room temperature can generate the corresponding complex (Formula 2), and the reaction with cadmium diiodide (II) can obtain pyridine and iodine coordination in cadmium The above product (Equation 3)

Organic Ligand Bipyridine

2,2'-bipyridine can coordinate not only with metal but also with non-metal atom silicon. As shown in Formula 4:2,2-Bipyridine and dihydrosilane dichloride can form corresponding complexes in toluene solvent.

Organic Ligand Bipyridine

In addition to the outstanding coordination ability, because pyridine itself is an aromatic system, it also has the typical properties of aromatic compounds. Using hydrogen to reduce 2,2-Bipyridine in platinum dioxide hydrochloric acid acetic acid solution, the product with both pyridine rings completely reduced can be obtained (Formula 5). If m-CPBA is used to oxidize first, and then Pd/C is used to catalyze the hydrogenation reduction, the product with only one pyridine ring reduced can be obtained (Formula 6).

Organic Ligand Bipyridine

2,2-Bipyridine can be oxidized to 2,2-Bipyridine-1-nitroxide using m-CPBA (Equation7).

Organic Ligand Bipyridine

Under the catalysis of rhodium complexes, 2,2-Bipyridine and olefin compounds undergo double carbon-hydrogen activation reactions at the 3-position and 3’-position (Formula 8).

Organic Ligand Bipyridine

The reaction of 2,2-Bipyridine and diphenylzinc reagent under the catalysis of nickel complex can generate 6-phenyl-2,2-Bipyridine (Formula 9).