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What is the chemical structure of 2-bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride
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Looking at its name, "2-bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride", it is necessary to study its chemical structure in detail.
If you look at its name, "2-bromo", it shows that it has bromine atoms attached at the second position. "4,5,6,7-tetrahydro" means that at the 4th, 5th, 6th, and 7th positions, it is in the state of hydrogenation, that is, there are hydrogen atoms attached and it is saturated. "[ 1,3] thiazolo [5,4 - c] pyridine ", this is the core structure, [1,3] thiazolo [5,4 - c] pyridine is also called, that is, thiazolo ring and pyridine ring are conjugated in a specific formula. And" hydrochloride "means hydrochloric acid, which means hydrochloric acid forms a salt with it.
In summary, the structure of this compound is based on [1,3] thiazolo [5,4 - c] pyridine, with bromine atom substitution at position 2, and hydrogenation at positions 4, 5, 6, and 7, and the whole is in the form of hydrochloride. In this way, its chemical structure can be roughly understood.
What are the physical properties of 2-bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride
2-Bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride, this is an organic compound. Looking at its physical properties, under normal temperature and pressure, it is mostly in a solid state. Due to the interaction between atoms and the forces between molecules in the molecular structure, the molecules are arranged in an orderly manner and appear in a solid state.
When it comes to color, the pure state is usually white or off-white. Due to the absorption and reflection characteristics of the molecular structure of light, its absorption spectrum does not cover most of the region of visible light, so it appears this color.
Smell, the compound has a weak odor, because its molecular volatility is low, and the number of molecules that escape into the air at room temperature is rare, making it difficult to stimulate olfactory receptors, causing odor to be insignificant.
Its solubility is also an important physical property. In organic solvents, such as methanol, ethanol, dichloromethane, etc., there is a certain solubility. This is because these organic solvent molecules can form interactions such as hydrogen bonds and van der Waals forces with the compound molecules, which help them disperse in the solvent. However, the solubility in water is relatively low, because water is a highly polar solvent, and the overall polarity of the compound molecule is limited, and the interaction with water molecules is not enough to overcome the force between its own molecules, making it difficult to dissolve in water. The melting point of
has been experimentally determined to be within a certain temperature range (the specific value varies depending on the purity and measurement conditions). When the temperature rises to the melting point, the molecule obtains enough energy to overcome the lattice energy, the relative motion between the molecules intensifies, and the solid state changes to the liquid state. This melting point characteristic is of great significance for the identification, purification and processing application of the compound under specific conditions.
What is the main use of 2-bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride
2-Bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride has a wide range of uses. In the field of medicinal chemistry, this compound is often a key intermediate in the synthesis of many biologically active drug molecules. Due to its unique molecular structure, it can be combined with other chemical groups through various chemical reactions to build a complex molecular structure with specific pharmacological activities. It can be seen in the creation process of drugs for the treatment of various diseases, such as neurological diseases, cardiovascular diseases and other related drugs.
In the field of organic synthetic chemistry, it is also an important building block. Organic chemists can expand the complexity and diversity of molecules by performing various functional group conversion reactions on them, and use them to construct more complex and novel organic compounds to explore new materials, catalysts, etc., to promote the development and progress of the field of organic synthetic chemistry.
Furthermore, in the early stage of drug development activity screening, this compound may be used as a prototype of a lead compound for researchers to modify and optimize the structure. By changing its substituents, it can enhance its biological activity, improve its pharmacokinetic properties, and lay the foundation for the discovery and development of new drugs. Its importance in the fields of chemistry and medicine is evident from this, and it is an indispensable chemical substance.
What are the synthesis methods of 2-bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride
To prepare 2-bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride, there are many methods, and the common method is selected.
First, start with a compound containing a pyridine structure. First, under suitable reaction conditions, the pyridine ring meets with a sulfur-containing reagent with a specific substituent, and through nucleophilic substitution or cyclization, the basic structure of [1,3] thiazolo [5,4-c] pyridine is initially formed. Among these, the solvent, temperature and catalyst of the reaction are all key. If a polar organic solvent is selected, supplemented by a moderate temperature, the reaction can be promoted.
Then, the resulting intermediate is brominated. Usually, a brominating agent, such as bromine or a specific brominating agent, is used in an appropriate reaction system to precisely replace the hydrogen atom at the target position to obtain 2-bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine.
Finally, this product is reacted with hydrogen chloride gas or hydrochloric acid solution, and through salt-forming reaction, the final product is 2-bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride. When operating, pay attention to the pH value, temperature and time of the reaction to ensure the purity and yield of the product.
Second, you can also start from the construction of thiazole rings. The thiazole ring containing a specific substituent is first synthesized, and then the thiazole ring is connected to the pyridine ring through a clever reaction strategy to form the parent nucleus of the target compound. The desired product is also prepared through the process of bromination and salt formation.
These two types of methods have their own advantages and disadvantages. The former has common starting materials and relatively clear steps; the latter has an innovative strategy for constructing the parent nucleus, but the control of the reaction conditions is more stringent. In actual synthesis, the appropriate method needs to be carefully selected according to the availability of raw materials, cost, and difficulty of reaction.
2-Bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride What are the precautions during storage and use
2-Bromo-4,5,6,7-tetrahydro [1,3] thiazolo [5,4-c] pyridine hydrochloride, this is a special chemical substance. When storing and using, pay attention to many things.
First of all, let's talk about storage, because its nature may be active, it needs to be placed in a dry place. Humid air can easily cause it to deteriorate, just like wood in water rot. It should be stored in a cool place, avoiding heat like fire, under hot topics, lest its chemical changes and damage its quality. And it should be properly sealed to prevent excessive contact with air, causing oxidation or reaction of ingredients, just like a treasure box, to prevent it from contacting with undesirable things in the outside world.
As for the use, the operator must be familiar with its characteristics. Because many chemicals are potentially dangerous, toxic, or corrosive, full protection is required. Wear protective clothing, such as armor body protection; wear protective gloves, like iron hands to guard against danger; wear a protective mask, if the copper surface covers the danger, it can be safely operated. Furthermore, during use, the operation steps must be accurate and correct, according to the specifications, and cannot be changed at will. It is like marching into formation. If you make a mistake, you will lose everything. After use, the utensils also need to be properly cleaned to prevent subsequent problems caused by residual substances. In this way, you can ensure safe storage and use.