N6 Propyl 4 5 6 7 Tetrahydro 1 3 Benzothiazole 2 6 Diamine Dihydrochloride Hydrate
Quinoline Thiophene Imidazole Thiazole
N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate
Chemical Name N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate
Molecular Formula C10H18Cl2N4S·xH2O
Appearance Solid (usually powder or crystalline)
Molar Mass Calculated based on x value in hydrate, e.g., anhydrous part: 309.25 g/mol (approx. without water)
Physical State Solid at room temperature
Solubility Soluble in polar solvents like water to some extent due to salt and polar groups
Melting Point Specific value depends on purity and hydrate state, needs experimental determination
Odor Typically odorless or very faint odor
Ph In aqueous solution, acidic due to dihydrochloride salt, pH < 7
Stability Stable under normal storage conditions, but may be sensitive to strong oxidizing agents
FAQ

What is the chemical structure of N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate

This is a substance whose chemical name is N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate. The chemical structure of the molecule is as follows:
The main structure of the molecule is 1,3-benzothiazole, which is a heterocyclic structure formed by fusing the benzene ring with the thiazole ring. The benzothiazole ring, at positions 4, 5, 6, and 7, are all saturated carbon atoms, forming the structural characteristics of tetrahydro, which means that the carbon-carbon double bonds at these positions have been hydrosaturated.
At positions 2 and 6, there are amino groups (-NH2O), respectively, showing the structural characteristics of diamines. The N6 position, that is, the nitrogen atom of the 6-position amino group, is connected with a propyl group (-CH -2 CH ⃣ CH 😉).
As for the form of dihydrochloride, it indicates that the organic amine compound reacts with hydrochloric acid, and the amino group binds two hydrogen ions to form a corresponding salt structure. Hydrate indicates that a certain proportion of water molecules are bound to the crystal structure of this compound.
In summary, the chemical structure of this substance has specific characteristics of heterocycles, substituents, salt formation and hydration.

What are the main uses of N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate

N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate is a chemical substance. It has a wide range of uses in the field of medicine and can be used as a key intermediate for the synthesis of new drugs. Drug developers hope to create new drugs with unique pharmacological activities and specific diseases by modifying and modifying their structures. For example, in the process of anti-inflammatory and anti-tumor drug development, the special chemical structure of this substance may be the key to combining with specific targets, helping to develop drugs with better efficacy and fewer side effects. < Br >
In the field of materials science, it may be an important raw material for the preparation of special functional materials. For example, by compounding with other organic or inorganic materials, it may be possible to give materials such as special optical, electrical or mechanical properties. For example, the preparation of materials with fluorescence properties can be applied to biological imaging, optical sensors and other fields; or to improve the conductivity of materials, providing new opportunities for the development of electronic devices.

Furthermore, in terms of scientific research and exploration, as a compound with a unique structure, it can provide novel research objects for organic synthesis chemistry. Scientists can use the study of its reaction properties to expand the methods and strategies of organic synthesis and promote the progress of organic chemistry. It can also deepen the understanding of basic chemical theories such as intermolecular forces by studying their interactions with other substances.

What is the safety of N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate

N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate is a complex chemical. Its safety is related to many aspects.

In terms of toxicity, it is difficult to determine without detailed research. However, in general, halide salts may have potential effects on organisms. In the form of dihydrochloride or under specific conditions, chloride ions and protons are released, which may change the cellular environment. If exposed to excess, it may cause cytotoxicity.

From the perspective of environmental impact, if this substance enters the environment, its degradability needs to be carefully investigated. If it is difficult to degrade or accumulates in the environment, it will affect the ecological balance. Its migration and transformation characteristics in environmental media such as water and soil are also unknown, or it may cause adverse effects on aquatic organisms, soil microorganisms, etc.

In terms of operational safety, due to its solid powder dihydrochloride hydrate in laboratory or industrial production operations, dust may be generated. If inhaled, it may cause irritation to the respiratory tract, or even cause more serious health problems. And if it comes into contact with the skin and eyes during operation, it may also cause irritation and damage. Therefore, the safety of N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate requires comprehensive and in-depth toxicological and environmental studies, and appropriate protective measures must be taken during operation to ensure human health and environmental safety.

What are the synthesis methods of N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate

To prepare N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate, there are many methods, and the following common methods are necessary.

Take 4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine as the base material and place it in an appropriate solvent, such as alcohol solvent, common ones are ethanol, methanol, etc. These solvents have good solubility to the reaction substrate and can stabilize the reaction environment. Subsequently, slowly add a propylation reagent, such as propyl halide, such as bromopropane. In this process, strict temperature control is required, usually maintained in a moderate temperature range, about 50-80 degrees Celsius is appropriate. If the temperature is too low, the reaction will be slow; if the temperature is too high, side reactions will easily occur. At the same time, in order to promote the reaction, an appropriate amount of alkali, such as potassium carbonate, sodium carbonate, etc., is often added, which can neutralize the acid generated by the reaction and shift the reaction equilibrium to the right.

After the propylation reaction is completed, N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine is obtained by separation and purification. Then, the product is dissolved in a suitable solvent, such as dichloromethane, chloroform, etc., into which hydrogen chloride gas is introduced, or concentrated hydrochloric acid is added to form amino groups into salts, generating N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride. In this step, the amount of hydrogen chloride needs to be precisely controlled, and excess or insufficient will affect the purity and yield of the product.

Finally, the generated N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride is hydrated. Generally speaking, it can be placed in a certain humidity environment, or slowly crystallized in solution, so that water molecules can be embedded in the lattice to form a hydrate. During this period, the crystallization conditions, such as temperature, solvent volatilization rate, etc., have a great impact on the crystal form and purity of the hydrate and need to be carefully regulated. In this way, through various steps, N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diaminodihydrochloride salt hydrate can be obtained.

What is the market prospect of N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate

N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate, in its appearance, this is a special chemical substance. In the current market, the demand for such fine chemicals is gradually becoming complex.

In the field of scientific research, with the rapid development of life sciences, drug development and other disciplines, the demand for such compounds is quite ardent. Many drug research and development institutions are dedicated to exploring new active pharmaceutical ingredients, N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate or because of its unique chemical structure, which can provide novel ideas for drug molecule design, so the demand is sometimes apparent in laboratory research.

In the industrial field, the synthesis of some special materials may also require this substance as a key intermediate. With the development of high-performance and multi-functional materials science, the quality and purity requirements of this compound are increasingly stringent.

However, at the market supply level, due to the difficulty of the synthesis process, the control requirements for reaction conditions are extremely high, resulting in limited production. And the raw materials required in the preparation process may not be easy to obtain and the price fluctuates greatly. Therefore, there are few manufacturers that can steadily supply high-quality compounds.

Although demand has increased, it is limited by the difficulty and cost of production. The circulation of N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate in the market has not yet reached sufficient territory. Although the market prospect is broad, it is still necessary to break through the bottleneck of production technology if it is to be developed.