6 Methoxy 2 Benzothiazolecarbonitrile
Quinoline Thiophene Imidazole Thiazole
6-methoxy-2-Benzothiazolecarbonitrile
Chemical Formula C9H6N2OS
Molecular Weight 190.22 g/mol
Appearance Solid (usually powder)
Physical State At Room Temp Solid
Melting Point 128 - 132 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in some organic solvents like DMSO, chloroform
Odor Odorless (usually)
Color Off - white to light yellow
FAQ

What is the chemistry of 6-methoxy-2-Benzothiazolecarbonitrile?

6-Methoxy-2-benzothiazolecarbonitrile is an organic compound. Its physical and chemical properties are unique and it is widely used in many fields.

First of all, its physical properties, under room temperature and pressure, 6-methoxy-2-benzothiazolecarbonitrile is often in a solid state. Its melting point, boiling point and other data are of great significance to define its physical state under different temperature conditions. Sadly, it is difficult to describe in detail because there is no exact data. However, according to the general law of organic compounds, the structure of nitrile groups and methoxy groups may cause its melting point to be relatively high, due to the strong intermolecular force.

As for the chemical properties, the nitrile group in 6-methoxy-2-benzothiazole formonitrile has high reactivity. The nitrile group can be hydrolyzed to form carboxyl groups, and this reaction can occur under acidic or basic conditions. For example, in an alkaline environment, the nitrile group is first hydrolyzed to amide, and then hydrolyzed to carboxylic acid. This reaction is often a key step in organic synthesis and can be used to prepare derivatives containing carboxyl groups.

Furthermore, the presence of methoxy groups also affects the chemical properties of the compound. Methoxy groups are the power supply groups, which can increase the electron cloud density on the benzothiazole ring, thereby affecting its electrophilic substitution reactivity. Compared with the methoxy-free analogues, 6-methoxy-2-benzothiazole formonitrile is more likely to react in the ortho and para-positions of the methoxy group in the electrophilic substitution reaction.

In addition, the benzothiazole ring itself has certain aromaticity, which endows the compound with certain stability. However, because of the functional groups such as methoxy and nitrile groups connected to the ring, it has unique reactivity and can participate in a variety of organic reactions, such as addition reactions with nucleophiles, showing potential application value in drug synthesis, materials science and other fields.

What are the physical properties of 6-methoxy-2-Benzothiazolecarbonitrile?

6-Methoxy-2-benzothiazolecarbonitrile is one of the organic compounds. Its physical properties are quite important and it is widely used in the fields of chemical industry and materials science.

The properties of this compound are mostly white to light yellow crystalline powder under normal conditions. Looking at its color, the pure color is white and moist, and if it contains impurities, it may be light yellow. The powder has a fine texture and is slippery when twisted by hand.

Melting point is the key physical quantity characterizing the properties of this compound. After experimental determination, the melting point of 6-methoxy-2-benzothiazolecarbonitrile is in a specific temperature range. The accurate determination of this temperature range is crucial for the quality control of its synthesis and application. Determination of melting point is also an important means to identify the purity of this compound. The melting point of pure products is relatively fixed. If it contains impurities, the melting point may decrease and the melting range may widen.

In terms of solubility, 6-methoxy-2-benzothiazolecarbonitrile has different behaviors in organic solvents. In common organic solvents such as ethanol and acetone, it has a certain solubility. In ethanol, it can be seen that it gradually dissolves and forms a uniform solution when heated and stirred moderately. However, in water, its solubility is very small and almost insoluble. The difference in solubility is due to the characteristics of its molecular structure. The molecule contains hydrophobic groups, so it is difficult to dissolve in water with strong polarity, and has good affinity in organic solvents with moderate polarity.

In addition, the density of 6-methoxy-2-benzothiazolecarbonitrile is also one of its physical properties. Although its density data needs to be accurately measured experimentally, its density has an impact on its mixing and separation with other substances in practical applications. Understanding its density is helpful for rationally designing the process flow in industrial production to ensure the quality and yield of the product. The determination of its density is often carried out according to the Archimedes principle and other related methods, and the operation process needs to be fine in order to obtain accurate data.

What are the common synthetic methods of 6-methoxy-2-Benzothiazolecarbonitrile?

A common method for the synthesis of 6-methoxy-2-benzothiazole carbamonitrile often uses benzothiazole as the starting material. The method is as follows:
First take benzothiazole containing an appropriate substituent, mix it with a base in a suitable solvent. Alkalis, such as sodium hydride, potassium carbonate, etc., can activate benzothiazole molecules to make them more reactive.
Second, add halogenated formonitrile compounds, such as chloroacetonitrile, bromoacetonitrile, etc. Here, the halogen atom is very active and can undergo nucleophilic substitution reaction with benzothiazole activated by base. Under heating or specific catalytic conditions, the halogen atom leaves, and the specific position of benzothiazole is connected to the methonitrile group, gradually forming the target product 6-methoxy-2-benzothiazole formonitrile.
There are also other compounds as starting materials and obtained by multi-step reaction. The benzothiazole ring is first constructed with appropriate raw materials, and then methoxy and methonitrile are introduced. This multi-step reaction requires fine control of the reaction conditions of each step, such as temperature, reactant ratio, reaction time, etc., to obtain a product with higher yield and purity.
Another synthesis path is catalyzed by transition metals. The selection of transition metal catalysts such as palladium and copper can promote the selective reaction. In the catalytic system, ligands are added to regulate metal activity and selectivity. Transition metal catalysis can make the originally difficult reaction proceed smoothly and improve the synthesis efficiency of 6-methoxy-2-benzothiazolecarbonitrile.
When synthesizing, it is necessary to pay attention to the influence of reaction conditions on the product. Too high or too low temperature can cause side reactions or abnormal reaction rates; improper proportion of reactants also affects the yield. And the post-treatment process is also critical. The product often needs to be purified by extraction, column chromatography, etc., to obtain high-purity 6-methoxy-2-benzothiazolecarbonitrile.

6-methoxy-2-Benzothiazolecarbonitrile in what areas?

6-Methoxy-2-benzothiazolecarbonitrile has a wide range of uses. In the field of medicine, it is a key intermediate for the synthesis of many specific drugs. For example, some targeted therapeutic drugs for specific diseases, 6-methoxy-2-benzothiazolecarbonitrile can be ingeniously chemically converted into the molecular structure of the drug, giving the drug the ability to accurately act on diseased cells, improving the therapeutic effect, and reducing the damage to normal cells at the same time, providing a strong boost for the treatment of difficult diseases.

In the field of materials science, it also has good performance. It can participate in the preparation of functional materials, and after special processing, the resulting materials are unique in terms of optical and electrical properties. For example, for the manufacture of new photoelectric conversion materials, in solar cells and other devices, it can effectively improve the photoelectric conversion efficiency and promote technological innovation in the energy field.

Furthermore, in the research and development of pesticides, 6-methoxy-2-benzothiazolecarbonitrile can be used as an important starting material. The pesticides derived therefrom have high killing or inhibitory activity against specific pests or bacteria, and are less toxic and better environmentally compatible than traditional pesticides, safeguarding the sustainable development of agriculture.

In addition, in the field of organic synthetic chemistry, it is a compound with a unique structure that provides the basis for the construction of many complex organic molecules. With their special functional groups, chemists can synthesize organic compounds with novel structures and unique properties through exquisite reaction design, continuously expanding the boundaries of organic chemistry and laying the foundation for the development of new materials and drugs in various fields.

What is the market outlook for 6-methoxy-2-Benzothiazolecarbonitrile?

6-Methoxy-2-benzothiazolecarbonitrile is a key chemical intermediate in the field of organic synthesis. In the field of pharmaceutical research and development, it can be used as a building block for the construction of specific bioactive compounds, or as a starting material for the creation of new drugs. In the long journey of innovative drug research and development, it may be able to give new properties to drug molecules by virtue of its unique chemical structure, thereby helping to deal with various diseases. In the field of materials science, it may be possible to participate in the synthesis of materials with special properties, such as materials with unique optical and electrical properties, to meet the development needs of electronic devices, optical instruments and other industries.

However, looking at the current market situation, although the application prospect is broad, its market scale may still be limited. Due to the complexity of the synthesis process, the production cost remains high, restricting its large-scale production and wide application. And the depth and breadth of related research may yet to be expanded, and many potential application scenarios have not been fully explored. Furthermore, the market competition landscape is not fully clear. Although some enterprises and scientific research institutions are involved in this field, a solid industrial ecology has not yet been formed.

However, looking to the future, with the continuous progress of science and technology, the synthesis technology is expected to break through innovation, and the production cost may be greatly reduced, thereby promoting the gradual expansion of the market scale. With the rapid development of the field of medicine and materials science, the demand for 6-methoxy-2-benzothiazolecarbonitrile may also increase day by day. Over time, through the unremitting research of scientific researchers and the active promotion of the industry, its market prospects may gradually become clear, and it will bloom in more fields and become an important force to promote the development of related industries.