Iodomethyl (2s-cis) -3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylate What is the chemical structure of 4,4-dioxide

This is the chemical structure related to "iodomethyl (2S - cis) -3,3 - dimethyl - 7 - oxo - 4 - thio - 1 - azabicyclo [3.2.0] heptane - 2 - carboxylate 4,4 - dioxide". This compound has a complex structure and contains multiple specific groups.

From the nomenclature analysis, "iodomethyl" clearly shows that there is an iodine atom attached to the methyl group, which is an important structural substituent. " (2S - cis) " refers to a specific stereo configuration, the 2-carbon configuration is S-type, and the related groups are arranged cis. " 3,3-Dimethyl "indicates that there are two methyl groups attached to the 3-position carbon." 7-oxo "means that there is a carbonyl group at the 7-position." 4-thio-1-azabicyclo [3.2.0] heptane "constructs the core bicyclic skeleton, which is formed by a sulfur atom and a nitrogen atom, and the ring system has a specific number and connection method." 2-carboxylate "indicates that the 2-position is connected to the carboxylic acid ester group." 4,4-dioxide "refers to the connection of the 4-position sulfur atom to two oxygen atoms. The structure of

is composed of a unique dicyclic core with many different substituents. The interaction of each group determines the properties and reactivity of the compound.

Iodomethyl (2s-cis) -3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylate What are the main uses of 4,4-dioxide

Iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylate 4,4-dioxide, this is an organic compound with a wide range of uses.

In the field of medicine, as a key intermediate, it plays an important role in the synthesis of many drugs. Or can participate in the preparation of antibacterial drugs to help resist the damage of pathogens to the human body and protect the health of the people. Its unique chemical structure endows the synthesized drugs with specific pharmacological activities, enhancing the efficacy and pertinence of drugs.

In the field of organic synthetic chemistry, this compound is also an important cornerstone. With its special structure, chemists can build more complex and delicate organic molecular structures through various chemical reactions. This provides the possibility to explore new functional materials and develop high value-added chemicals, which greatly promotes the progress of organic synthetic chemistry.

At the level of scientific research and exploration, due to its special structure, it is often selected by researchers as a research object. Through in-depth study of its reaction characteristics and physicochemical properties, new chemical laws and reaction mechanisms may be revealed, contributing to the theoretical development of chemistry.

It can be seen that iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylate 4,4-dioxide has indispensable and important uses in many fields such as medicine, organic synthesis and scientific research, and is of great significance to promote the development of related fields.

What is the synthesis method of Iodomethyl (2s-cis) -3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylate 4,4-dioxide

To prepare iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylate 4,4-dioxide, the synthesis method is as follows:
First, take the appropriate starting material and construct the structure of the target molecule one by one through multi-step reactions. First, take the cyclic compound containing a specific substituent as the base, and use the common reactions in organic chemistry, such as nucleophilic substitution, oxidation, condensation, etc., to gradually introduce the required functional groups and modified structures.
In the nucleophilic substitution step, select the appropriate active halogenate, and react with the nucleophilic substrate in a suitable base and solvent system to achieve the purpose of precise introduction of groups. During the oxidation reaction, carefully select the appropriate oxidizing agent, control the reaction conditions, so that the specific sulfur atoms are oxidized to 4,4-dioxide state, and ensure that other parts of the molecule are not affected by excessive oxidation.
During the condensation reaction stage, adjust the ratio of reactants, temperature and reaction time to effectively connect each fragment into the target dicyclic structure. After each step of the reaction, separation and purification methods, such as column chromatography and recrystallization, are required to obtain high-purity intermediate products, thereby ensuring the quality and yield of the final product. The reaction conditions of each step need to be finely regulated. Temperature, pH, reaction time, etc. are all related to the success or failure of the reaction and the purity of the product. Repeated experiments and optimization are required to successfully prepare iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylate 4,4-dioxide.

What are the physical and chemical properties of Iodomethyl (2s-cis) -3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylate 4,4-dioxide

Iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylate 4,4-dioxide, this is an organic compound. Looking at its physical and chemical properties, the first thing to say about its properties is that it is a solid under normal conditions. Because many of these structural compounds have this state, their intermolecular forces make the molecules arranged in an orderly manner and appear as a solid state.

As for the melting point, due to the existence of various chemical bonds and functional groups in the molecule, the structure is complex, and the intermolecular forces are strong, so the melting point should not be low. In the molecule, polar functional groups coexist with non-polar parts, polar carboxylic acid ester groups and sulfur-oxygen double bonds, etc., interact with non-polar methyl groups, etc., so that the intermolecular forces are diverse, and the melting boiling point may be significantly affected by this.

In terms of solubility, in polar solvents, such as water, the molecule contains polar groups, or has a certain solubility, but the non-polar part will limit its solubility in water; in non-polar solvents, such as alkanes, due to the non-polar part, or has a certain solubility, then the polar group will reduce its solubility in non-polar solvents.

Chemically, the iodine methyl group it contains has high atomic activity and is prone to substitution reactions. When encountering a nucleophilic reagent, the iodine atom is easily replaced, and the nucleophilic reagent attacks the carbon atom of the iodine methyl group to form a new compound. Its double-ring structure imparts certain stability to the molecule. However, under specific conditions, such as strong acid-base or high temperature, the double-ring structure may undergo a ring-opening reaction, which changes the molecular skeleton. Carboxylic acid ester groups are also typically reactive and can undergo hydrolysis reactions. Under the catalysis of acids or bases, ester bonds are broken to form corresponding carboxylic acids and alcohols. The sulfur-oxygen double bond part can participate in the oxidation-reduction reaction, or be further oxidized, or a reduction reaction occurs under specific conditions, changing the oxidation state of the sulfur atom, which in turn affects the chemical properties of the entire

Iodomethyl (2s-cis) -3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylate prospects for 4,4-dioxide in the market

Iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylic acid 4,4-dioxide in the market?

Looking at this substance, it is a unique compound in the field of chemistry. However, in terms of market prospects, many factors really depend.

The first one is its use. If this compound can play important functions in key fields such as medicine and materials, the future may be very bright. For example, in the field of medicine, if it can be used as a novel drug intermediate to help create new drugs with excellent efficacy and minimal side effects, it will be favored by pharmaceutical companies, and the market demand may increase sharply.

Furthermore, the difficulty and cost of preparation are also key. If the preparation process is complicated, it requires huge amounts of capital and many resources, the cost remains high, and it is widely used, or the demand may be limited due to high price. On the contrary, if simple and economical preparation methods can be developed and their costs reduced, it is expected to expand the market.

The competitive situation should not be underestimated. If there are alternatives with similar efficacy and low cost in the market, this compound will face many challenges if it wants to stand out. It is necessary to demonstrate unique advantages, such as better performance and better environmental protection, in order to gain a place.

And the impact of policies and regulations cannot be ignored. In the pharmaceutical, chemical and other industries, policies and controls are strict. If this compound complies with relevant regulations and is approved to enter the market, it can enter the market freely; otherwise, it may be restricted and the prospect is bleak.

To sum up, iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylic acid 4,4-dioxide has both opportunities and challenges in the market. It is necessary to consider various factors such as use, cost, competition and regulations to obtain clarity.