Iodomethyl 2s Cis 3 3 Dimethyl 7 Oxo 4 Thia 1 Azabicyclo 3 2 0 Heptane 2 Carboxylate 4 4 Dioxide
Iodobenzene
Iodomethyl (2s-cis)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylate 4,4-dioxide
FAQ

What is the chemical structure of iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo (3.2.0) heptane-2-carboxylate 4,4-dioxide?

My question is about the chemical structure of (2S-cis) -3,3-dimethyl-7-oxo-4-hetero-nitrogen-1-azabicyclo (3.2.0) heptyl-2-ene-4,4-dioxide. This is a rather technical chemical question, let me elaborate.

(2S-cis) indicates its stereochemical configuration, involving a specific arrangement of chiral centers. 3,3-dimethyl refers to the connection of two methyl groups at a specific location. The 7-oxo generation means that there is a place in the molecule where the oxygen atoms are connected in the form of carbonyl (C = O) to form a ketone structure. 4-hetero-nitrogen-1-azabicyclo (3.2.0) heptyl-2-ene describes the core skeleton of the molecule, which is a double ring structure, and the ring contains nitrogen atoms as heteroatoms, and there is a double bond at a specific position. 4,4-dioxide indicates that there are two oxygen atoms connected at a specific position, forming a special sulfur-oxygen double bond structure, etc. (specific needs to be judged in combination with the overall structure).

This structural characteristic endows the compound with unique chemical properties and reactivity, which may have important application and research value in many fields such as organic synthesis and medicinal chemistry. Its complex structure also brings many challenges and exploration space for chemical researchers. Advanced analytical methods and theoretical calculations are required to deeply understand its properties and functions.

What are the physical properties of iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo (3.2.0) heptane-2-carboxylate 4,4-dioxide?

What you are asking about is the physical properties of "3,3-dimethyl-7-oxo-4-hetero-nitrogen-1-azabicyclo (3.2.0) heptyl-2-ene-2-carboxylic acid amide 4,4-dicoxide". This compound is mostly in a solid state at room temperature. Its melting point is often in a specific temperature range due to the particularity of the molecular structure, but the exact value can be determined according to fine experiments.

In terms of solubility, due to the presence of both polar and non-polar groups in the molecule, it may have a certain solubility in polar solvents such as alcohols, while in non-polar solvents such as alkanes, the solubility may be low. Its density is also related to molecular accumulation and atomic weight, and is roughly within a certain range.

Furthermore, the stability of this compound is quite important. Due to the heteroatoms such as nitrogen and oxygen and the special double-ring structure, chemical stability needs to be carefully considered. Under specific conditions, reactions such as hydrolysis and oxidation may occur. Its volatility is relatively low, and due to the strong intermolecular forces, the molecules are not easy to escape into the gas phase.

As for other physical properties, such as refractive index, which are also closely related to the molecular structure, it needs to be accurately determined by professional instruments in order to be clear. In short, the physical properties of this compound are complex, which requires a combination of experimental investigation and theoretical analysis to gain in-depth insight.

What is the use of iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo (3.2.0) heptane-2-carboxylate 4,4-dioxide?

I think what you said is about "the use of 7-oxo-4-hetero-1-azabicyclo (3.2.0) heptyl-2-ene-2-carboxylic anhydride 4,4-dioxide". Although these substances are not directly stated in Tiangong Kaiwu, they may be useful based on ancient principles.

In ancient times, although there is no current precise chemical understanding, the investigation of the characteristics of various substances has not stopped. This 7-oxo-4-hetero-1-azabicyclo (3.2.0) heptyl-2-ene-2-carboxylic anhydride 4,4-dioxide, if it has specific chemical activity, may be helpful in pharmaceuticals. Ancient healers often used natural medicines to refine and treat diseases. If this compound can be extracted and purified by a specific method, it may add new power to the drug. It may adjust the medicinal properties to make the drug effect more accurate, or it can enhance the stability of the drug and help the drug survive for a long time without losing its effect.

Furthermore, in dyes and other processes, if this compound has a special color reaction or chemical properties, it may also bring new changes to the dyeing technique. In ancient dyeing workshops, the pursuit of bright and long-lasting dyes, if this substance can be closely combined with fabric fibers, or can show a unique color, it will certainly add a lot to the dyeing industry.

Although it is not detailed in "Tiangong Kaiwu", with the spirit of the ancients' exploration of materials, if this compound is encountered, it must be studied in detail, so that it can play a role in many fields such as pharmaceuticals and crafts, and add benefits to people's livelihood.

Iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo (3.2.0) heptane-2-carboxylate 4,4-dioxide What are the synthesis methods?

There are three methods for the synthesis of 4,4-dioxide.

One is to use kaidimethyl- (2S-cis) -3,3-dimethyl-7-oxo-4-hetero-nitrogen-1-azabicyclo (3.2.0) heptane-2-carboxylic acid ester as the starting material. After multiple steps of delicate transformation, during which or involving the increase, decrease, rearrangement and other changes of functional groups, the group at a specific position is first modified, and the molecule is gradually approached to the target structure by suitable reagents and conditions. In this way, it is necessary to precisely control the conditions of each step of the reaction, such as temperature, pH, catalyst dosage, etc. If there is a slight difference in the pool, it is easy to cause a cluster of side reactions, which affects the purity and yield of the product.

Second, you can find other compounds containing suitable functional groups as starting materials. After ingeniously designed reaction routes, or through condensation, oxidation, cyclization and other reaction sequences. First, the basic carbon frame is constructed by condensation reaction, and then the required oxygen atoms are introduced through oxidation steps. Finally, the cyclization forms the target double-ring structure, and the position and number of oxygen atoms are precisely regulated to obtain 4,4-dioxide. The key to this approach lies in the selection of starting materials and the planning of the reaction sequence. It is necessary to comprehensively consider the availability of raw materials, the difficulty of reaction and selectivity.

Third, it can also start from the existing similar structural compounds and undergo functional group transformation. Use the activity check point of the known compound, and modify it with specific reagents and reaction conditions. Or protect a functional group first, then modify other parts, and finally deprotect and complete the final transformation to achieve the synthesis of 4,4-dioxide. This approach focuses on the rational modification of the existing structure, and needs to be familiar with the mechanism and conditions of various functional group transformation to ensure the smooth progress of the reaction and obtain high-purity products.

Iodomethyl (2S-cis) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo (3.2.0) heptane-2-carboxylate 4,4-dioxide What are the precautions in storage and transportation?




First of all, it is related to the storage container. It must be filled with special and suitable utensils. The material must be resistant to the corrosion of dioxide, strong and not leaking, in order to ensure its safety. If the container is not good, it will cause the leakage of dioxide, which is very harmful.

Second, the place of storage should also be particular. It is advisable to choose a cool, dry and well-ventilated place, away from fire and heat sources, so as not to change its properties due to factors such as temperature and humidity, causing accidents. If placed in a high temperature place, the activity of dioxide or heat will increase greatly, and it is easy to change.

Furthermore, when transporting, the regulations must be strictly followed. The vehicle needs to be specially inspected to ensure its safety. The escort should also be familiar with the characteristics of dioxide and emergency methods. During transportation, beware of bumps and collisions. If the vehicle is damaged, the dioxide will escape, and the disaster will be imminent.

In addition, whether it is stored or transported, it needs to be clearly marked, clearly indicating that it is dioxide, so that everyone knows its danger, so that they can be treated with caution. And there should be a complete emergency plan. If something happens, they can respond quickly and reduce the damage.

In short, in the storage and transportation of dioxide, all details should not be ignored, and it must be handled with rigor and prudence to ensure safety.