Competitive (S)-2-(2-Iodophenyl)Pyrrolidine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to
sales7@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
As a leading (S)-2-(2-Iodophenyl)Pyrrolidine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What is the chemical structure of (s) -2- (2-iodophenyl) pyrrolidine?
(S) - 2 - (2 - iodophenyl) pyrrolidine is also an organic compound. The analysis of its chemical structure is related to the category of organic chemistry.
Among this compound, pyrrolidine is its core structure. Pyrrolidine is a compound containing a five-membered nitrogen heterocycle with unique chemical properties. In this (s) - 2 - (2 - iodophenyl) pyrrolidine, the second carbon of the pyrrolidine ring is connected to a specific substituent.
The substituent connected is (2 - iodophenyl). The phenyl group is the structural unit of the benzene ring, which has aromatic properties and gives the compound a specific electron cloud distribution and stability. The ortho (2-position) of the benzene ring is complex with iodine atoms. The iodine atom has a relatively large atomic mass and strong electronegativity, and its existence significantly affects the electron cloud density and spatial structure of the molecule.
As for the one shown in (s), it refers to the three-dimensional configuration of the compound. In organic chemistry, three-dimensional chemistry is very important. The (s) configuration indicates that the spatial arrangement of the molecules of this compound follows specific rules, which affects its physical and chemical properties and plays a key role in chemical reactions and biological activities.
In summary, the chemical structure of (s) -2- (2-iodophenyl) pyrrolidine is composed of a pyrrolidine ring, a (2-iodophenyl) substituent and a specific (s) stereo configuration. The interaction of various elements determines the unique chemical behavior and properties of the compound.
What are the main uses of (s) -2- (2-iodophenyl) pyrrolidine?
(S) 2- (2-iodophenyl) pyrrolidine is an organic compound with a wide range of uses in the field of organic synthesis.
First, this compound is often used as a key intermediate to construct complex natural products and bioactive molecules. Due to its unique molecular structure, the presence of pyrrolidine rings and iodophenyl groups endows it with specific reactivity and spatial configuration, which can be achieved by many organic reactions, such as coupling reactions, nucleophilic substitution reactions, etc., to construct carbon-carbon bonds and carbon-heteroatomic bonds, thus establishing the basic framework of target molecules. For example, in the construction of alkaloids with specific pharmacological activities, (S) 2- (2-iodophenyl) pyrrolidine can be used as an important starting material. Through ingeniously designed reaction routes, other functional groups can be gradually introduced, and finally the target product can be synthesized.
Second, it also has important applications in the field of medicinal chemistry. It can be used as a lead compound for structural modification and optimization to develop new drugs with higher activity, selectivity and lower toxic and side effects. Studies have shown that compounds containing pyrrolidine structures often have good biocompatibility and receptor affinity, while the introduction of iodine atoms can regulate the electron cloud density and lipid solubility of molecules, which in turn affect the interaction between drugs and targets. For example, some anticancer drugs designed and synthesized on the basis of (S) 2- (2-iodophenyl) pyrrolidine have shown significant inhibition of tumor cell proliferation in vitro and in vivo experiments.
Third, in the field of materials science, (S) 2- (2-iodophenyl) pyrrolidine can be used to prepare functional materials. With its reactivity, it can be introduced into the structure of polymer materials to endow the materials with unique photoelectric properties, thermal stability or mechanical properties. For example, when preparing organic Light Emitting Diode (OLED) materials, introducing the compound as a functional unit into the polymer backbone is expected to improve the luminous efficiency and stability of the material, thereby improving the performance of OLED devices.
What are the synthesis methods of (s) 2- (2-iodophenyl) pyrrolidine?
There are various ways to synthesize (S) -2 - (2 -iodophenyl) pyrrolidine. One is to use suitable starting materials and borrow the delicate combination of organic chemical reactions. The benzene ring-containing compound can be taken first, and it can be reacted with halogenating reagents to introduce iodine atoms into the benzene ring at a specific position. This halogenation step requires fine regulation of the reaction conditions, such as temperature, solvent, and reactant ratio, to ensure that the iodine atoms are precisely connected to the target check point.
Then, the pyrrolidine ring system is constructed. The cyclization process can be initiated by reacting the nitrogen-containing compound with a suitable electrophilic reagent. This cyclization reaction also requires careful selection of reaction conditions in order to proceed in the desired direction to generate the desired pyrrolidine structure. In this process, it is necessary to pay attention to the control of stereochemistry to obtain the target product (S) -configuration.
Another strategy is to construct a pyrrolidine precursor first, and then modify the benzene ring. Pyrrolidine compounds are synthesized first, and then iodine atoms are introduced into the benzene ring by halogenation or other substitution reactions. However, this path also needs to strictly control the conditions of each step of the reaction to ensure the smooth progress of the reaction and the purity of the product meets the requirements.
Furthermore, the reaction catalyzed by transition metals can be used. Transition metal catalysts can effectively promote the formation and fracture of various chemical bonds. In the synthesis of this compound, it may be used to catalyze the reaction of halogenated aromatics with nitrogen-containing nucleophiles, so as to achieve the synthesis of (S) -2 - (2 -iodophenyl) pyrrolidine in one or more steps. Although this method has the potential for high efficiency, it also has strict requirements on the selection and dosage of catalysts, the pH of the reaction system and other conditions. In short, the synthesis of this compound requires careful consideration of many factors such as the availability of raw materials, the difficulty of controlling the reaction conditions, and the yield and purity of the product, and the reaction route is carefully designed.
What are the physical properties of (s) -2- (2-iodophenyl) pyrrolidine?
(S) -2 - (2 - iodophenyl) pyrrolidine is an organic compound. Its physical properties are quite important, and it is related to many uses and reaction characteristics of this compound.
Looking at its physical state, under room temperature and pressure, (S) -2 - (2 - iodophenyl) pyrrolidine is usually in a liquid state, with a relatively uniform texture and good fluidity. Its color may be colorless to light yellow, with good transparency. If placed in a transparent container, it can be clearly seen.
When it comes to odor, this compound may have a certain special smell, but its taste is not pungent and unpleasant, but it also needs to be disposed of in a suitable ventilated environment to avoid odor accumulation.
The melting point and boiling point of (S) -2 - (2-iodophenyl) pyrrolidine are also key physical properties. The melting point is related to the temperature limit of its transition from solid to liquid; the boiling point is the critical temperature of the transition from liquid to gas. The melting point is measured experimentally in a specific temperature range, and the boiling point also has corresponding values, which depend on the structure of the compound and the intermolecular forces.
Furthermore, the solubility cannot be ignored. Among common organic solvents, (S) -2 - (2-iodophenyl) pyrrolidine may exhibit good solubility and can be miscible with some organic solvents, but its solubility in water may be limited. This property makes it necessary to choose the solvent reasonably according to its solubility during separation, purification and reaction operations.
In addition, the density is the mass per unit volume of the substance, and the density of (S) -2 - (2-iodophenyl) pyrrolidine is also one of its inherent physical properties. It is of great reference value for material measurement in related chemical production and experimental operations.
What is the market outlook for (s) -2- (2-iodophenyl) pyrrolidine?
(S) -2 - (2 -iodophenyl) pyrrolidine is also an organic compound. Looking at its market prospects, it can be analyzed from the supply and demand ends and technological progress.
In terms of demand, this compound is often a key intermediate in the field of medicinal chemistry. In the process of many innovative drug development, its unique structure can be chemically modified to meet the needs of specific targets and help create new drugs. With the increasing global demand for innovative drugs, especially in the research and development of anti-cancer and neurological drugs, the demand for (S) -2 - (2 -iodophenyl) pyrrolidine may be on the rise. And in the fine chemical industry, it can be used to prepare materials with special properties, such as optically active materials. With the development of electronics, display and other industries, the demand for related materials may also promote its market growth.
In terms of supply, the method of preparing this compound in the past may have cumbersome steps and low yield. However, today, chemical synthesis technology has advanced, and new synthesis paths are constantly emerging. For example, the application of new catalytic reactions can make synthesis more efficient and green. In this way, production costs may drop, production scale can be expanded, and market supply can also be gradually enriched.
However, its market prospects are not without challenges. The synthesis process may involve expensive reagents and complex conditions, and some technologies may have patent barriers, restricting production and promotion. And similar alternative compounds also pose a competitive threat to its market share.
In summary, (S) -2 - (2 -iodophenyl) pyrrolidine has broad market prospects due to the demand in the fields of medicine and fine chemicals. To fully tap its potential, it is still necessary for scientific research and industry to work together to overcome the technical and cost constraints in order to cope with the competition.