Iupac Name | (1S,3R)-3-(2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropane-1-carbonyl chloride |
Molecular Formula | C10H10Cl2F3O |
Molecular Weight | 275.085 g/mol |
Physical State | Likely liquid or solid (predicted from structure, no data) |
Solubility | Expected to be soluble in non - polar to moderately polar organic solvents |
Vapor Pressure | Low (due to cyclic and polar functional groups) |
Chemical Name | (1S,3R)-3-(2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropane-1-carbonyl chloride |
Molecular Formula | C10H10Cl2F3O |
Molecular Weight | 275.09 |
Name | (1S,3R)-3-(2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropane-1-carbonyl chloride |
Molecular Formula | C10H10Cl2F3O |
Molar Mass | 275.085 g/mol |
Physical State | Likely liquid or solid at room temperature |
Reactivity | Reactive due to the presence of carbonyl chloride group (can react with nucleophiles like amines, alcohols) |
Chirality | Chiral compound with (1S,3R) configuration |
Chemical Name | (1S,3R)-3-(2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropane-1-carbonyl chloride |
Molecular Formula | C10H10Cl2F3O |
Molecular Weight | 275.085 g/mol |
What is the chemical structure of (1S, 3R) -3- (2-chloro-3,3,3-trifluoroprop-1-en-1-yl) -2, 2-dimethylcyclopropane-1-carbonyl chloride?
This is the nomenclature of an organic compound. To clarify its chemical structure, it is necessary to gradually analyze it according to the system nomenclature. " (1S, 3R) -" indicates the three-dimensional configuration of the compound. "1S" refers to the configuration of the carbon atom at the 1st position of the compound as S type, and the configuration of the carbon atom at the 3rd position of the table of "3R" is R type. "3- (2-chloro-3,3,3-trifluoropropyl-1-ene-1-yl) ", it can be seen that there is a substituent at the 3rd position of cyclopropane, which is an unsaturated hydrocarbon group containing chlorine and fluorine. " 2,2-Dimethylcyclopropane-1-carbonyl chloride ", indicating that the parent is cyclopropane, with two methyl groups at the 2nd position and carbonyl chloride at the 1st position.
Overall, its chemical structure is cyclopropane as the parent, with carbonyl chloride at the 1st position, two methyl groups at the 2nd position, and 3-position (2-chloro-3,3,3-trifluoropropane-1-ene-1-yl). Cyclopropane has a unique three-membered ring structure, with high activity of carbonyl chloride, and unsaturated hydrocarbon groups containing chlorine and fluorine also affect the properties of compounds. The structure of this compound determines that it may participate in specific organic reactions and may have important uses in the field of organic synthesis.
What are the physical properties of (1S, 3R) -3- (2-chloro-3,3,3-trifluoroprop-1-en-1-yl) -2, 2-dimethylcyclopropane-1-carbonyl chloride?
(1S, 3R) - 3- (2-chloro-3,3,3-trifluoropropane-1-ene-1-yl) - 2,2-dimethylcyclopropane-1-formyl chloride, an organic compound. Its physical properties are crucial for the behavior and application of this compound in various scenarios.
Looking at its properties, under normal circumstances, (1S, 3R) -3- (2-chloro-3,3,3-trifluoropropane-1-ene-1-yl) -2,2-dimethylcyclopropane-1-formyl chloride or a colorless to light yellow liquid has a clear appearance and certain fluidity. This appearance characteristic may be related to the interaction between atoms in the molecular structure and the intermolecular forces.
Discusses the boiling point. Due to the presence of functional groups such as chlorine atoms and trifluoromethyl in the molecule, these groups enhance the intermolecular interaction force, making its boiling point or relatively high. Specifically, under standard atmospheric pressure, its boiling point may be within a certain range, but the exact value needs to be accurately determined experimentally. A higher boiling point means that during the heating process, more energy needs to be supplied to make it change from liquid to gaseous state. In terms of the melting point, the molecular structure of the compound has a certain rigidity, and the presence of cyclopropane structures and substituents such as dimethyl affects the arrangement and accumulation of molecules. Its melting point may be in a specific temperature range, and this temperature range also needs to be precisely determined by experiments. The melting point is defined for the solid-liquid transition conditions of the compound, which is related to its physical state at different temperatures.
In terms of solubility, in view of the fact that there are both lipophilic cyclopropane and dimethyl parts in the molecule, as well as chlorine and fluorine-containing polar groups, this compound may have certain solubility in some organic solvents, such as common halogenated hydrocarbon solvents such as dichloromethane and chloroform. Due to the principle of similarity and miscibility, the structure of halogenated hydrocarbons and this compound has a certain similarity, which is conducive to mutual dissolution. However, the solubility in water may be poor, because the hydrophobic part of the molecule as a whole accounts for a large proportion, and it is difficult to form effective interactions with water molecules.
Density is also one of its important physical properties. Due to the existence of relatively large atomic weights such as chlorine and fluorine in the molecule, the density of this compound may be relatively large, which is The accurate determination of its density is of great significance for the accurate measurement and control of the amount of reactant in the process of chemical production and experimental operation.
What is the synthesis method of (1S, 3R) -3- (2-chloro-3,3,3-trifluoroprop-1-en-1-yl) -2, 2-dimethylcyclopropane-1-carbonyl chloride?
The synthesis of (1S, 3R) -3- (2-chloro-3,3,3-trifluoropropane-1-ene-1-yl) -2,2-dimethylcyclopropane-1-formyl chloride is a challenging issue in the field of organic synthesis. To prepare this product, the following ancient method can be followed:
First select a suitable cyclopropane derivative, which needs to contain a modifiable group at a specific location to facilitate subsequent reactions. The cyclopropane derivative is placed in a suitable reaction vessel, accompanied by a precisely prepared reaction solvent that can effectively dissolve the reactants without adversely affecting the reaction process.
Then, a reagent containing chlorine and trifluoromethyl is slowly added. This reagent should be added in a delicate ratio, and the addition process requires strict control of the reaction temperature and reaction time. The control of temperature is particularly critical. If it is too high, the reaction will be out of control, and if it is too low, the reaction will be delayed. At this stage, a nucleophilic substitution or addition reaction will occur in the reaction system, so that 2-chloro-3,3,3-trifluoropropane-1-ene-1-group is introduced on the cyclopropane derivative.
After the above reaction is completed, the reaction product needs to be separated and purified. Classic separation methods such as column chromatography and recrystallization can be used to obtain high-purity intermediates.
Then, for this intermediate product, an acid chloride group is introduced. Select a suitable chlorination reagent, such as dichlorosulfoxide, and react with the intermediate product under specific conditions. This reaction also requires careful regulation of temperature, time and the proportion of reactants to ensure the smooth conversion of carbonyl to acid chloride, resulting in (1S, 3R) -3- (2-chloro-3,3,3-trifluoropropane-1-ene-1-yl) -2,2-dimethylcyclopropane-1-formyl chloride. Each step of the reaction requires fine operation, and the control of the reaction conditions must be weighed like a scale, and every detail must be checked to obtain the ideal product.
What are the application fields of (1S, 3R) -3- (2-chloro-3,3,3-trifluoroprop-1-en-1-yl) -2, 2-dimethylcyclopropane-1-carbonyl chloride?
(1S, 3R) -3- (2-chloro-3,3,3-trifluoropropane-1-ene-1-yl) -2,2-dimethylcyclopropane-1-formyl chloride, which has a wide range of uses. In the field of pharmaceutical creation, it can be used as a key intermediate. Through exquisite chemical reactions, it can be integrated into complex molecular structures to develop novel and specific drugs. Due to its unique chemical structure, it may endow the prepared drugs with special biological activities, such as targeting specific biomolecules and accurately acting on the focus, providing a new way to overcome difficult diseases. < Br >
In the field of materials science, this compound is also promising. It participates in the process of material synthesis, or can improve the properties of materials. For example, introducing it into the synthesis of polymer materials can optimize the stability, weather resistance and chemical resistance of materials, so that materials can maintain excellent properties in extreme environments, and make great use of materials in fields such as aerospace and automobile manufacturing.
In the field of fine chemicals, as an important chemical raw material, fine chemicals with special functions can be prepared through a series of reactions. For example, by synthesizing special structures of fragrances to give products a unique and lasting aroma, or by preparing high-performance paint additives to enhance the adhesion, wear resistance, and other properties of coatings, they are widely used in home decoration, industrial equipment painting, and other industries.
What is the safety of (1S, 3R) -3- (2-chloro-3,3,3-trifluoroprop-1-en-1-yl) -2 2-dimethylcyclopropane-1-carbonyl chloride?
(1S, 3R) - 3- (2-chloro-3,3,3-trifluoropropane-1-ene-1-yl) - 2,2-dimethylcyclopropane-1-formyl chloride, this is an organic compound. In terms of its safety, it should be viewed from many aspects.
First of all, the physical properties of this substance may have a certain volatility. If it evaporates in the air, it can cause cough, asthma and other diseases after inhalation, or irritate the respiratory tract. When it is a liquid, it may have a certain fluidity. If it accidentally touches the skin, or corrodes the skin due to chemical action, it will cause redness, swelling, pain, and even ulceration. If splashed into the eye, because of its chemical activity, or cause serious damage to the eye tissue, affecting vision.
Looking at the chemical properties, it contains chlorine atoms and carbonyl groups, and its chemical properties are active. In contact with water or moisture, or hydrolysis reactions occur, generating corrosive gases such as hydrogen chloride, which not only pollutes the environment, but also has strong irritation to the respiratory tract, eyes and noses and other organs of the surrounding personnel. In case of alkali substances, or a violent reaction occurs, causing heat release. If it is in a limited space, or it is dangerous due to heat accumulation. Encounter with strong oxidants, or due to redox reactions, violent reactions or even explosions.
Because of its fluorine atoms, some fluorine-containing organic compounds have high stability and are difficult to degrade in the environment, or cause environmental pollution. In living organisms, or due to bioaccumulation, it is passed along the food chain and affects biological health.
In summary, (1S, 3R) - 3- (2-chloro-3,3,3-trifluoropropyl-1-ene-1-based) - 2,2-dimethylcyclopropane-1-formyl chloride is not safe. When using, storing and transporting, it is necessary to follow strict operating procedures and take protective measures to reduce risks.