Tert Butyl 6 Cyano 2 2 4 Ethyl 3 Iodophenyl Propan 2 Yl 1h Indole 3 Carboxylate

Ugh! This is the name of an organic compound. To know its chemical structure, you need to analyze its name in detail. "Tert-butyl", tert-butyl is also a branched chain alkyl group containing four carbons. "6-cyano" Epiindole ring has a cyano group at the 6th position. " 2 - (2 - (4 - ethyl - 3 - iodophenyl) propan - 2 - yl) ", this long chain part, first look at" (4 - ethyl - 3 - iodophenyl) ", that is, 4 - ethyl - 3 - iodophenyl, is connected to the second position of the propyl group, which in turn is connected to the second position of the indole ring." 1H - indole - 3 - carboxylate "indicates that this is an indole - 3 - carboxylate structure, and the tert-butyl group is attached to the oxygen atom of the ester group.
In summary, the chemical structure of the compound is an indole ring as the core, with a cyano group at 6 positions, a complex side chain at 2 positions, a propyl group containing 4-ethyl-3-iodophenyl, and a carboxylic acid tert-butyl ester at 3 positions. Such a structure may have unique properties and uses in the fields of organic synthesis and medicinal chemistry, and needs to be investigated in detail according to experiments and theoretical calculations.

Tert-butyl 6-cyano-2- (2- (4-ethyl-3-iodophenyl) propyl-2-yl) -1H-indole-3-carboxylic acid ester is an organic compound. Its main uses are diverse, and it is often used as a key intermediate in the field of organic synthesis. Gain This compound is rich in a variety of active functional groups, such as cyano, ester and indole rings. These functional groups can participate in the construction of more complex organic molecular structures through various chemical reactions, such as nucleophilic substitution, addition reactions, etc., to assist in the synthesis of compounds with specific biological activities or material properties.
In the field of medicinal chemistry, such compounds containing indole structures have attracted much attention. Indole rings are the core structural units of many bioactive natural products and drug molecules, or have potential biological activities, such as anti-tumor, anti-inflammatory, and antibacterial. Tert-butyl 6-cyano-2- (2- (4-ethyl-3-iodophenyl) propyl-2-yl) -1H-indole-3-carboxylic acid esters may be optimized as lead compounds, and new therapeutic drugs may be developed through structural modification and activity screening.
In the field of materials science, this compound may exhibit unique optoelectronic properties due to its special structure. For example, it can be used to prepare organic optoelectronic materials and play a role in organic Light Emitting Diodes (OLEDs), organic solar cells and other devices. The molecular structure regulates the optical and electrical properties to improve the performance of materials and devices.

Alas! To prepare Tert - butyl 6 - cyano - 2 - (2 - (4 - ethyl - 3 - iodophenyl) propan - 2 - yl) -1H - indole - 3 - carboxylate, the synthesis method is roughly as follows.
First, a suitable starting material can be found. Based on 4 - ethyl - 3 - iodobenzene, an appropriate functional group can be introduced to react with a reagent containing a propyl structure to construct a 2 - (4 - ethyl - 3 - iodophenyl) propan - 2 - yl fragment. In this process, it may be necessary to select suitable reaction conditions, such as suitable solvents and alkalis, to promote the smooth progress of the reaction and obtain high-yield products.
times, connect this fragment to the compound containing indole structure. It can be used by common reactions in organic synthesis, such as nucleophilic substitution, coupling reaction, etc. If nucleophilic substitution is used, it is necessary to pay attention to the selectivity of the reaction check point, so that the reaction precisely occurs at the second position of indole.
After the intermediate of 2- (2 - (4 - ethyl - 3 - iodophenyl) propan - 2 - yl) -1H - indole is obtained, the cyanide group is introduced at the 6th position. This step may require the use of a specific cyanide reagent to control the reaction conditions and prevent the growth of side reactions. At the end of
, the tert-butyl carboxylic acid ester group is introduced at the 3rd position. This goal can be achieved by reacting with tert-butyl carbonate reagents under suitable catalytic conditions. After each step of the reaction, the product needs to be properly separated and purified, and the purity of the product needs to be ensured by recrystallization and column chromatography to lay a good foundation for the next reaction. Therefore, sequential operation may result in the synthesis of this compound.

Alas! This is tert-butyl 6-cyano-2- (2- (4-ethyl-3-iodophenyl) propyl-2-yl) -1H-indole-3-carboxylic acid ester. This compound has many physical and chemical properties.
In terms of its solubility, its structure contains hydrophobic tert-butyl, aromatic ring and cyano and ester groups with certain polarities. It should have good solubility in organic solvents such as dichloromethane, chloroform and tetrahydrofuran, because such solvents can be miscible with the compound by means of Van der Waals force, dipole-dipole interaction, etc. However, the solubility in water is not good, because the hydrophobic part accounts for a large proportion, it is difficult to form an effective interaction with water.
Looking at its melting point, due to the existence of van der Waals force and dipole-dipole interaction between molecules, and cyano and ester groups can participate in the formation of hydrogen bonds, enhancing the intermolecular force, causing its melting point to be not low. However, the specific value needs to be accurately determined by experiments.
When it comes to stability, the aromatic ring structure makes it have a certain conjugate stability, but the iodine atom has a large atomic radius and a weak C-I bond. Under certain conditions, such as light, heating or encountering nucleophiles, the C-I bond may break, triggering a chemical reaction and affecting its stability. The chemical properties of cyanyl groups are more active, and reactions such as hydrolysis and addition can occur, which also affects their stability. Ester groups can be hydrolyzed under the catalysis of acids or bases, so they are not stable in acid-base environments.
In terms of polarity, because cyanyl and ester groups are polar groups, aromatic rings and alkyl groups are non-polar parts, and the whole is a certain polarity. This polarity affects its chromatographic behavior and interactions with other substances.

I don't know the price range of "Tert-butyl + 6 - cyano - 2 - (2 - (4 - ethyl - 3 - iodophenyl) propan - 2 - yl) -1h - indole - 3 - carboxylate" on the market. This compound may be dedicated to a specific field, and its price is affected by many factors.
First, the difficulty of synthesis has a great impact. If the synthesis requires complicated steps, rare raw materials, or strict requirements on reaction conditions, the cost will be high, and the price will be expensive. If the synthesis requires dozens of steps of reaction, and some of the raw materials are rare, the preparation process requires precise temperature control, pressure control, and special catalysts, the cost will increase greatly, and the price will be high.
Second, the amount of market demand is also the key. If there is strong demand in fields such as pharmaceutical research and development, materials science, and limited supply, the price will rise according to the reason of supply and demand. On the contrary, if there is little demand, the price may tend to be easy.
Third, the level of purity is also related to the price. For high purity, preparation is more difficult, more resources are required, and the price is often far higher than that of low purity. For example, for high-end scientific research experiments, extremely high purity is required, and the price is naturally high.
Fourth, the price varies depending on the manufacturer. Well-known large factories may have high prices due to strict brand reputation and quality control; while small factories may compete at low prices if they do not have brand and quality advantages.
However, I have not heard of its exact price range in the market, and it is difficult to know its price. If you want to know the price of this product, you can only get clues if you consult chemical raw material suppliers, scientific research reagent sellers, or relevant professional trading platforms.