3 1 1 Difluorobut 3 En 1 Yl Quinoxaline 2 Ol
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
3-(1,1-Difluorobut-3-en-1-yl)quinoxaline-2-ol
Chemical Formula C14H12F2N2O
Molar Mass 262.26 g/mol
Appearance Solid (usually)
Solubility In Water Poor (organic compounds often have low water solubility)
Solubility In Organic Solvents Likely soluble in common organic solvents like dichloromethane, chloroform etc.
Uv Vis Absorption Absorption bands characteristic of quinoxaline and double - bond containing groups in the UV - Vis region
Ir Absorption Characteristic peaks for C - F, C = C, N - N, C - N, and O - H bonds
Chemical Formula C14H12F2N2O
Chemical Formula C14H12F2N2O
Chemical Formula C14H12F2N2O
Appearance Solid (predicted)
Solubility In Water Low (predicted)
FAQ

What is the chemical structure of 3- (1,1-difluorobutyl-3-ene-1-yl) quinoxaline-2-ol?

The full name of this substance is more complicated, and its chemical structure is analyzed from the given information "3- (1,1-diethylheptyl-3-alkynyl-1-yl) pentynaldehyde-2-one".

First, the "3- (1,1-diethylheptyl-3-alkynyl-1-yl) " section indicates that a substituent is attached to the third carbon atom of the main chain. This substituent is a heptyne structure with two ethyl substitutions on the first carbon atom of heptyne and a carbon-carbon triple bond on the third carbon atom.

For valeraldehyde-2-keto, "pentyl" indicates that the main chain has 5 carbon atoms, "alkyne" indicates that there is a carbon-carbon triple bond in the molecule, "aldehyde" indicates that there is an aldehyde-CHO at one end of the main chain, and "2-keto" indicates that there is a carbonyl-CO - on the second carbon atom of the main chain.

The substituent is connected to the main chain, and the overall structure surrounds the main chain of valeraldehyde-2-keto. At the third carbon atom, a specific three-bond-containing ethyl-substituted heptyne group is connected. Such a structure makes the compound have multiple chemical properties of alkyne, aldehyde and ketone, the unsaturation of the alkyne bond makes it possible to undergo addition reactions, and the aldehyde group and ketone carbonyl group can also participate in various nucleophilic addition reactions. It has potential application value in the field of organic synthesis and chemistry research.

What are the main uses of 3- (1,1-difluorobutyl-3-ene-1-yl) quinoxaline-2-ol?

3 - (1,1 - diethyl one - 3 - fire - 1 - base) pentyne light - 2 - anise of the main diameter, covered with various.

In "Tiangong Kaiwu", these various materials have their own uses in different processes. Such as the "fire" involved in it, or helpful in the art of smelting and forging. When smelting iron, the control of the fire is related to the quality of iron. This "3 - fire" may be a sign of a specific fire, helping craftsmen to accurately grasp the process of smelting iron, making the texture of iron more refined, making tough tools, indispensable for farming, warfare, etc.

And "1-base" and the like, or play a role in chemical synthesis and other fields. In the art of lacquer making, some raw materials containing specific "bases" can make the color of the paint more bright, and enhance its adhesion and durability. When applied to utensils, it can not only beautify, but also prevent the decay of utensils and prolong its use time.

As for "2-anise", it has a unique nature. In the production of spices, anise can add a unique aroma and adjust the taste of various spices, making the aroma more mellow and pleasant. In the field of medicine, anise also has certain medicinal uses, or can regulate the spleen and stomach, remove cold and relieve pain, and is commonly used by doctors.

"3- (1,1-diethyl-3-fire-1-yl) pentyne light" as a whole or has its uses in the production of optical materials. Or it can be treated by special processes to make optical devices such as lenses, so that when light propagates in them, it presents specific optical effects, or improves the clarity of vision, or is used for precise adjustment of optical instruments. It is of great significance in stargazing and object refinement.

What are the preparation methods of 3- (1,1-difluorobutyl-3-ene-1-yl) quinoxaline-2-ol?

To prepare 3- (1,1-diethylamino-3-alkyne-1-yl) pyridine-2-aldehyde, the following ancient method can be used:

First take an appropriate amount of pyridine derivative as the base, this derivative needs to contain a modifiable check point to facilitate the subsequent introduction of specific groups. In a suitable reaction vessel, put a pyridine derivative, add an appropriate amount of organic solvent, so that the pyridine derivative is fully dissolved to construct a homogeneous reaction environment.

Then, add the reagent containing 1,1-diethylamino-3-alkyne-1-group slowly. This process requires attention to the addition rate to prevent overreaction. After addition, moderate temperature rise will promote the molecular movement of the reaction system to intensify, so as to facilitate the reaction. During this heating stage, the temperature needs to be strictly controlled and maintained at an appropriate range. If it is too high, side reactions will occur frequently, and if it is too low, the reaction rate will be slow.

At the same time, an appropriate amount of catalyst can be added to reduce the activation energy of the reaction and accelerate the reaction process. The amount of catalyst needs to be precisely controlled. Too much or too little will affect the reaction effect. During the reaction, continue to stir to make the reactants fully contact and ensure a uniform reaction.

When the reaction is coming to an end, through careful separation and purification steps, a pure 3- (1,1-diethylamino-3-alkyne-1-yl) pyridine-2-aldehyde can be obtained. This separation and purification, or the method of extraction, is preliminarily separated by the difference in solubility of different solvents to the product and impurities; after column chromatography, according to the difference in the distribution coefficient of the product and impurities between the stationary phase and the mobile phase, further purification is performed to obtain a pure product to meet the needs.

What are the physicochemical properties of 3- (1,1-difluorobutyl-3-ene-1-yl) quinoxaline-2-ol?

3 - (1,1 - diethyl ether - 3 - fire - 1 - yl) pentyne - 2 - alkene physicalization is as follows:

In this compound, its molecules contain a specific functional atomic arrangement. In terms of chemical properties, the presence of diethyl ether groups makes it soluble to a certain extent, soluble in some soluble, because the diethyl ether group has a group that is commonly used in dissolution, can be similar to soluble. And the pentyne - 2 - alkene part, the weight of the alkylene is not and, It has a high reactive activity.

In terms of physical properties, usually under normal conditions, this compound may be liquid. Due to its molecular force, including Vander force, etc., it can hold liquid at an appropriate temperature. Its melt-boiling is affected by molecular effects, and the existence of inconsistencies makes it different from some chemical compounds in the melt-boiling phase. Generally speaking, the higher the degree of inconsistencies, the more difficult the molecular action phase is. The melt-boiling has a certain degree of melting, and the melting may be low. The boiling effect is due to the molecular effect.

In the reaction, the addition of pentyne-2-ene is not the same and the addition is easy to generate inconsistencies. For example, additions can be made to elements, molecules, etc., so that the sum can be changed, and the properties of the molecule can be changed. Its alkynyl moiety may also be used for some specific synthetic reactions, such as some gold compounds, for the construction of more complex molecules. Therefore, the physicalization of this compound is determined by its special molecular properties, which has certain significance in the synthesis of chemical research.

What is the price range of 3- (1,1-difluorobutyl-3-ene-1-yl) quinoxaline-2-ol in the market?

I think your question is about the market price range of 3- (1,1-diene-3-alkyne-1-yl) valyne aldehyde-2-naphthalene. However, this chemical substance is not an ordinary commercial product that I am familiar with, and its price may vary greatly due to various factors such as purity, source, market supply and demand.

If you want to know its exact price, you should consult the firm specializing in chemical reagents, the trading platform of chemical products, or consult with the parties in the industry who are skilled in this field. And these special chemicals are often used in professional fields, and their trading may be restricted by laws and regulations, and must be carried out in accordance with relevant regulations.

In general, it is difficult to determine its price range without detailed details. If you want to know the exact number, you should explore it in detail from the above methods to obtain a rough estimate.