80935-59-7

Basic information

• Product Name: 2,2',2''-(benzene-1,3,5-triyl)triacetonitrile
• Synonyms: 2,2',2''-(benzene-1,3,5-triyl)triacetonitrile
• CAS NO: 80935-59-7
• Molecular Weight: 195.224
• Mol File: 80935-59-7.mol

Chemical Properties

• CAS DataBase Reference: 2,2',2''-(benzene-1,3,5-triyl)triacetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2',2''-(benzene-1,3,5-triyl)triacetonitrile(80935-59-7)
• EPA Substance Registry System: 2,2',2''-(benzene-1,3,5-triyl)triacetonitrile(80935-59-7)

Safety Data

• Hazardous Substances Data: 80935-59-7(Hazardous Substances Data)

Usage

Uses

Used in Organic Chemistry:
2,2',2''-(Benzene-1,3,5-triyl)triacetonitrile is utilized as a synthetic building block for the creation of various complex organic molecules. Its structural properties allow for the development of diverse chemical entities, contributing to the advancement of organic chemistry.
Used in Materials Science:
In the realm of materials science, 2,2',2''-(benzene-1,3,5-triyl)triacetonitrile is explored for its potential in the development of novel organic materials. Its unique characteristics are being studied to enhance the properties of these materials, potentially leading to breakthroughs in material applications.
Used in Pharmaceutical Research:
2,2',2''-(Benzene-1,3,5-triyl)triacetonitrile has been investigated for its potential biological activities, such as antitumor and antimicrobial properties. While further research is necessary to fully understand its capabilities and applications in this field, its current studies indicate a promising direction for future pharmaceutical and medical uses.

Upstream product

• 17299-97-7 α,α',α''-trichloromesitylene 
• 18226-42-1 1,3,5-Tris(bromomethyl)benzene 
• 4435-67-0 1,3,5-benzenetriacetic acid 
• 2672-58-4 1,3,5-tris-(methoxycarbonyl)benzene 
• 4464-18-0 1,3,5-tris(hydroxymethyl)benzene 
• 143-33-9 sodium cyanide 

Downstream Products

• 18226-47-6 1,3,5-tris(2'-bromoethyl)benzene 
• 18226-43-2 1,3,5-benzenetriethanol 
• 351435-98-8 (benzene-1,3,5-triyl)tris(3-phenylacrylonitrile) 
• 1360768-28-0 α,α',α''-tris(hydroxyimino)-1,3,5-benzenetriacetonitrile 

Relevant articles and documents

Preparation method of (benzene-1, 3, 5-triacyl) triacetonitrile

The invention belongs to the technical field of organic synthesis, and particularly relates to a preparation method of (benzene-1, 3, 5-triacyl) triacetonitrile. The reaction reagent is a mixed solvent of DMSO and water, and water is added, so that the solubility of reactants of potassium cyanide is improved, generated potassium chloride and potassium bromide are promoted to enter a water phase intime, the reaction can be carried out in the forward direction, the reaction time is shortened, and the conversion rate of raw materials is remarkably increased; catalytic equivalent organic alkali is added into a reaction system, so that the leaving of halogen ions is promoted, the efficiency of a forward reaction is promoted, and the product is easier to separate and purify; the reaction time is at least shortened by 13-142 hours compared with the reported reaction time, a large amount of time cost is saved, and the efficiency of quantitative production of products is improved; and the preparation process is simple and easy to control, the raw material conversion rate is high, the target product yield is 94.5% or above, the residual quantity of highly toxic substances is obviously reduced, and the experiment safety is improved to the maximum extent.

Corresponding amine nitrile and method of manufacturing thereof (by machine translation)

The present invention relates to a nitrile manufacturing method, which has characteristics of significantly-reduced ammonia source consumption, low environmental pressure, low energy consumption, low production cost, high nitrile purity, high nitrile yield and the like compared with the method in the prior art, wherein nitrile having a complicated structure can be obtained through the method. The present invention further relates to a method for producing a corresponding amine from the nitrile.

Corresponding amine nitrile and method of manufacturing thereof

The invention relates to a preparation method of nitrile. Compared with the prior art, the preparation method has the characteristics of obvious reduction of the usage amount of ammonia sources, low environmental pressure, low energy consumption, low production cost, high purity and yields of nitrile products, and the like, and can be used for obtaining nitrile with a more complex structure. The invention also relates to a method for preparing corresponding amine with nitrile.

Corresponding amine nitrile and method of manufacturing thereof

The invention relates to a preparation method of nitrile. Compared with the prior art, the preparation method has the characteristics of obvious reduction of the usage amount of ammonia sources, low environmental pressure, low energy consumption, low production cost, high purity and yields of nitrile products, and the like, and can be used for obtaining nitrile with a more complex structure. The invention also relates to a method for preparing corresponding amine with nitrile.

Synthesis of bis- and tris(indolinylidenemethyl)benzenes by one-pot reactions of polylithiated nitriles with bis(imidoyl)chlorides of oxalic acid

The reaction of polylithiated di- and tricyanomethylbenzenes with oxalic acid-bis(imidoyl)chlorides afforded novel oligo(indolinylidenemethyl)benzenes with the formation of up to six carbon-carbon bonds. The UV/Vis spectroscopic features of these and related compounds were studied. 1,4-Disubstituted benzenes containing a large π-system have been efficiently prepared by the reaction of dianions with 1,4-dicyanobenzene. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

Synthesis of Macrocyclic (1,3,5)Cyclophane Polylactones

A series of new macrocyclic cyclophane polylactones has been synthesized by one-step condensation of the appropriate tri(acid chloride)s and triols using the silver cyanide-promoted esterification procedure.