1,3,5-Cyclohexanetricarbonitrile, with the CAS number 183582-92-5, is a chemical compound characterized by its cyclic structure and the presence of three cyano (–C≡N) groups attached to a cyclohexane ring. This compound is typically a solid at room temperature and exhibits a crystalline appearance. The presence of multiple cyano groups contributes to its potential reactivity, making it a subject of interest in various chemical applications, including organic synthesis and materials science. The cyano groups can participate in nucleophilic reactions and can also influence the compound's solubility and polarity. Additionally, 1,3,5-cyclohexanetricarbonitrile may exhibit interesting thermal and chemical stability, which can be advantageous in specific industrial processes. Its unique structure and functional groups may also allow for the formation of polymers or coordination complexes, expanding its utility in advanced materials and chemical research. As with many nitriles, safety precautions should be taken when handling this compound due to potential toxicity and environmental concerns.

1,3,5-CYCLOHEXANETRICARBONITRILE

183582-92-5: 1,3,5-Tricyanocyclohexane, (1alpha,3alpha,5alpha)-1,3,5-Cyclohexanetricarbonitrile, (1alpha,3alpha,5alpha)-1,3,5-Tricyanocyclohexane, Cyclohexane-1,3,5-Tricarbonitrile,  1,3,5-Cyclohexanetricarbonitrile

1,3,5-Cyclohexanetricarbonitrile (cis- and trans- mixture) is an organic compound that is a trimethylcyclohexane derivative. It has absorption spectroscopy in the region of 230 to 280 nanometers. The cis- and trans- forms of this molecule have been shown to have different profiles with respect to carboxylate, gel permeation chromatography, photoelectron spectroscopy, and molecular size. The cis form is less soluble in water than the trans form. This difference in solubility can be attributed to the difference in hydrogen bonding between the two forms. In addition, 1,3,5-Cyclohexanetricarbonitrile (cis- and trans- mixture) has stereoisomers with different functional theory for their reactions with anions such as chloride and bromide which are due to steric hindrance from methyl groups on adjacent carbons.

CAS 183582-92-5: 1,3,5-CYCLOHEXANETRICARBONITRILE

1,3,5-Cyclohexanetricarbonitrile (cis- and trans- mixture)

Ref: 3D-IHA58292

1,3,5-Cyclohexanetricarbonitrile

Ref: IN-DA0027PU

1,3,5-Cyclohexanetricarbonitrile (cis- and trans- mixture)

Ref: 3B-C2327