Benzenebutanenitrile, also known as 4-phenylbutyronitrile, is an organic compound characterized by its structure, which features a butyronitrile chain attached to a phenyl group. Its molecular formula is C11H12N, indicating the presence of carbon, hydrogen, and nitrogen atoms. This compound typically appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. Benzenebutanenitrile is known for its moderate polarity, which allows it to dissolve in various organic solvents while being less soluble in water. It has applications in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals, due to its ability to serve as a building block in chemical reactions. The compound's properties, such as boiling point and melting point, can vary based on the specific conditions and purity levels. Safety precautions should be taken when handling this substance, as it may pose health risks if inhaled or ingested. Overall, benzenebutanenitrile is a versatile compound with significant relevance in chemical research and industrial applications.

Benzenebutanenitrile

2046-18-6: (3-Cyanopropyl)benzene, 1-Cyano-3-phenylpropane, 4-Phenylbutanenitrile, Benzenebutanenitrile, Butyronitrile, 4-phenyl-, NSC 1853, Phenylbutyronitrile, γ-Phenylpropyl cyanide, 4-Phenylbutyronitrile

4-Phenylbutanenitrile

4-Phenylbutyronitrile is a chemical compound that is used in the production of styrene. It is a byproduct of the reaction between chlorobenzene and acetaldehyde, which also produces acrylonitrile. 4-Phenylbutyronitrile can be found as an environmental pollutant in water and soil due to its high reactivity with iron oxides and organic solvents. 4-Phenylbutyronitrile has been shown to inhibit enzymes such as oxidases, hydrolases, and transferases. The profile of this compound has been determined using liquid chromatography coupled with mass spectrometry (LCMS). 4-Phenylbutyronitrile has a crystalline structure that consists of alternating benzene rings and nitrile groups. The synthesis of 4-phenylbutyronitrile can be achieved through the reaction of phenylacetonitrile with hydrogen cyanide over copper or nickel

CAS 2046-18-6: Benzenebutanenitrile

4-Phenylbutanenitrile

Ref: 10-F679431

4-Phenylbutyronitrile

Ref: 3D-CAA04618

4-Phenylbutyronitrile

Ref: 3B-P1025

Benzenebutanenitrile

Ref: IN-DA0029LN

4-Phenylbutanenitrile

Ref: 54-OR1023686