5-Fluoro-1-pentyne is an organic compound characterized by its alkyne functional group, specifically a terminal alkyne due to the presence of a triple bond between the first and second carbon atoms in the pentane chain. The molecular formula for 5-fluoro-1-pentyne is C5H7F, indicating it contains five carbon atoms, seven hydrogen atoms, and one fluorine atom. This compound is typically a colorless liquid at room temperature and exhibits a distinct odor. Its fluorine substituent can influence its reactivity and physical properties, making it of interest in various chemical applications, including synthesis in organic chemistry and potential use in pharmaceuticals. The presence of the triple bond contributes to its unsaturation, which can lead to increased reactivity compared to saturated hydrocarbons. Additionally, 5-fluoro-1-pentyne may participate in various chemical reactions, such as nucleophilic additions or coupling reactions, due to the presence of both the alkyne and the fluorine atom. Safety precautions should be taken when handling this compound, as it may pose health risks.

5-Fluoro-1-pentyne

764-36-3: 5-Fluoro-1-pentyne is an organic compound characterized by its alkyne functional group, specifically a terminal alkyne due to the presence of a triple bond between the first and second carbon atoms in the pentane chain. The molecular formula for 5-fluoro-1-pentyne is C5H7F, indicating it contains five carbon atoms, seven hydrogen atoms, and one fluorine atom. This compound is typically a colorless liquid at room temperature and exhibits a distinct odor. Its fluorine substituent can influence its reactivity and physical properties, making it of interest in various chemical applications, including synthesis in organic chemistry and potential use in pharmaceuticals. The presence of the triple bond contributes to its unsaturation, which can lead to increased reactivity compared to saturated hydrocarbons. Additionally, 5-fluoro-1-pentyne may participate in various chemical reactions, such as nucleophilic additions or coupling reactions, due to the presence of both the alkyne and the fluorine atom. Safety precautions should be taken when handling this compound, as it may pose health risks.

Stability Volatile Applications 5-Fluoro-1-pentyne use as a reactant/reagent for preparation of glutamic acid-based peptidomimetic prostate-specific membrane antigen binding agents for imaging use. References Wang, E., et al.: PCT Int. Appl., WO 2013028664 A1 20130228 (2013)

CAS 764-36-3

5-Fluoro-1-pentyne

5-Fluoro-1-pentyne

Ref: TR-F593648

5-Fluoro-1-pentyne

Ref: 3D-AAA76436