2-Butyl-7-chloro-1H-indene is an organic compound characterized by its indene structure, which consists of a fused benzene and cyclopentene ring. The presence of a butyl group at the 2-position and a chlorine atom at the 7-position contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid, exhibiting moderate volatility and solubility in organic solvents. Its molecular structure suggests potential reactivity, particularly in electrophilic substitution reactions due to the electron-rich indene system. The chlorine substituent can also influence the compound's reactivity and stability, making it a candidate for various synthetic applications in organic chemistry. Additionally, the presence of the butyl group may enhance hydrophobic characteristics, affecting its interactions in biological systems and its potential use in pharmaceuticals or agrochemicals. Safety data should be consulted for handling and exposure guidelines, as halogenated compounds can pose environmental and health risks.

2-Butyl-7-chloro-1H-indene

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2-Butyl-7-chloro-1H-indene (2BCI) is a heterocycle, which is also known as an ethenylbenzene. This compound has been shown to have vasomotor symptoms and monoamine reuptake inhibition effects. 2BCI was found to be effective in treating diabetic neuropathy, and it may act by inhibiting cardiac function. 2BCI inhibits the reuptake of serotonin and dopamine by binding to the transporter proteins that are responsible for removing these neurotransmitters from synapses. In addition, this compound is used as a diluent for nitroaromatic explosives, such as TNT and RDX, because it reduces the sensitivity of nitroaromatic compounds to shock and friction. 2BCI can also be used as a carboxyalkylating agent or an alkylating agent in organic synthesis. It reacts with halides or cyclopropanes to form carboxylic acids

CAS 1003709-15-6: 2-Butyl-7-chloro-1H-indene

2-Butyl-7-chloro-1H-indene

Ref: 3D-DQB70915

1H-Indene, 2-butyl-7-chloro-

Ref: IN-DA0001S5