19255-03-9

Usage

Structure

Heptadiene backbone with a chlorine atom and a propenyl group attached at the fourth carbon

Explanation

The compound has a chain of seven carbon atoms (heptadiene) with two carbon-carbon double bonds. A chlorine atom is attached to the fourth carbon, and a propenyl group (a three-carbon chain with a double bond at one end) is also attached to the fourth carbon.

Explanation

The compound contains alkene functional groups (carbon-carbon double bonds), an allylic chloride (a chlorine atom attached to a carbon in an allylic position, i.e., adjacent to a double bond), and an allyl group (a propenyl group).

Explanation

Due to its unique structure, 1,6-Heptadiene, 4-chloro-4-(2-propenyl)can be used as a starting material or intermediate in the production of a wide range of organic chemicals and polymers.

Explanation

The compound's structure and functional groups make it a potential precursor for the development of pesticides and herbicides, which are used to control pests and weeds in agriculture.

Explanation

The presence of the chlorine atom and propenyl group in the molecule allows for the creation of various chemical compounds with different properties and applications by undergoing further chemical reactions.

Explanation

Most organic compounds with a molecular weight similar to 1,6-Heptadiene, 4-chloro-4-(2-propenyl)are liquids at room temperature. However, the exact physical state would depend on the specific conditions and purity of the compound.

Explanation

The presence of alkenes, allylic chlorides, and allyl groups in the molecule makes it highly reactive and prone to undergoing various chemical reactions, such as addition, substitution, and elimination reactions.

Explanation

As with many chemicals, 1,6-Heptadiene, 4-chloro-4-(2-propenyl)may pose health and environmental risks if not handled and disposed of properly. It is essential to follow safety guidelines and regulations when working with 1,6-Heptadiene, 4-chloro-4-(2-propenyl)-.

Explanation

Due to its nonpolar nature and the presence of hydrocarbon chains, 1,6-Heptadiene, 4-chloro-4-(2-propenyl)is expected to be soluble in organic solvents like hexane, toluene, and ethyl acetate. However, its solubility in water is likely low due to its hydrophobic nature.

Functional Groups

Alkene, Allylic Chloride, and Allyl

Applications

Intermediate in the synthesis of various organic chemicals and polymer materials

Agricultural Applications

Precursor to pesticides and herbicides

Versatility

Building block for diverse chemical compounds

Physical State

Likely a liquid at room temperature

Reactivity

Reactive due to the presence of multiple functional groups

Hazards

Potential health and environmental risks

Solubility

Likely soluble in organic solvents