1,3-Dichloro-5-propoxybenzene
[CAS# 1202656-18-5]

Identification

• Classification: Organic raw materials >> Aryl compounds
• Name: 1,3-Dichloro-5-propoxybenzene
• Molecular Formula: C₉H₁₀Cl₂O
• Molecular Weight: 205.08
• CAS Registry Number: 1202656-18-5
• SMILES: CCCOC1=CC(=CC(=C1)Cl)Cl

Properties

• Density: 1.2±0.1 g/mL, Calc.^*
• Index of Refraction: 1.522, Calc.^*
• Boiling Point: 259.5±20.0 ºC (760 mmHg), Calc.^*
• Flash Point: 75.2±21.2 ºC, Calc.^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H302-H315-H319-H335
• Precautionary Statements: P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Discovory and Applicatios

1,3-Dichloro-5-propoxybenzene is an organic compound with the molecular formula C9H9Cl2O. It belongs to the class of chlorinated aromatic compounds and features a benzene ring with two chlorine atoms and a propoxy group attached to it. The structure of this compound consists of a propoxy group (-OCH2CH2CH3) attached to the fifth carbon of a dichlorobenzene ring, with the chlorine atoms located at the first and third positions of the ring.

The discovery of 1,3-dichloro-5-propoxybenzene is not attributed to a specific landmark moment in history, as it falls within a class of compounds synthesized through well-known chlorination processes. The compound is typically synthesized through the selective chlorination of propoxybenzene under controlled conditions, with chlorine being introduced to the aromatic ring. Chlorination can be achieved using a variety of reagents such as chlorine gas or other chlorine-containing compounds in the presence of solvents or catalysts.

The applications of 1,3-dichloro-5-propoxybenzene are mainly found within the chemical industry. It is used as a building block in organic synthesis, where it serves as an intermediate in the production of more complex chemicals. Its chlorinated structure makes it useful in the synthesis of other chlorinated compounds, which may have applications in pharmaceuticals, agrochemicals, or materials science. While specific commercial uses for this compound may not be as widespread as other more widely known chlorobenzenes, it is of interest to researchers for the potential it holds in producing functionalized aromatic compounds.

In addition to its synthetic uses, 1,3-dichloro-5-propoxybenzene may also be studied for its potential biological activities, as is the case with many chlorinated aromatic compounds. Chlorinated compounds can exhibit a wide range of properties, such as antimicrobial or anticancer activities, although the specific biological properties of 1,3-dichloro-5-propoxybenzene are less documented in scientific literature.

It is important to note that, like other chlorinated aromatic compounds, 1,3-dichloro-5-propoxybenzene should be handled with care, as exposure to high concentrations of chlorine-based compounds can pose health risks, including skin and eye irritation, and respiratory effects if inhaled. In industrial applications, appropriate safety measures and guidelines should be followed when handling the compound.

In conclusion, 1,3-dichloro-5-propoxybenzene is a chlorinated aromatic compound used primarily in organic synthesis as an intermediate for the production of other chemicals. While it does not have widespread applications on its own, it is valuable within the context of chemical manufacturing and research, where it may be used to create other compounds with diverse industrial and potentially biological applications.