7366-47-4

Basic information

• Product Name: 1,3-Dioxolane, 2-(2-chlorophenyl)-
• CAS NO: 7366-47-4
• Molecular Formula: C9H9ClO2
• Molecular Weight: 184.622
• Mol File: 7366-47-4.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: 1,3-Dioxolane, 2-(2-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxolane, 2-(2-chlorophenyl)-(7366-47-4)
• EPA Substance Registry System: 1,3-Dioxolane, 2-(2-chlorophenyl)-(7366-47-4)

Safety Data

• Hazardous Substances Data: 7366-47-4(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The compound is in a liquid state and has no color.

Explanation

The compound has a mild, pleasant smell.

Explanation

It is used as a starting material or building block in the production of various drugs and chemicals used in agriculture.

Explanation

The compound has the potential to cause changes in the genetic material (DNA) of cells, which can lead to mutations.

Explanation

Exposure to the compound may have negative effects on the reproductive system, potentially causing damage or dysfunction.

Explanation

Due to its potential mutagenic and harmful effects, it is important to follow proper safety protocols when handling this compound to minimize exposure and health risks.

Physical state

Colorless liquid

Odor

Faint, sweet

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Potential mutagen

Yes

Reproductive system effects

Harmful

Safety measures

Handle with caution

Upstream product

• 89-98-5 2-chloro-benzaldehyde 
• 107-07-3 2-chloro-ethanol 
• 7381-30-8 2,2,7,7-tetramethyl-3,6-dioxa-2,7-disilaoctane 
• 107-21-1 ethylene glycol 

Downstream Products

• 1210-05-5 Biphenyl-2,2'-dicarbaldehyde 
• 89-98-5 2-chloro-benzaldehyde 
• 1450806-14-0 C₁₁H₁₀ClF₃O₂ 
• 7237-34-5 2-(hydroxyethyl)triphenylphosphonium bromide 
• 936-51-6 2-phenyl-1,3-dioxolane 
• 1401468-46-9 2-(2-(2-methoxy-2-(2,2,2-trifluoroethoxy)propyl)phenyl)-1,3-dioxoline 
• 96689-74-6 2-(2-propenyl)benzaldehyde ethylene glycol acetal 
• 1394823-21-2 2-(2-(1,3-dioxolan-2-yl)phenyl)-1-phenylpropan-1-one 
• 51089-62-4 4-Methyl-3-phenylisoquinoline 
• 1394824-48-6 4-methyl-3-phenylisoquinoline N-oxide 
• 1122103-26-7 C₁₆H₂₁ClO₃ 
• 1122103-25-6 C₁₄H₁₇ClO₃ 
• 106569-07-7 2,2'-<1,1'-biphenyl>-2,2'-diylbis(1,3-dioxolane) 

Relevant articles and documents

Application of poly(Vinylbenzyltrimethylammonium tribromide) resin as an efficient polymeric catalyst in the acetalization and diacetylation of benzaldehydes

The applications of a new supported tribromide reagent (poly(vinylbenzyltrimethylammonium tribromide) resin) were reported. This supported tribromide resin was used as a catalyst in the acetalization and diacetylation of benzaldehydes under mild conditions with high efficiency. The effects of solvents, and amount of the supported tribromide resin on the reactions were investigated. Under the optimal conditions, most of acetal and 1,1-diacetates of benzaldehydes were selectively obtained in excellent yields.

Design and synthesis of a novel series of cyanoindole derivatives as potent γ-secretase modulators

The discovery, design and synthesis of a new series of GSMs is described. The classical imidazole heterocycle has been replaced by a cyano group attached to an indole nucleus. The exploration of this series has led to compound 26-S which combined high in

New Br?nsted-Lewis acidic quaternary ammonium ionic liquids: Synthesis, acidity determination and acidity-catalytic activity relationship

A series of new Br?nsted-Lewis acidic ionic liquids, which are operational simplicity, high stability, low cost and applicable for scaling up, have been synthesized and their activity for acetalization was examined. The comprehensive studies on the acidity-catalytic performance relationship of the Br?nsted-Lewis acidic ionic liquids were performed. IR spectroscopy results confirmed that the new Br?nsted-Lewis acidic ionic liquids possess both Br?nsted and Lewis acid sites. The acidities were determined by Hammett method, and further studies on acidity-activity relationship revealed that the acidity played a key role in the acid-catalyzed probe reactions.