5406-38-2

Usage

Explanation

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

Explanation

It is a derivative of dioxane, which means it is structurally related to dioxane but has undergone a chemical modification.

Explanation

The compound contains a chlorine atom that is part of a phenyl ring, which is a six-carbon ring with alternating single and double bonds.

Explanation

It is used as an intermediate in the production of various pharmaceuticals, pesticides, and other organic chemicals due to its chemical reactivity.

Explanation

It is used as a solvent in various industrial processes, taking advantage of its ability to dissolve other substances.

Explanation

Studies have shown that 1,3-Dioxane, 2-(2-chlorophenyl)-(9CI) may have carcinogenic properties, meaning it could potentially cause cancer.

Explanation

The compound has been found to have toxic effects on human health and the environment, which is why its use and disposal should be carefully managed.

Explanation

Proper handling, storage, and disposal methods are essential to minimize the risks associated with the compound's potential carcinogenic and toxic effects.

Derivative of Dioxane

Yes

Chlorine Atom

Attached to a phenyl ring

Common Uses

Pharmaceutical synthesis, pesticide synthesis, and other organic chemicals

Industrial Application

Solvent

Potential Carcinogenic Effects

Yes

Toxic Effects

Yes

Environmental and Health Risks

High

Disposal and Management

Careful handling required

InChI:InChI=1/C10H11ClO2/c11-9-5-2-1-4-8(9)10-12-6-3-7-13-10/h1-2,4-5,10H,3,6-7H2

Upstream product

• 89-98-5 2-chloro-benzaldehyde 
• 504-63-2 trimethyleneglycol 
• 70380-66-4 2-chlorobenzaldehyde dimethyl acetal 

Downstream Products

• 89-98-5 2-chloro-benzaldehyde 
• 69849-09-8 2-(2-chlorophenyl)-1,3-dithiane 

Relevant academic research and scientific papers

Practical acetalization and transacetalization of carbonyl compounds catalyzed by recyclable PVP-I

A novel PVP-I catalyzed acetalizations/transacetalizations of carbonyl compounds has been developed processing with a mild and easy handling fashion. Different types of Acyclic and cyclic acetals were prepared from carbonyl compounds or their acetals successfully. Further applications of newly developed catalytic combination were testified. This protocol featured with simplicity of operation, mild reaction condition, short reaction time, recyclable of catalyst and broad substrates scope with excellent yields.

House bulb light-induced photochemical acetalization of carbonyl compounds catalyzed by Eosin Y

We have systematically studied the reactions of acetalization and found that high reaction efficiency can be achieved using cheap and readily available organic Eosin Y as catalyst. The reaction proceeds smoothly under house bulbs and shows excellent functional group tolerance. The substrates of the reaction system are compatible with aromatic aldehydes, aliphatic aldehydes, aromatic ketones, and cyclic ketones with high yields.

Acetalization of carbonyl compounds catalyzed by bismuth triflate under solvent-free conditions

Carbonyl compounds were converted to the corresponding 1,3-dioxolanes and 1,3-dioxanes with ethylene glycol and 1,3-propandiol in the presence of bismuth triflate under solvent-free conditions. In addition, high chemoselective protection of aldehydes in the presence of ketones has been achieved.

Highly efficient and chemoselective acetalization of carbonyl compounds catalyzed by new and reusab e zirconyl triflate, zr0(0tf)2

Various types of aromatic aldehydes were efficiently converted to their corresponding 1,3-dioxanes and 1,3-dioxolane with 1,3-propanediol and ethylene glycol, respectively, in the presence of catalytic amount of ZrO(OTf) 2 in acetonitrile at room temperature. The catalyst can be reused several times without loss of its catalytic activity. Very short reaction times, selective acetalization of aromatic aldehydes in the presence of aliphatic aldehydes and ketones, very mild reaction conditions, reusability of the catalyst, and easy workup are noteworthy advantages of this method.

2,4,4,6-Tetrabromo-2,5-cyclohexadienone (TABCO) as a versatile, efficient, and chemoselective catalyst for the acetalization and transacetalization of carbonyl compounds, the preparation of acetonides from epoxides and acylals (1,1-diacetates) from aldehydes

The efficient and chemoselective preparation of acetals and ketals from carbonyl compounds, transacetalization reactions, the conversion of epoxides to acetonides, and the preparation of acylals from aldehydes in the presence of catalytic amounts of 2,4,4,6-tetrabromo-2,5-cyclohexadienone (TABCO) are described.