6413-52-1

Basic information

• Product Name: 1,3-Dioxane,2-(4-chlorophenyl)-(9CI)
• Synonyms: 1,3-Dioxane,2-(4-chlorophenyl)-(9CI)
• CAS NO: 6413-52-1
• Molecular Formula: C₁₀H₁₁ClO₂
• Molecular Weight: 198.64614
• Product Categories: PHENYL
• Mol File: 6413-52-1.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 289.8°C at 760 mmHg
• Flash Point: 118.1°C
• Appearance: /
• Density: 1.206g/cm³
• Vapor Pressure: 0.00374mmHg at 25°C
• Refractive Index: 1.531
• CAS DataBase Reference: 1,3-Dioxane,2-(4-chlorophenyl)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxane,2-(4-chlorophenyl)-(9CI)(6413-52-1)
• EPA Substance Registry System: 1,3-Dioxane,2-(4-chlorophenyl)-(9CI)(6413-52-1)

Safety Data

• Hazardous Substances Data: 6413-52-1(Hazardous Substances Data)

Usage

General Description

1,3-Dioxane,2-(4-chlorophenyl)-(9CI) is a chemical compound with the molecular formula C8H9ClO2. It is a chlorinated derivative of 1,3-dioxane and is classified as an organic compound. It is a colorless liquid with a slightly sweet odor, and is used in the production of various products including solvents, pharmaceuticals, and agricultural chemicals. It is also used as an intermediate in the synthesis of other organic compounds. This chemical is considered to be hazardous to human health, with potential adverse effects on the respiratory system, skin, and eyes. It is important to handle this chemical with caution and in accordance with safe handling procedures.

InChI:InChI=1/C10H11ClO2/c11-9-4-2-8(3-5-9)10-12-6-1-7-13-10/h2-5,10H,1,6-7H2

Upstream product

• 504-63-2 trimethyleneglycol 
• 28291-10-3 trans-2-(4-chlorobenzenyl)-3-phenyl-oxirane 
• 104-88-1 4-chlorobenzaldehyde 
• 3395-81-1 4-chlorobenzaldehyde dimethyl acetal 
• 69404-95-1 tert-butyldimethyl(3-phenylpropoxy)silane 
• 22391-05-5 2-(4-chlorophenyl)-1,3-oxathiolane 
• 17887-80-8 1,3-bis(trimethylsiloxy)propane 

Downstream Products

• 81172-92-1 4-(1,3-dioxan-2-yl)benzaldehyde 
• 4750-61-2 N-(p-chlorobenzyl)aniline 
• 1236-90-4 2-(4-chlorophenyl)-4-phenylquinoline 
• 1243701-29-2 C₁₅H₁₉ClO₃ 
• 104-88-1 4-chlorobenzaldehyde 
• 10359-09-8 2-(4-chlorophenyl)-1,3-dithiane 
• 831-81-2 4-chlorophenyl(phenyl)methane 
• 30203-87-3 1-chloro-4-(4-methylbenzyl)benzene 
• 91410-28-5 1-chloro-4-(3-methylbenzyl)benzene 
• 55676-88-5 1-chloro-4-(2-methylbenzyl)benzene 
• 74-11-3 para-chlorobenzoic acid 
• 130534-90-6 4-Chloro-benzoic acid 3-hydroxy-propyl ester 
• 32377-36-9 anilino(4-chlorophenyl)acetonitrile 

Relevant articles and documents

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.

A METHOD OF ACETALIZING AN ALDEHYDE

A method of acetalizing an aldehyde comprising reacting said aldehyde with an alcohol in the presence of a polymeric catalyst to form an acetal wherein the polymeric catalyst is a mesoporous poly-melamine-formaldehyde polymer.