56180-50-8

Basic information

• Product Name: Cyclohexanone, 4,4-dimethoxy-
• Synonyms: Cyclohexanone, 4,4-dimethoxy-
• CAS NO: 56180-50-8
• Molecular Formula: C₈H₁₄O₃
• Molecular Weight: 158.197
• Mol File: 56180-50-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 212.646 °C at 760 mmHg
• Flash Point: 72.647 °C
• Density: 1.038 g/cm³
• CAS DataBase Reference: Cyclohexanone, 4,4-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 4,4-dimethoxy-(56180-50-8)
• EPA Substance Registry System: Cyclohexanone, 4,4-dimethoxy-(56180-50-8)

Safety Data

• Hazardous Substances Data: 56180-50-8(Hazardous Substances Data)

Usage

General Description

4,4-dimethoxy-Cyclohexanone, also known as 1,3-Dioxolanylcyclohexane, is a chemical compound classified under bicyclic compounds. It features a cyclohexanone, a six-membered cyclic ketone, and two methoxy groups (OCH3) on the same carbon, making it a dialkyl ether. This chemical is colorless and demonstrates a pleasant smell. It is not widely researched or commercially used, so specific applications, toxicity, or health implications are less known or reported. Its molecular formula is C9H16O3 and its stand-alone molar mass is 172.22 g/mol. It is stable, non-volatile, and mostly used in research or experimental work. Lastly, due to its less known toxicity data, it is expected to be handled with general laboratory precautions while in use.

Upstream product

• 112906-44-2 4,4-dimethoxycyclohexanol 
• 67-56-1 methanol 
• 637-88-7 1,4-Cyclohexanedione 
• 150-76-5 4-methoxy-phenol 
• 69125-55-9 4-hydroxy-1-methoxy-1-cyclohexene 
• 935-50-2 4,4-dimethoxycyclohexa-2,5-dienone 

Downstream Products

• 124549-70-8 1,1-dimethoxy-4-hydroxy-4-(2'-piperidyl)cyclohexane 
• 124549-74-2 4-hydroxy-1-methoxy-4-(2'-piperidyl)cyclohex-1-ene 
• 124549-79-7 methoxymethyl ether of 1,1-dimethoxy-4-hydroxy-4-(2'-piperidyl)cyclohexane 
• 124549-78-6 methoxymethyl ether of 1,1-dimethoxy-4-hydroxy-4-(2'-pyridyl)cyclohexane 
• 124568-67-8 1,1-dimethoxy-4-hydroxy-4-(2'-pyridyl)cyclohexane 
• 1403578-37-9 C₂₄H₂₆O₇S₂ 

Relevant articles and documents

Chemoselective Two-Directional Reaction of Bifunctionalized Substrates: Formal Ketal-Selective Mukaiyama Aldol Type Reaction

In the presence of an acidic zwitterion bearing a highly stabilized carbanion, reactions of ω,ω-dialkoxy carbonyl compounds with ketene silyl acetals (KSA) resulted in an unusual molecular transformation; substitution reaction with the KSA at the ketal mo

Method for the Production of Substituted and Unsubstituted Cyclohexanone Monoketals

The invention relates to a novel process for preparing and isolating known substituted and unsubstituted 1,4-cyclohexanone monoketals.

CONJUGATE REDUCTION OF POLYFUNCTIONAL α,β-UNSATURATED CARBONYL COMPOUNDS USING 6. COMPATIBILITY WITH HALOGEN, SULFONATE, AND SULFUR SUBSTITUENTS

In contrast to organocuprate conjugate addition and standard methods for conjugate reduction, use of the stable copper(I) hydride cluster, 6, allows chemoselective conjugate reduction of α,β-unsaturated carbonyl compounds substituted at the γ-position with leaving groups.In addition, the compatibility of the conjugate reduction with organic halides and sulfonate groups is demonstrated.