23510-92-1

Basic information

• Product Name: 4β-Ethoxycyclohexanone
• Synonyms: 4-Ethoxycyclohexanone;4β-Ethoxycyclohexanone;1-Ethoxy-4-oxocyclohexane;4-Ethoxycyclohexan-1-one 97%;4-Ethoxycyclohexan-1-one97%;4-ethoxycyclohexan-1-one
• CAS NO: 23510-92-1
• Molecular Formula: C₈H₁₄O₂
• Molecular Weight: 142.2
• Mol File: 23510-92-1.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 88-90 °C(Press: 12 Torr)
• Appearance: /
• Density: 0.97±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4β-Ethoxycyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: 4β-Ethoxycyclohexanone(23510-92-1)
• EPA Substance Registry System: 4β-Ethoxycyclohexanone(23510-92-1)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 23510-92-1(Hazardous Substances Data)

Usage

General Description

4β-Ethoxycyclohexanone is a chemical compound with the molecular formula C9H16O2. It is a cyclic ketone with an ethoxy group attached to the beta carbon of the cyclohexane ring. 4β-Ethoxycyclohexanone is commonly used as a building block in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. It is also used as a flavoring agent and fragrance in the food and cosmetic industries. 4β-Ethoxycyclohexanone is a colorless liquid with a sweet, fruity odor and is considered to be relatively stable under normal conditions. It should be handled and stored with care, as it may be harmful if ingested or inhaled, and can cause irritation to the skin and eyes upon contact.

Upstream product

• 106349-63-7 4-ethoxycyclohexan-1-ol 
• 22428-87-1 4,4-ethylenedioxycyclohexan-1-ol 
• 75-03-6 ethyl iodide 
• 55103-52-1 4-ethoxycyclohexanone ethylene ketal 
• 4746-97-8 cyclohexanedione monoethylene ketal 
• 637-88-7 1,4-Cyclohexanedione 
• 622-62-8 4-Ethoxyphenol 
• 556-48-9 1,4-Cyclohexanediol 

Downstream Products

• 90722-88-6 4-Ethoxy-1-trichlormethyl-cyclohexanol-⁽¹⁾ 
• 192504-15-7 4-Ethoxycyclohexanon-2,2,6,6-d⁽⁴⁾ 
• 106349-63-7 4-ethoxycyclohexan-1-ol 
• 192504-16-8 C₈H₁₅⁽²⁾HO₂ 
• 1315073-06-3 4-2-[2-(2-methoxyethoxy)ethoxy]ethoxycyclohexanone 

Relevant articles and documents

IRAK INHIBITORS AND METHOD FOR MAKING AND USING

Disclosed embodiments concern interleukin receptor associated kinases (IRAK) inhibitors, such as oxazole compounds, and compositions comprising such inhibitors. Also disclosed are methods of making and using the compounds and compositions. The disclosed c

Thermoresponsive star-like γ-substituted poly(caprolactone)s for micellar drug delivery

Temperature responsive drug carriers are attractive due to their ability to provide controlled release of the encapsulated cargo based on the use of external stimuli. In this work, 4- and 6-arm thermoresponsive star-like block copolymers were synthesized

A combined experimental and computational study of the substituent effect on micellar behavior of γ-substituted thermoresponsive amphiphilic poly(ε-caprolactone)s

The effect of the core substituent structure on the micellar behavior of thermoresponsive amphiphilic poly(ε-caprolactone) diblock copolymer micelles was investigated through a combination of experimental and computational methods. The polycaprolactone (P