20761-68-6

Basic information

• Product Name: (5-ethyl-2,2-dimethyl-1,3-dioxan-5-yl)methanol
• Synonyms: (5-Ethyl-2,2-dimethyl-1,3-dioxan-5-yl)methanol; 1,3-dioxane-5-methanol, 5-ethyl-2,2-dimethyl-
• CAS NO: 20761-68-6
• Molecular Formula: C₉H₁₈O₃
• Molecular Weight: 174.2374
• Mol File: 20761-68-6.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 232.7°C at 760 mmHg
• Flash Point: 110.5°C
• Density: 0.959g/cm³
• Vapor Pressure: 0.0108mmHg at 25°C
• Refractive Index: 1.425
• CAS DataBase Reference: (5-ethyl-2,2-dimethyl-1,3-dioxan-5-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (5-ethyl-2,2-dimethyl-1,3-dioxan-5-yl)methanol(20761-68-6)
• EPA Substance Registry System: (5-ethyl-2,2-dimethyl-1,3-dioxan-5-yl)methanol(20761-68-6)

Safety Data

• Hazardous Substances Data: 20761-68-6(Hazardous Substances Data)

Usage

General Description

(5-ethyl-2,2-dimethyl-1,3-dioxan-5-yl)methanol is a chemical compound that belongs to the class of alcohols. It is derived from the dioxane family, which consists of a six-membered carbon ring with two oxygen atoms. The presence of the ethyl and dimethyl groups in the compound suggests that it may have some solvent properties. The hydroxyl group indicates that it is capable of forming hydrogen bonds with other molecules, which could make it useful in various chemical and biological processes. Overall, (5-ethyl-2,2-dimethyl-1,3-dioxan-5-yl)methanol is a versatile compound with potential applications in industries such as pharmaceuticals, cosmetics, and chemical synthesis.

Upstream product

• 77-99-6 1,1,1-tri(hydroxymethyl)propane 
• 104-15-4 toluene-4-sulfonic acid 
• 77-76-9 2,2-dimethoxy-propane 
• 534-15-6 1,1-dimethoxyethane 
• 6192-52-5 p-toluenesulfonic acid monohydrate 
• 444816-10-8 triethyl-(5-ethyl-2,2-dimethyl-[1,3]dioxan-5-ylmethoxy)-silane 
• 67-64-1 acetone 

Downstream Products

• 34541-83-8 toluene-4-sulfonic acid 5-ethyl-2,2-dimethyl-[1,3]dioxan-5-ylmethyl ester 
• 682-11-1 trimethylol propane monoallyl ether 
• 174141-08-3 5-ethyl-5-{[(p-vinylphenyl)methoxy]methyl}-1,3-dioxan-2-one 
• 162461-18-9 2-ethyl-2-{[(p-vinylphenyl)methoxy]methyl}-1,3-propanediol 

Relevant articles and documents

Synthesis of high molecular flexibility polycarbonates for solid polymer electrolytes

A new self-plasticizing aliphatic polycarbonate comprising flexible alkyl and alkyl ether side groups was designed and synthesized from six-membered cyclic carbonate monomers with the aim of producing a material with high molecular flexibility (low Tg) and concomitant high ionic conductivity when used as a polymer electrolyte. The Tg of the novel polycarbonate was determined to be -49.4 °C at a molecular weight of 34 400 g mol-1, which is the lowest reported Tg to date for a substituted poly(trimethylene carbonate). UV-crosslinked polymer electrolytes were produced based on this novel material together with LiTFSI salt and showed ionic conductivities in the range of 2 × 10-8 to 2 × 10-7 S cm-1 at room temperature and 1 × 10-6 to 1 × 10-5 S cm-1 at 100 °C. The limited ionic conductivities of these electrolytes indicate that high molecular flexibility alone does not guarantee fast ion transport in solid polymer electrolytes and that other factors, such as the polarity of the polymer host material, will also influence the transport properties of the electrolyte.

Reversible switching between linear and ring polystyrenes bearing porphyrin end groups

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SALT, ACID GENERATOR, RESIST COMPOSITION, AND METHOD FOR PRODUCING RESIST PATTERN

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