38252-14-1

Basic information

• Product Name: 5,5-dimethyl-2-(4-methylphenyl)-1,3-dioxane
• Synonyms: 5,5-dimethyl-2-(4-methylphenyl)-1,3-dioxane;1,3-Dioxane,5,5-dimethyl-2-(4-methylphenyl)-(9CI)
• CAS NO: 38252-14-1
• Molecular Formula: C₁₃H₁₈O₂
• Molecular Weight: 0
• Product Categories: PHENYL
• Mol File: 38252-14-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 291°Cat760mmHg
• Flash Point: 137.3°C
• Appearance: /
• Density: 0.994g/cm³
• Vapor Pressure: 0.00349mmHg at 25°C
• Refractive Index: 1.492
• CAS DataBase Reference: 5,5-dimethyl-2-(4-methylphenyl)-1,3-dioxane(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5-dimethyl-2-(4-methylphenyl)-1,3-dioxane(38252-14-1)
• EPA Substance Registry System: 5,5-dimethyl-2-(4-methylphenyl)-1,3-dioxane(38252-14-1)

Safety Data

• Hazardous Substances Data: 38252-14-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H18O2/c1-10-4-6-11(7-5-10)12-14-8-13(2,3)9-15-12/h4-7,12H,8-9H2,1-3H3

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 

Downstream Products

• 1243701-36-1 C₁₈H₂₆O₃ 
• 104-87-0 4-methyl-benzaldehyde 
• 340819-78-5 C₂₈H₃₈O 
• 819077-27-5 4-(2-(4-dodecyloxyphenyl)-(E)-1-ethenyl)-1-benzaldehyde 
• 370104-67-9 1,2,3-Tris-dodecyloxy-5-[(E)-2-(4-vinyl-phenyl)-vinyl]-benzene 
• 253598-62-8 (E)-4-[2-(3,4,5-tridodecyloxyphenyl)ethenyl]benzaldehyde 
• 370104-66-8 5,5-Dimethyl-2-{4-[(E)-2-(3,4,5-tris-dodecyloxy-phenyl)-vinyl]-phenyl}-[1,3]dioxane 
• 340819-77-4 2-{4-[(E)-2-(4-Dodecyloxy-phenyl)-vinyl]-phenyl}-5,5-dimethyl-[1,3]dioxane 
• 38216-94-3 3-(p-Methyl-benzyloxy)-2,2-dimethyl-propanal-⁽¹⁾ 

Relevant articles and documents

Synthesis of novel solid acidic ionic liquid polymer and its catalytic activities

The novel solid acidic ionic liquid polymer has been synthesized through the copolymerization of acidic ionic liquid oligomers and resorcinol- formaldehyde (RF resin). The catalytic activities were investigated through the acetalization. The results showed that the PIL was very efficient for the reactions with the average yield over 99.0%. The procedure was quite simple with just one-step to complete both the reactions. The high hydrophobic BET surface, high catalytic activities and high stability gave the PIL great potential for green chemical processes. Pleiades Publishing, Ltd., 2013.

Bismuth compounds in organic synthesis: Synthesis of dioxanes, dioxepines, and dioxolanes catalyzed by bismuth(III) triflate

A simple method for the synthesis of 1,3-dioxolanes from carbonyl compounds has been developed using 1,2-bis(trimethylsilyloxy)ethane in the presence of bismuth(III) triflate as a catalyst. The bismuth(III) triflate catalyzed synthesis of a range of dioxanes and dioxepines has also been developed. In these latter cases, the carbonyl compound is treated with a diol, and triethyl orthoformate is used as a water scavenger. All these methods avoid the use of a Dean-Stark trap. Georg Thieme Verlag Stuttgart.

Calix[4]oligophenylenevinylene: A new rigid core for the design of π-conjugated liquid crystalline derivatives

The synthesis and the liquid crystalline properties of a new class of conjugated derivatives that assembled four oligophenylenevinylene (OPV) moieties arising from a calix[4]arene core are described. Photophysical investigations also revealed strong elect