13410-58-7

Basic information

• Product Name: 2,2'-((1-Methylethylidene)bis(cyclohexane-4,1-diyloxymethylene))bisoxirane
• Synonyms: Oxirane,2,2'-[(1-methylethylidene)bis(4,1-cyclohexanediyloxymethylene)]bis-;Bisphenol A diglycidyl ether, hydrogenated;2,2'-[(Dimethylmethylene)bis(cyclohexane-4,1-diyloxymethylene)]bisoxirane;2,2'-[Dimethylmethylenebis[(1,4-cyclohexanediyloxy)methylene]]bisoxirane;2,2'-[Isopropylidenebis[(cyclohexane-4,1-diyl)(oxy)(methylene)]]di(oxirane);2,2-Bis[4-(glycidyloxy)cyclohexyl]propane;YL-6663;2,2'-[(1-methylethylidene)bis(cyclohexane-4,1-diyloxymethylene)]bisoxirane
• CAS NO: 13410-58-7
• Molecular Formula: C₂₁H₃₆O₄
• Molecular Weight: 352.51
• EINECS: 236-502-3
• Mol File: 13410-58-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 465.1 °C at 760 mmHg
• Flash Point: 119.2 °C
• Appearance: /
• Density: 1.07 g/cm³
• Vapor Pressure: 0Pa at 25℃
• Water Solubility: 63.1mg/L at 20℃
• CAS DataBase Reference: 2,2'-((1-Methylethylidene)bis(cyclohexane-4,1-diyloxymethylene))bisoxirane(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-((1-Methylethylidene)bis(cyclohexane-4,1-diyloxymethylene))bisoxirane(13410-58-7)
• EPA Substance Registry System: 2,2'-((1-Methylethylidene)bis(cyclohexane-4,1-diyloxymethylene))bisoxirane(13410-58-7)

Safety Data

• Hazardous Substances Data: 13410-58-7(Hazardous Substances Data)

Usage

Flammability and Explosibility

Notclassified

Upstream product

• 7783-47-3 tin (II) fluoride 
• 13804-54-1 4,4'-isopropylidenedicyclohexanol 
• 106-89-8 epichlorohydrin 
• 1675-54-3 diphenylolpropane diglycidyl ether 

Downstream Products

• 82810-36-4 C₂₇H₄₄O₈ 

Relevant articles and documents

Selective hydrogenation of aromatic compounds containing epoxy group over Rh/graphite

Catalytic hydrogenation of aromatic compounds containing epoxy group to alicylic compounds has been investigated. Rh supported on graphite with high surface area exhibited superior performance to other supported catalysts for the selective reduction of the aromatic group while retaining epoxy group.

Process for the preparation of glycidyl ethers

An improved process for the preparation of glycidyl ethers of formula I STR1 wherein Q is an aliphatic, cycloaliphatic or araliphatic radical of a valency m, R is --H or --CH3, and m is an integer from 1 to 10, by reacting an alcohol of formula Q--(OH)m with m mol of an epihalohydrin of formula II STR2 in the presence of a catalyst to the corresponding halohydrin ether, and dehydrohalogenating said halohydrin ether with an alkali metal hydroxide to give a compound of formula I, wherein Q, m and R are as defined above and Hal is halogen, which process comprises using as catalyst a) tin difluoride or b) a divalent tin halide in conjunction with a co-catalyst.