1607-37-0

Basic information

• Product Name: 4-[(2,3-EPOXYPROPOXY)METHYL]-2,2-DIMETHYL-1,3-DIOXOLANE
• Synonyms: ISOPROPYLIDENGLYCEROLGLYCIDYL ETHER;4-[(2,3-EPOXYPROPOXY)METHYL]-2,2-DIMETHYL-1,3-DIOXOLANE;2,2-diMethyl-4-[(oxiran-2-ylMethoxy)Methyl]-1,3-dioxolane
• CAS NO: 1607-37-0
• Molecular Formula: C9H16O4
• Molecular Weight: 188.22
• Mol File: 1607-37-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 266.474°C at 760 mmHg
• Flash Point: 113.528°C
• Appearance: /
• Density: 1.085g/cm³
• Vapor Pressure: 0.014mmHg at 25°C
• Refractive Index: 1.446
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• CAS DataBase Reference: 4-[(2,3-EPOXYPROPOXY)METHYL]-2,2-DIMETHYL-1,3-DIOXOLANE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[(2,3-EPOXYPROPOXY)METHYL]-2,2-DIMETHYL-1,3-DIOXOLANE(1607-37-0)
• EPA Substance Registry System: 4-[(2,3-EPOXYPROPOXY)METHYL]-2,2-DIMETHYL-1,3-DIOXOLANE(1607-37-0)

Safety Data

• Hazardous Substances Data: 1607-37-0(Hazardous Substances Data)

Usage

General Description

"4-[(2,3-Epoxypropoxy)methyl]-2,2-dimethyl-1,3-dioxolane" is a chemical compound with the molecular formula C9H16O4. It is a colorless liquid with a molecular weight of 188.22 g/mol. 4-[(2,3-EPOXYPROPOXY)METHYL]-2,2-DIMETHYL-1,3-DIOXOLANE is often used as a solvent in various industrial and research applications. It is also used as an intermediate in the synthesis of other organic compounds. The presence of the epoxy and dioxolane functional groups gives this compound unique reactivity and properties, making it useful in a variety of chemical processes. However, it is important to handle and use this compound with caution due to its potential for skin and eye irritation and its flammability.

InChI:InChI=1/C9H16O4/c1-9(2)12-6-8(13-9)4-10-3-7-5-11-7/h7-8H,3-6H2,1-2H3

Upstream product

• 106-89-8 epichlorohydrin 
• 100-79-8 (R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol 

Downstream Products

• 18180-30-8 prop-2-ynyloxymethyl-oxirane 

Relevant articles and documents

Tuning the DNA binding and cleavage of bpa Cu(II) complexes by ether tethers with hydroxyl and methoxy groups

Five bpa (bis(2-picolyl)amine) derivatives (1b, 2e, 3f, 4c, 5d) carrying ether tethers with hydroxyl and methoxy groups, have been synthesized from pyridine aldehyde and the respective amines by reductive amination. Their Cu(II) complexes carrying additio

Multihydroxyl-functional polystyrenes in continuous flow

We describe the synthesisof end-functionalized polystyrenes byliving anionic polymerization ina microstructured reactor via termination by acetal-protected functional epoxides. Initiation of styrene polymerization by alkyllithium takes place in a micromix

Fluorine-containing nitroazole derivatives and radiosensitizer comprising the same

A nitroazole derivative of the formula: wherein NA is 3-nitro-1,2,4-triazol-l-yl and Rf is a fluorine-containing organic group which is useful as a radiosensitizer.