3066-70-4

Basic information

• Product Name: 2,3-DIBROMOPROPYL METHACRYLATE
• Synonyms: 2,3-DIBROMOPROPYL METHACRYLATE;methacrylicacid,2,3-dibromopropylester;2,3-dibromopropyl 2-methylprop-2-enoate;2-methylacrylic acid 2,3-dibromopropyl ester
• CAS NO: 3066-70-4
• Molecular Formula: C7H10Br2O2
• Molecular Weight: 285.96
• Product Categories: monomer
• Mol File: 3066-70-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 291.8°Cat760mmHg
• Flash Point: 130.3°C
• Appearance: /
• Density: 1.69g/cm³
• Vapor Pressure: 0.0019mmHg at 25°C
• Refractive Index: 1.517
• CAS DataBase Reference: 2,3-DIBROMOPROPYL METHACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DIBROMOPROPYL METHACRYLATE(3066-70-4)
• EPA Substance Registry System: 2,3-DIBROMOPROPYL METHACRYLATE(3066-70-4)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 3066-70-4(Hazardous Substances Data)

Usage

General Description

Clear brown liquid.

Air & Water Reactions

Highly flammable. Insoluble in water.

Health Hazard

ACUTE/CHRONIC HAZARDS: 2,3-DIBROMOPROPYL METHACRYLATE has toxic and hazardous decomposition products. It is probably an irritant.

Fire Hazard

2,3-DIBROMOPROPYL METHACRYLATE is considered to be combustible.

InChI:InChI=1/C7H10Br2O2/c1-5(2)7(10)11-4-6(9)3-8/h6H,1,3-4H2,2H3

Upstream product

• 96-13-9 2,3-Dibromopropan-1-ol 
• 920-46-7 Methacryloyl chloride 
• 106-91-2 2,3-Epoxypropyl methacrylate 

Relevant articles and documents

POLYMERIZABLE COMPOUNDS WITH ONE OR MORE SURFACTANT-LIKE PROPERTIES

Some embodiments of the present disclosure relate to polymerizable compounds that comprise biocidal activity and/or the potential for increased biocidal activity and that comprise at least one hydrophobic portion and at least one hydrophilic portion. Together the hydrophobic portion and the hydrophilic portion of the compounds may provide the polymerizable compounds with one or more surfactant-like properties. The polymerizable compounds can be incorporated into polymer coating formulations. The polymer coating formulations can be used to coat one or more surfaces of a substrate. The coating formulation can provide biocidal activity and/or the potential for increased biocidal activity to the coated substrate-surface.

Regioselective synthesis of vic-halo alcohols and symmetrical or unsymmetrical vic-dihalides from epoxides using triphenylphosphine -N-halo imides

A simple, novel, and highly regioselective cleavage of epoxides into vicinal halo alcohols and symmetrical or unsymmetrical dihalides is described using different stoichiometries of triphenylphosphine (PPh3) and N-halo succinimide (NXS) or N-halo saccharine (NXSac).