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2-Propenoic acid, 2-(2-bromo-2-methyl-1-oxopropoxy)ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

213453-02-2

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213453-02-2 Usage

Chemical compound

2-Propenoic acid, 2-(2-bromo-2-methyl-1-oxopropoxy)ethyl ester

Main properties

Used in production of polymers, adhesives, and coatings
Clear liquid with sharp, pungent odor
Highly reactive with strong oxidizing agents
Monomer in synthesis of various polymers
Ability to crosslink and create strong, durable bonds
Can cause skin and eye irritation
Should be handled with care
Should be stored in cool, well-ventilated area away from direct sunlight and heat sources

Check Digit Verification of cas no

The CAS Registry Mumber 213453-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,4,5 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 213453-02:
(8*2)+(7*1)+(6*3)+(5*4)+(4*5)+(3*3)+(2*0)+(1*2)=92
92 % 10 = 2
So 213453-02-2 is a valid CAS Registry Number.

213453-02-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-prop-2-enoyloxyethyl 2-bromo-2-methylpropanoate

1.2 Other means of identification

Product number -
Other names 2-acryloyloxyethyl 2-bromoisobutyrate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:213453-02-2 SDS

213453-02-2Downstream Products

213453-02-2Relevant academic research and scientific papers

Inimer graft-copolymerized poly(vinylidene fluoride) for the preparation of arborescent copolymers and surface-active copolymer membranes

Zhai, Guangqun,Kang,Neoh

, p. 7240 - 7249 (2007/10/03)

A novel graft copolymer was synthesized via graft copolymerization of an inimer, 2-(2-bromoisobutyryloxy)ethyl acrylate (BIEA), with ozone-pretreated poly(vinylidene fluoride) (PVDF) (the PVDF-g-PBIEA copolymer). Porous membranes could be fabricated from the copolymer solution by phase inversion. The BIEA polymer (PBIEA) side chains allowed the initiation of atom transfer radical polymerization (ATRP) of functional monomers on the copolymer and the membrane surface. An arborescent copolymer was prepared via ATRP of sodium 4-styrenesulfonate (NaSS) initiated from the PVDF-g-PBIEA copolymer side chains (PVDF-g-PBIEA-ar-NaPSS copolymer). In comparison with the PVDF-g-PBIEA-ar-NaPSS copolymer membrane cast in water by phase inversion, the copolymer membrane cast in 1 M aqueous NaCl solution had enriched NaPSS side chains on the surface and larger pore size. The PVDF-g-PBIEA-ar-PPEGMA membrane was prepared via the surface-initiated ATRP of poly(ethylene glycol) methacrylate (PEGMA) on the porous PVDF-g-PBIEA membrane. Protein adsorption studies indicated that the PVDF-g-PBIEA-ar-PPEGMA membrane exhibited substantially improved antifouling properties. Thus, the PVDF-g-PBIEA membranes with the active ATRP inimer repeat units on the surface offers opportunities for the functionalization of membranes via surface molecular design.

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