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21282-96-2

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21282-96-2 Usage

Safety Profile

Poison by skin contact. Moderatelytoxic by ingestion. A skin and eye irritant. When heated to decomposition it emits acrid smoke andirritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 21282-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,8 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21282-96:
(7*2)+(6*1)+(5*2)+(4*8)+(3*2)+(2*9)+(1*6)=92
92 % 10 = 2
So 21282-96-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O5/c1-3-8(11)13-4-5-14-9(12)6-7(2)10/h3H,1,4-6H2,2H3

21282-96-2SDS

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 3-oxobutanoate

1.2 Other means of identification

Product number -
Other names Butanoic acid,3-oxo-,2-[(1-oxo-2-propen-1-yl)oxy]ethyl ester

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:21282-96-2 SDS

21282-96-2Downstream Products

21282-96-2Relevant articles and documents

Synthesis of phosphorescent iridium-containing acrylic monomers and their room-temperature polymerization by Cu(0)-RDRP

Christopherson, Cheyenne J.,Hackett, Zo? S.,Sauvé, Ethan R.,Paisley, Nathan R.,Tonge, Christopher M.,Mayder, Don M.,Hudson, Zachary M.

, p. 2539 - 2546 (2018)

A series of acrylic monomers based on cyclometalated iridium(III) complexes have been synthesized based on common phosphorescent emitters for organic light-emitting diodes. A simple room-temperature polymerization procedure for these materials was developed using Cu(0) reversible deactivation radical polymerization, providing polymers with low dispersities of 1.08–1.14 at conversions from 81 to 93% when the Ir complexes are copolymerized with a carbazole-based acrylic host. These methods were also found to be suitable for the preparation of high-molecular-weight polymers with Mn approaching 40,000 Da, as well as block copolymers formed in one pot from the chain extension of methyl acrylate. This scalable room-temperature synthesis of iridium-containing copolymers and block copolymers provides a useful route to optoelectronic materials, which we anticipate can be readily adapted to a broad range of acrylic metallopolymers.

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