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495417-67-9

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495417-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 495417-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,5,4,1 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 495417-67:
(8*4)+(7*9)+(6*5)+(5*4)+(4*1)+(3*7)+(2*6)+(1*7)=189
189 % 10 = 9
So 495417-67-9 is a valid CAS Registry Number.

495417-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[(tert-butyldimethylsilyl)oxy]ethoxy]ethyl methacrylate

1.2 Other means of identification

Product number -
Other names 2-Methyl-acrylic acid 2-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-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:495417-67-9 SDS

495417-67-9Downstream Products

495417-67-9Relevant articles and documents

Synthesis of water-soluble polymethacrylates by living anionic polymerization of trialkylsilyl-protected oligo(ethylene glycol) methacrylates

Ishizone, Takashi,Han, Seok,Okuyama, Syunsuke,Nakahama, Seiichi

, p. 42 - 49 (2007/10/03)

2-[2-[(tert-Butyldimethylsilyl)oxy]ethoxy]ethyl methacrylate (2) and 2-[2-[2-[(tert-butyldimethylsilyl)oxy] ethoxy] ethoxy] ethyl methacrylate (3) were polymerized anionically in THF at -78 °C for 2-24 h. The anionic initiator systems included 1,1-diphenyl-3-methylpentyllithium/lithium chloride and diphenylmethylpotassium/diethylzinc. The polymerization of novel tert-butyldimethylsilyl-protected oligo(ethylene glycol) methacrylates, 2 and 3, proceeded quantitatively in each case. The resulting polymers possessed the predicted molecular weights based on the molar ratios of monomers to initiators, and narrow molecular weight distributions (Mw/Mn 1.1). The stability of the propagating carbanion of poly(2) and poly(3) was ascertained by the quantitative efficiencies of the sequential block copolymerizations using tert-butyl methacrylate (tBMA). Well-defined block copolymers, poly(2)-block-poly(tBMA) and poly(3)block-poly(tBMA), were obtained. The trialkylsilyl protecting groups of poly(2) and poly(3) were quantitatively hydrolyzed using 2 N HC1 in aqueous THF at 0 °C for 2 h to give tailored poly[di(ethylene glycol) methacrylate] and poly[tri(ethylene glycol) methacrylate], respectively. Both polymethacrylates obtained after deprotection were readily soluble in water due to the high polarity of the hydrophilic oligo(ethylene glycol) pendant units with terminal OH functionality.

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