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Piperidine, 1-[1-[4-(chloromethyl)phenyl]ethoxy]-2,2,6,6-tetramethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

212132-38-2

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212132-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 212132-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,1,3 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 212132-38:
(8*2)+(7*1)+(6*2)+(5*1)+(4*3)+(3*2)+(2*3)+(1*8)=72
72 % 10 = 2
So 212132-38-2 is a valid CAS Registry Number.

212132-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-{1-[4-(Chloromethyl)phenyl]ethoxy}-2,2,6,6-tetramethylpiperidin e

1.2 Other means of identification

Product number -
Other names 1H-Pyrrole,1-[[4-(chloromethyl)phenyl]methyl]

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:212132-38-2 SDS

212132-38-2Downstream Products

212132-38-2Relevant academic research and scientific papers

Effects of dendron generation and salt concentration on phase structures of dendritic-linear block copolymers with a semirigid dendron containing PEG tails

Cai, Huanhuan,Jiang, Guoliang,Shen, Zhihao,Fan, Xinghe

experimental part, p. 6176 - 6184 (2012/10/18)

We prepared a series of dendritic-linear block copolymers (DLBCPs) bearing a semirigid Percec-type dendron with ionophilic poly(ethylene glycol) (PEG) tails and a polystyrene (PS) linear polymer by nitroxide-mediated living radical polymerization (NMRP).

Multi-armed, TEMPO-functionalized unimolecular initiators for starburst dendrimer synthesis via stable free radical polymerisation. 2. Tris (1,3,5)benzyloxy unimers

Ghani, Mohmad Asri Abd,Abdallah, Dalia,Kazmaier, Peter M.,Keoshkerian, Barkev,Buncel, Erwin

, p. 1403 - 1412 (2007/10/03)

The synthesis of the trifunctionalized TEMPO-modified unimolecular initiators, unimers I, II, and III is described. Unimer I was prepared via an SN2 type Williamson ether coupling of 1,3,5-tris(iodomethyl)benzene with a TEMPO-containing ethylbenzene hydroxy derivative. The synthesis of unimer II, however, was accomplished through SN1 reaction of 1,3,5-tris(bromomethyl)benzene with the hydroxy-ethylbenzene TEMPO derivative in the presence of silver triflate. Synthesis of unimer III started from phloroglucinol and an SNAr reaction with 1-fluoro-4-nitrobenzene, followed by reduction to the amino compound and Schiff base formation with the TEMPO-derivatized aromatic aldehyde. Stable free radical polymerisation (SFRP) of styrene and acetoxystyrene with unimer I are also described with molecular weights and polydispersities reported. It is concluded that the SFRP of styrene with a triradical initiator meets the requirements of a living system.

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