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402828-41-5

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402828-41-5 Usage

Uses

Atom transfer Radical Polymerisation (ATRP) initiator commonly used to functionalize noble metal surfaces, and in the preparation of polymer brushes and biodegradable hydrogels. Also may be used to introduce a temperature and light sensitive cleavable region into the polymer.

Check Digit Verification of cas no

The CAS Registry Mumber 402828-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,8,2 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 402828-41:
(8*4)+(7*0)+(6*2)+(5*8)+(4*2)+(3*8)+(2*4)+(1*1)=125
125 % 10 = 5
So 402828-41-5 is a valid CAS Registry Number.

402828-41-5 Well-known Company Product Price

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  • Aldrich

  • (733350)  Bis[2-(2-bromoisobutyryloxy)undecyl]disulfide  97%

  • 402828-41-5

  • 733350-500MG

  • 1,891.89CNY

  • Detail

402828-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-[11-(2-bromo-2-methylpropanoyl)oxyundecyldisulfanyl]undecyl 2-bromo-2-methylpropanoate

1.2 Other means of identification

Product number -
Other names 2'-ETHYL-2,2,2-TRIFLUOROACETOPHENONE

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:402828-41-5 SDS

402828-41-5Relevant articles and documents

Directing self-assembly of nanoparticles at water/oil interfaces

Duan, Hongwei,Wang, Dayang,Kurth, Dirk G.,Moehwald, Helmuth

, p. 5639 - 5642 (2004)

Finding the right angle: The contact angle of nanoparticles at the water/oil interface can be engineered close to 90° by capping with ligands containing carboxylic ester terminal groups. This drives the nanoparticles to self-assemble into close-packed films (see picture), and thus provides the opportunity to create two- or three-dimensional homo- or heterogeneous nanostructures for electronic, optoelectrical, and magnetic applications.

Efficient two-step synthesis of 11,11′-dithiobis[1-(2-bromo-2- methylpropionyloxy)undecane], a conventional initiator for grafting polymer brushes from gold surfaces via ATRP

Belegrinou, Serena,Malinova, Violeta,Masciadri, Raffaello,Meier, Wolfgang

experimental part, p. 3000 - 3007 (2010/11/05)

11,11′-Dithiobis[1-(2-bromo-2-methylpropionyloxy)undecane], a conventional initiator for grafting polymers from gold surfaces, was synthesized in two steps from 11-mercapto-1-undecanol in 88-92% overall yield. Oxidative dimerization of 11-mercapto-1-undecanol with a catalytic amount of sodium iodide and 30% hydrogen peroxide in ethyl acetate proceeded in 96% yield. Esterification with 2-bromoisobutyryl bromide in dichloromethane was clean and almost quantitative (92% yield) with pyridine used as base, whereas triethylamine gave a messy reaction (64% yield). Alternatively, esterification with 2-bromo-2-methyl-propanoic acid in dichloromethane occurred readily under Steglich′s conditions with N,N′-dicyclohexylcarbodiimide (DCC) and a catalytic amount of dimethylaminopyridine (DMAP; 88% yield). Copyright Taylor & Francis Group, LLC.

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