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N-(11-Bromoundecyl)carbamic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

463930-53-2

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463930-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 463930-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,3,9,3 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 463930-53:
(8*4)+(7*6)+(6*3)+(5*9)+(4*3)+(3*0)+(2*5)+(1*3)=162
162 % 10 = 2
So 463930-53-2 is a valid CAS Registry Number.

463930-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-propanyl (11-bromoundecyl)carbamate

1.2 Other means of identification

Product number -
Other names t-butyl 11-bromoundecanoate

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:463930-53-2 SDS

463930-53-2Relevant academic research and scientific papers

Synthesis of bifunctional hydroxamic acids as novel ligands for the hydrophilic stabilization of iron oxide nanoparticles

Hofmann, Andreas,Graf, Christina,Kung, Shih-Hao,Kim, Myeongseob,Peng, Xiaogang,El-Aama, Randa,Ruehl, Eckart

experimental part, p. 1150 - 1158 (2010/06/13)

A general method for synthesizing bifunctional hydroxamic acids containing carboxylic acid or amino functionalities is reported. Various products from simple alkyl to complex dendrimer-like structures are described. Such molecules have recently been used in ligand-exchange reactions for the hydrophilic stabilization of originally oleic acid protected iron oxide nanoparticles. Georg Thieme Verlag Stuttgart · New York.

Inkless microcontact printing on self-assembled monolayers of Fmoc-protected aminothiols

Shestopalov, Alexander A.,Clark, Robert L.,Toone, Eric J.

, p. 13818 - 13819 (2008/03/30)

Here we describe a new microcontact printing technique (μCP), based on a catalytic reaction between an Fmoc-protected self-assembled monolayer (SAM) of aminothiols chemisorbed on a gold surface and an elastomeric stamp bearing covalently attached piperidine. The elastomeric stamp was used to selectively cleave Fmoc groups from the surface of a SAM on gold in the places of conformal contact. The technique permits nanoscale pattern fabrication with edge resolution less than 50 nm, avoiding problems of conventional microcontact printing associated with diffusion of chemical ink , and provides a simple method for the chemical modification of SAMs. Copyright

Immobilization of rhodium complexes at thiolate monolayers on gold surfaces: Catalytic and structural studies

Belser, Thomas,Stoehr, Meike,Pfaltz, Andreas

, p. 8720 - 8731 (2007/10/03)

Chiral rhodium-diphosphine complexes have been incorporated into self-assembled thiolate monolayers (SAMs) on gold colloids. Catalysts of this type are of interest because they combine properties of homogeneous and heterogeneous systems. In addition, it s

Alkylamine derivates as anti-fouling agents

-

, (2008/06/13)

The invention relates to new and known compounds as well as methods for preventing the attachment of aquatic organisms to surfaces which are submerged for extensive periods of time in water. More particularly, this invention relates to the protection of submerged surfaces with new alkylamine derivatives as antifouling agents. The invention is beneficiary for the environment in that it will permit the use of copper- and tin-free paints.

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