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108481-83-0

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108481-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108481-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,4,8 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 108481-83:
(8*1)+(7*0)+(6*8)+(5*4)+(4*8)+(3*1)+(2*8)+(1*3)=130
130 % 10 = 0
So 108481-83-0 is a valid CAS Registry Number.

108481-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxy-benzyl)-trimethyl-ammonium, bromide

1.2 Other means of identification

Product number -
Other names .Trimethyl-(4-methoxy-benzyl)-ammoniumhydroxid

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:108481-83-0 SDS

108481-83-0Relevant articles and documents

Shape-Selective Recognition of Quaternary Ammonium Chloride Ion Pairs

Li, Dong-Hao,Smith, Bradley D.

, p. 2808 - 2816 (2019/03/26)

Synthetic receptors that recognize ion pairs are potentially useful for many technical applications, but to date there has been little work on selective recognition of quaternary ammonium (Q+) ion pairs. This study measured the affinity of a tetralactam macrocycle for 11 different Q+·Cl- salts in chloroform solution. In each case, NMR spectroscopy was used to determine the association constant (Ka) and the structure of the associated complex. Ka was found to depend strongly on the molecular shape of Q+ and was enhanced when Q+ could penetrate the macrocycle cavity and engage in attractive noncovalent interactions with the macrocycle's NH residues and aromatic sidewalls. The highest measured Ka of 7.9 × 103 M-1 was obtained when Q+ was a p-CN-substituted benzylic trimethylammonium. This high-affinity Q+·Cl- ion pair was used as a template to enhance the synthetic yield of macrocyclization reactions that produce the tetralactam receptor or structurally related derivatives. In addition, a permanently interlocked rotaxane was prepared by capping the end of a noncovalent complex composed of the tetralactam macrocycle threaded by a reactive benzylic cation. The synthetic method provides access to a new family of rotaxanated ion pairs that can likely act as anion sensors, molecular shuttles, or transport molecules.

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