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1,4,8,11-Tetraazacyclotetradecane, 1,4,8,11-tetrakis[(trifluoroMethyl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96455-17-3

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96455-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96455-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,4,5 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96455-17:
(7*9)+(6*6)+(5*4)+(4*5)+(3*5)+(2*1)+(1*7)=163
163 % 10 = 3
So 96455-17-3 is a valid CAS Registry Number.

96455-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tetra(trifluoromethylsulfonyl)-1,4,8,11-tetraazocyclodecane

1.2 Other means of identification

Product number -
Other names 1,4,8,11-Tetra(trifluoromethylsulfonyl)-1,4,8,11-tetraazacyclotetradecane

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:96455-17-3 SDS

96455-17-3Relevant academic research and scientific papers

Aza compounds as anion receptors

-

, (2008/06/13)

A family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of Li+ ion in alkali metal batteries.

Triflamides for protection and cyclization of tetraamines to tetraazamacrocycles

Panetta,Yaouanc,Handel

, p. 5505 - 5508 (2007/10/02)

A facile two-step synthesis of tetraazamacrocycles is reported starting from trifluoromethanesulfonyl derivatives of linear tetraamines. After cyclization, the macrocycle was deprotected using sodium in liquid ammonia.

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