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

88554-07-8

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88554-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88554-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,5 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88554-07:
(7*8)+(6*8)+(5*5)+(4*5)+(3*4)+(2*0)+(1*7)=168
168 % 10 = 8
So 88554-07-8 is a valid CAS Registry Number.

88554-07-8SDS

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 1,4,8,11-tetrabenzyl-1,4,8,11-tetrazacyclotetradecane

1.2 Other means of identification

Product number -
Other names 1,4,8,11-Tetraazacyclotetradecane,1,4,8,11-tetrakis(phenylmethyl)

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:88554-07-8 SDS

88554-07-8Downstream Products

88554-07-8Relevant academic research and scientific papers

Metal Complexes with Macrocyclic Ligands. Part XXXVIII. Steric Effects in the Copper(II) and Nickel(II) Complexes with Tetra-N-alkylated 1,4,8,11-Tetraazacyclotetradecanes

Oberholzer, Martin R.,Neuburger, Markus,Zehnder, Margareta,Kaden, Thomas A.

, p. 505 - 513 (1995)

A series of tetra-N-alkylated 1,4,8,11-tetraazacyclotetradecanes have been synthesized and their complexation potential towards Ni2+ and Cu2+ studied.In the case of sterically demanding alkyl substituents, such as i-Pr, PhCH2, or 2-M

A direct method for the N-tetraalkylation of azamacrocycles

Counsell, Andrew J.,Jones, Angus T.,Todd, Matthew H.,Rutledge, Peter J.

, p. 2457 - 2461 (2016/12/09)

An efficient protocol for the direct synthesis of N-tetraalkylated derivatives of the azamacrocycles cyclam and cyclen has been developed, using a partially miscible aqueous-organic solvent system with propargyl bromide, benzyl bromide, and related halide

1,4,8,11-Tetraazabicyclo[9.3.1]pentadecanes: Synthesis and Use of a New Strategy for the Selective cis -N4,N8-Difunctionalization of Cyclam Derivatives

Guilard, Roger,Bessmertnykh, Alla G.,Beletskaya, Irina P.

, p. 1190 - 1192 (2007/10/03)

A new efficient route to derivatives of 1,4,8,11-tetraazabicyclo[9.3.1]pentadecane 2 and their use in a procedure of selective N4,N8-difunctionalization of cyclam is reported.

Cation-binding Properties of New Armed Macrocyclic Host Molecules and Their Applications to Phase-transfer Reactions and Cation Membrane Transport

Tsukube, Hiroshi,Takagi, Kentaro,Higashiyama, Tatsuo,Iwachido, Tadashi,Hayama, Naomi

, p. 1033 - 1038 (2007/10/02)

A new series of armed macrocyclic host molecules was prepared; the macrocycles were characterized by parent macrocyclic ligands and cation-ligating donor arms.Their cation-binding properties were significantly controlled by co-ordination characteristics od their parent macro-ring and donor sidearms, and chemical modifications of their basic structures provided interesting chemical functions.For example, a furan-bearing double armed crown ether showed high catalytic activity in some phase-transfer reactions; a multi-armed cyclam containing furan-oxygen atoms discriminated NH4(1+) ion from K(1+) and other related cations effectively.Such chemical functions of these armed macrocycles were not attained with common crown ethers and cryptands.Hence, further variations of ligand structures may lead to a new series of host molecules showing unique and important chemical functions.

Proton-assisted Transport of Amino Acid and Related Polycarboxylate Anions via Polyammonium Macrocycles

Tsukube, Hiroshi

, p. 615 - 620 (2007/10/02)

Anion-binding and transport properties of polyamine macrocycles have been examinated by liquid-liquid extraction and liquid membrane transport experiments.Some lipophilic polyamine macrocycles showed excellent transport properties, especially for polycarb

Specific Cation-transport Abilities of New Macrocyclic Polyamine Compounds

Tsukube, Hiroshi

, p. 970 - 971 (2007/10/02)

The lipophilic macrocyclic polyamine carriers (1) and (2) mediated efficient ammonium-cation transport with characteristic properties not observed in previously reported crown ether systems.

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