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60147-29-7

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60147-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60147-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,4 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60147-29:
(7*6)+(6*0)+(5*1)+(4*4)+(3*7)+(2*2)+(1*9)=97
97 % 10 = 7
So 60147-29-7 is a valid CAS Registry Number.

60147-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,10,13-tris(p-tolylsulphonyl)-1,4-dioxa-7,10,13-triazacyclopentadecane

1.2 Other means of identification

Product number -
Other names 7,10,13-Tritosyl-1,4-dioxa-7,10,13-triazacyclopentadecan

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:60147-29-7 SDS

60147-29-7Downstream Products

60147-29-7Relevant articles and documents

Metal complexes of pentadentate macrocyclic ligands containing oxygen and nitrogen as donor atoms

Cabral

, p. 515 - 524 (2007/10/02)

Four macrocyclic ligands have been synthesized: 1-oxa-4,7,10,13-tetraazacyclopentadecane (1), 1,4-dioxa-7,10,13-triazacyclopentadecane (2), 1,4-dioxa-7,11,14-triazacyclohexadecane (3), 1,4-dioxa-7,11,15-triazacycloheptadecane (4), one of them, 3, for the first time. The protonation constants of the ligands and the stability constants of the complexes formed by the four ligands with some divalent first-series transition-metal ions, Cd2+ and Pb2+, were determined by potentiometric methods, in aqueous solution, at 25° and I = 0.10 M (KNO3). The sequence of protonation of ligand 1 was studied by 1H-NMR spectroscopy. The Irving-Williams' order of stability is obeyed for the complexes of all the ligands, and the metal complexes of 1 present the higher values of stability. A drop in the stability of all the metal complexes studied is observed when the metal complexes of 1 are compared with the corresponding complexes of 2. The effect of the increase of the ring size of the macrocycle can be observed for metal complexes of the series of ligands 2-4, where, in spite of the slight increase of the overall basicity of the ligands (20.28, 22.25, and 24.96 for 2, 3, and 4 respectively), small differences in stability are found for the corresponding complexes of 2 and 3, but a significant drop occurs for all the metal complexes formed with the 17-membered ligand, specially for the larger metal ions like Mn2+ and Pb2+.

MACROHETEROCYCLES. PART 44. FACILE SYNTHESIS OF AZACROWN ETHERS AND CRYPTANDS IN A TWO-PHASE SYSTEM

Lukyanenko, Nikolai G.,Basok, Stepan S.,Filonova, Lyubov K.

, p. 3141 - 3148 (2007/10/02)

A facile procedure is proposed for the preparation of azacrown ethers and cryptands by condensation of dibromides or ethylene glycol bis(toluene-p-sulphonate)s with acyclic bis(sulphonamide)s or with bisdiazacrown ethers, respectively.The reaction was carried out in a two-phase system of aqueous alkali-toluene (benzene)in the presence of quaternary ammonium salts as phase transfer catalysts.The catalytic activity decreased in the sequence: Bu4NI ca.Bu4NBr > Bu4NCl > Bu4NHSO4 > Et3NCH2C6H5NCl.Maximum yields of twelve-membered azacrown ethers are obtained when lithium hydroxide is used, while crown ethers of larger size are observed in the presence of sodium or potassium hydroxides; this may be due to a template effect.

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