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111514-29-5

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111514-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111514-29-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,1 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111514-29:
(8*1)+(7*1)+(6*1)+(5*5)+(4*1)+(3*4)+(2*2)+(1*9)=75
75 % 10 = 5
So 111514-29-5 is a valid CAS Registry Number.

111514-29-5SDS

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 1,4,8,11-Tetrakis(toluene-p-sulphonyl)-1,4,8,11-tetraazaundecane

1.2 Other means of identification

Product number -
Other names .1,4,8,11-Tetra(p-toluenesulfonyl]-1,4,8,11-tetraazaundecane

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:111514-29-5 SDS

111514-29-5Relevant articles and documents

SYNTHESIS AND COMPLEXING PROPERTIES OF 1,5,8,12-TETRAKIS(DIHYDROXYPHOSPHORYLMETHYL)-1,5,8,12-TETRAAZACYCLOTETRADECANE, A CYCLOPENDANT PHOSPHORORGANIC COMPLEXON

Pisareva, S. A.,Bel'skii, F. I.,Medved', T. Ya.,Kabachnik, M. I.

, p. 372 - 376 (1987)

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Equilibrium and kinetic properties of CuII cyclophane complexes: The effect of changes in the macrocyclic cavity caused by changes in the substitution at the aromatic ring

Verdejo, Begona,Basallote, Manuel Garcia,Ferrer, Armando,Manez, Maria Angeles,Hernandez, Juan Carlos,Chadim, Martin,Hodacova, Jana,Llinares, Jose Miguel,Soriano, Conxa,Garcia-Espana, Enrique

experimental part, p. 1497 - 1507 (2009/02/07)

The o-B232, m-B232 and p-B232 cyclophanes result from attaching the terminal amine groups of 1,4,8,11-tetraazaundecane (232) to the benzylic carbons of the corresponding o-, m- or p-xylanes. The cavity size of these cyclophanes changes moderately as a con

Methods of preparing manganese complexes of nitrogen-containing macrocyclic ligands

-

, (2008/06/13)

The present invention is directed to low molecular weight mimics of superoxide dismutase (SOD) represented by the formula: STR1 wherein R, R', R1, R'1, R2, R'2, R3, R'3, R4, R'4, R5, R'5, R6, R'6, R7, R'7, R8, R'8, R9, and R'9 and X, Y, Z and n are as defined herein, useful as therapeutic agents for inflammatory disease states and disorders, ischemic/reperfusion injury, stroke, atherosclerosis, hypertension and all other conditions of oxidant-induced tissue damage or injury.

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