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1,4,7,10-Tetraazacyclotridecane, 12-[(4-nitrophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128924-90-3

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128924-90-3 Usage

Structure

Macrocyclic tetraamine with a 12-membered ring and a 4-nitrobenzyl moiety attached to one of the nitrogen atoms

Function

Chelating agent for metal ions

Applications

a. Catalysis
b. Coordination chemistry
c. Bioinorganic chemistry

Advantages

a. Stable and rigid structure
b. Forms stable complexes with metal ions

Potential uses

a. Medicinal and pharmaceutical applications
b. Development of metal-based drugs for cancer treatment

Versatility

Significant potential for various scientific and industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 128924-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,9,2 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 128924-90:
(8*1)+(7*2)+(6*8)+(5*9)+(4*2)+(3*4)+(2*9)+(1*0)=153
153 % 10 = 3
So 128924-90-3 is a valid CAS Registry Number.

128924-90-3SDS

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 12-[(4-nitrophenyl)methyl]-1,4,7,10-tetrazacyclotridecane

1.2 Other means of identification

Product number -
Other names -

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:128924-90-3 SDS

128924-90-3Relevant academic research and scientific papers

Accelerating water exchange for GDIII chelates by steric compression around the water binding site

Ruloff, Robert,Toth, Eva,Scopelliti, Rosario,Tripier, Raphael,Handel, Henri,Merbach, Andre E.

, p. 2630 - 2631 (2002)

The water exchange process was accelerated for nine-coordinate, monohydrated macrocyclic GdIII complexes by inducing steric compression around the water binding site; the increased steric crowding was achieved by replacing an ethylene bridge of

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