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1,4,7,10-Tetraazacyclododecane-1,4,7-triacetic acid, 10-[2-[[(phenylmethoxy)carbonyl]amino]ethyl]-, tris(1,1-dimethylethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

824984-74-9

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824984-74-9 Usage

Chemical structure

A complex organic compound with a cyclic structure containing four nitrogen atoms, three acetic acid groups, and three tert-butyl ester groups.

Functional groups

Contains an aminoethyl group with a phenylmethoxy carbonyl moiety.

Chelating agent

Used in medicinal chemistry for binding metal ions.

Applications

Potential use in radiopharmaceuticals, diagnostic imaging agents, contrast agents for magnetic resonance imaging (MRI), and treatment of various diseases.

Esterification

Esterified with three tert-butyl groups (1,1-dimethylethyl ester).

Molecular weight

Approximately 602.85 g/mol

Solubility

Soluble in organic solvents such as dimethyl sulfoxide (DMSO) and dimethylformamide (DMF).

Stability

Stable under normal temperature and pressure conditions.

Reactivity

Reacts with metal ions to form stable complexes.

Check Digit Verification of cas no

The CAS Registry Mumber 824984-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,9,8 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 824984-74:
(8*8)+(7*2)+(6*4)+(5*9)+(4*8)+(3*4)+(2*7)+(1*4)=209
209 % 10 = 9
So 824984-74-9 is a valid CAS Registry Number.

824984-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[N-(benzyloxycarbonyl)-2-aminoethyl]-1,4,7,10-tetraazacyclododecane-4,7,10-triacetic acid tri(1,1-dimethylethyl ester)

1.2 Other means of identification

Product number -
Other names 1-[N-(benzyloxycarbonyl)-2-aminoethyl]-1,4,7,10-tetraazacyclododecane-4,7,10-triacetic tris(1,1-dimethylethyl) ester

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:824984-74-9 SDS

824984-74-9Relevant academic research and scientific papers

Luminescent heptadentate Tb3+ complex with pendant aza-15-crown-5 showing recognition of lactate and salicylate in aqueous solution

Li, Cong,Wong, Wing-Tak

, p. 6055 - 6058 (2004)

The coordinatedly unsaturated neutral complex TbL1 that possesses two labile metal-bound water molecules provides linear response to lactate in the range of 0-3.0mM at the simulated extracellular background with the variations of Tb luminescence lifetime

Exofacial protein thiols as a route for the internalization of Gd(III)-based complexes for magnetic resonance imaging cell labeling

Digilio, Giuseppe,Menchise, Valeria,Gianolio, Eliana,Catanzaro, Valeria,Carrera, Carla,Napolitano, Roberta,Fedeli, Franco,Aime, Silvio

experimental part, p. 4877 - 4890 (2010/10/19)

Four novel MRI Gd(III)-based probes have been synthesized and evaluated for their labeling properties on cultured cell lines K562, C6, and B16. The labeling strategy relies upon the fact that cells display a large number of reactive exofacial protein thio

Poly-β-cyclodextrin based platform for pH mapping via a ratiometric 19F/1H MRI method

Gianolio, Eliana,Napolitano, Roberta,Fedeli, Franco,Arena, Francesca,Aime, Silvio

supporting information; experimental part, p. 6044 - 6046 (2010/11/03)

The in vitro validation of a new pH mapping MRI method based on a supramolecular poly-β-cyclodextrin-19F-Gd adduct is reported.

SYNTHESIS OF TRIS N-ALKYLATED 1,4,7,10-TETRAAZACYCLODODECANES

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Page 13; Fig. 6, (2008/06/13)

A directly synthetic method for preparing tris-alkylated 1,4,7,10-tetraazacyclododecanes by the reactions of 1,4,7,10-tetraazacyclododecane (cyclen) and appropriate electrophiles is accomplished in high yield. The method provides operational convenience,

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