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N-hexyl-2-iodoacetamide is an organic compound with the chemical formula C8H16INO. It is a derivative of iodoacetamide, featuring a hexyl chain attached to the nitrogen atom. N-hexyl-2-iodoacetamide is primarily used as a chemical reagent in various organic synthesis processes, particularly in the preparation of pharmaceuticals and other specialty chemicals. Its structure allows for the introduction of iodine-containing functional groups into target molecules, which can be crucial for the development of new drugs or materials with specific properties. N-hexyl-2-iodoacetamide is also known for its potential applications in the field of radiopharmaceuticals, where it can be used to label compounds for imaging studies.

5345-63-1

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5345-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5345-63-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5345-63:
(6*5)+(5*3)+(4*4)+(3*5)+(2*6)+(1*3)=91
91 % 10 = 1
So 5345-63-1 is a valid CAS Registry Number.

5345-63-1SDS

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 N-HEXYL-2-IODOACETAMIDE

1.2 Other means of identification

Product number -
Other names N-(indol-3-yl-phenyl-methyl)-N-p-tolyl-benzamide

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:5345-63-1 SDS

5345-63-1Downstream Products

5345-63-1Relevant academic research and scientific papers

Complexes of selected late period lanthanide(III) cations with 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid amide (DOTAM)-alkyl ligands-A new platform for the development of paramagnetic chemical exchange saturation transfer (PARACEST) magnetic resonance imaging (MRI) contrast agents

Elmehriki, Adam A.H.,Milne, Mark,Suchy, Mojmir,Bartha, Robert,Hudson, Robert H.E.

, p. 211 - 219 (2013)

A series of 18 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid amide (DOTAM)-alkyl derived complexes with selected late lanthanide(III) cations (Dy3+, Tb3+, and Tm3+) has been synthesized; their magnetic properties have been evaluated and compared to those derived from DOTAM. Peralkylation of cyclen with corresponding N-iodoacetyl amines was utilized as the key step in the synthesis. Chemical exchange saturation transfer (CEST) spectra of the complexes have been acquired at 37 C, revealing that Tm3+-derived DOTAM-alkyl complexes possess the most favorable properties as potential paramagnetic chemical exchange saturation transfer (PARACEST) magnetic resonance imaging (MRI) contrast agents.

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