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N-[2-Iodoethyl]trifluoroacetamide|23023|67680-56-2

N-[2-Iodoethyl]trifluoroacetamide

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Sku CI23023_250_MG
Chem Impex
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Product Information

Product Name
N-2-Iodoethyltrifluoroacetamide
Brand Name
Chem Impex
Product Number
23023
CAS
67680-56-2
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
587696
IUPAC Name
2,2,2-trifluoro-N-(2-iodoethyl)acetamide
InChI Key
QFRHEHPVTSCSIH-UHFFFAOYSA-N
SMILES
C(CI)NC(=O)C(F)(F)F

Description

N-2-Iodoethyltrifluoroacetamide is widely utilized in research focused on

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting specific biological pathways, enhancing drug efficacy.

Organic Synthesis: It is employed in organic chemistry for the introduction of trifluoroacetamide groups, which can improve the solubility and stability of compounds in various solvents.

Bioconjugation: The chemical is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, facilitating drug delivery systems and diagnostic applications.

Material Science: In the development of advanced materials, it acts as a functionalizing agent, enhancing the properties of polymers and coatings for better performance in industrial applications.

Analytical Chemistry: This compound is utilized in analytical methods to improve the detection and quantification of specific analytes, making it valuable in quality control and research laboratories.

References Data Source From Pubchem

Selectivity of labeled bromoethylamine for protein alkylation
Publication Name: Journal of Molecular Modeling
Publication Date: 2012-05-29
DOI: 10.1007/s00894-012-1461-9

In-Gel Derivatization of Proteins for Cysteine-Specific Cleavages and their Analysis by Mass Spectrometry
Publication Name: Journal of Proteome Research
Publication Date: 2002-12-24
DOI: 10.1021/pr025568g

Modification of Cysteine
Publication Name: Current Protocols in Protein Science
Publication Date: 1996-03
DOI: 10.1002/0471140864.ps1501s03

The Synthesis of Radioactive Photoaffinity Labels Containing Magnesium Tetrapyrrole Intermediates of Chlorophyll and Bacteriochlorophyll Biosynthesis
Publication Name: Current Research in Photosynthesis
Publication Date: 1990
DOI: 10.1007/978-94-009-0511-5_587

Schafer, E. W., Jr., and W. A. Bowles Jr. 2004. Toxicity, Repellency of Phytotoxicity of 979 Chemicals to Birds, Mammals and Plants. Research Report No. 04-01. National Wildlife Research Center, Fort Collins, Colorado. 118 pp. https://www.aphis.usda.gov/ws/nwrc/chem-effects-db/U_schafer041_2004.pdf