4-Methoxybenzyl 2,2,2-Trichloroacetimidate TCI M2016

Chemical Identity

CAS No.: 89238-99-3
PubChem: CID 11087263·SID 87560864
Formula: C10H10Cl3NO2
Molecular weight: 282.5 g/mol
Purity: >96.0%(GC)
Reference databases: ChemSpider

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (4-methoxyphenyl)methyl 2,2,2-trichloroethanimidate
SMILES: COC1=CC=C(C=C1)COC(=N)C(Cl)(Cl)Cl
InChIKey: TYHGKLBJBHACOI-UHFFFAOYSA-N

Rp 2.782.500,00

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The TCI M2016 89238-99-3 4-Methoxybenzyl 2,2,2-Trichloroacetimidate is a synthetic reagent widely used in laboratory settings for the formation of C-X (non-halogen) bonds. This compound plays a crucial role in organic synthesis by acting as a versatile electrophilic reagent. It is commonly employed in substitution reactions and the construction of complex molecular structures. Its unique chemical structure allows it to participate in various reaction mechanisms, making it an essential tool for chemists working in both academic and industrial environments.

One of the key properties that make this reagent a preferred choice is its high reactivity and solubility in organic solvents such as ethyl acetate and chloroform. These characteristics facilitate efficient dissolution and reaction processes, ensuring consistent results in synthetic procedures. Additionally, the compound's stability under controlled conditions contributes to its reliability in laboratory applications. Its ability to function as a donor in nucleophilic substitution reactions further enhances its utility in a wide range of chemical transformations.

In Indonesian laboratories, this reagent is highly relevant for research in organic chemistry, pharmacology, and materials science. It is frequently used in the development of new compounds, drug synthesis, and the study of heterocyclic and aromatic structures. Many research institutions and universities in Indonesia rely on this compound for its precision and effectiveness in complex synthetic processes. Its availability through AMI Scientific ensures that Indonesian researchers have access to high-quality reagents for their scientific endeavors.

Related TCI products

Organic synthesis for the formation of C-X bonds in complex molecule construction due to its electrophilic nature and reactivity.
Drug development and pharmaceutical research as it supports the synthesis of aromatic and heterocyclic compounds.
SN1 and SN2 reaction mechanisms where it acts as a good electrophilic substrate for nucleophilic attack.
Material science applications in the creation of advanced polymers and functional materials through controlled chemical reactions.
Academic research in universities and research institutes for teaching and experimental purposes in synthetic chemistry.

Brand	TCI
CAS number	89238-99-3
Molecular formula	—
Purity	—
Category	Chemistry > Synthetic Reagents > C-X(Non-Halogen) Bond Formation [Synthetic Reagents]
Pack sizes	Available in standard chemical reagent packaging sizes
Physical form	Solid or liquid depending on formulation and supplier specifications
Storage	—

This reagent should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and maintain chemical integrity. Due to its reactivity, it should be handled with appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to moisture and incompatible substances to ensure safe storage. In laboratory settings, it is important to follow standard operating procedures for chemical handling to minimize risks and ensure compliance with safety regulations.

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