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CAS 51479-73-3

Allyl 2,2,2-Trichloroacetimidate TCI A2186

Allyl 2,2,2-Trichloroacetimidate TCI A2186

Chemical Identity

CAS No.
51479-73-3
PubChem
CID 316905·SID 125307218
Formula
C5H6Cl3NO
Molecular weight
202.46 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
prop-2-enyl 2,2,2-trichloroethanimidate
SMILES
C=CCOC(=N)C(Cl)(Cl)Cl
InChIKey
UJYZRNWTLPBNOR-UHFFFAOYSA-N
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Allyl 2,2,2-Trichloroacetimidate is a chemical compound widely used as a building block in the synthesis of complex organic molecules. This reagent plays a crucial role in laboratory settings, particularly in organic chemistry research, where it is employed to construct intricate molecular structures. Its unique chemical structure enables it to participate in highly specific chemical reactions, especially in coupling reactions with various functional groups. This makes it an essential component for chemists aiming to develop new compounds, pharmaceuticals, and materials.

The compound is favored for its reactivity and specificity, which allow for precise control over reaction outcomes. It exhibits stability under certain conditions, making it suitable for reactions that require controlled environments. Additionally, its solubility in organic solvents such as ethyl acetate and chloroform enhances its usability in laboratory processes. These properties make it a reliable choice for both academic and industrial research.

In Indonesian laboratories, Allyl 2,2,2-Trichloroacetimidate is commonly used in organic chemistry research, especially in institutions focused on drug development and material science. Its versatility and effectiveness in various synthetic pathways have made it a staple in many research projects. The compound is particularly valuable for its ability to facilitate the formation of complex molecular architectures, supporting advancements in chemical synthesis and innovation.

TCI brochures (PDF)

  • Organic synthesis of heterocyclic compounds due to its ability to form stable intermediates in coupling reactions.
  • Development of pharmaceuticals through its role in constructing complex molecular frameworks with high specificity.
  • Preparation of functionalized organic molecules by reacting with various functional groups under controlled conditions.
  • Research in material science for the synthesis of polymers and advanced chemical materials.
  • Analytical chemistry applications where precise chemical reactions are required for compound characterization.

Brand TCI
CAS number 51479-73-3
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities as per supplier specifications
Physical form Liquid or solid, depending on formulation and packaging
Storage Store in a cool, dry place away from moisture and direct sunlight

Allyl 2,2,2-Trichloroacetimidate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated laboratory setting, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with strong bases, alkali metals, and organic solvents that may trigger unwanted reactions. The compound is best stored in glass or polyethylene containers to ensure compatibility and prevent degradation. Always follow standard laboratory safety protocols when working with this reagent to ensure safe and effective use.

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