CAS 383-65-3

N-Allyl-2,2,2-trifluoroacetamide

Description:

N-Allyl-2,2,2-trifluoroacetamide, with the CAS number 383-65-3, is an organic compound characterized by the presence of a trifluoroacetamide functional group and an allyl substituent. This compound typically appears as a colorless to pale yellow liquid and is known for its distinctive trifluoromethyl group, which imparts unique chemical properties, including increased lipophilicity and stability. It is soluble in organic solvents such as dichloromethane and ether but has limited solubility in water due to its hydrophobic characteristics. N-Allyl-2,2,2-trifluoroacetamide can participate in various chemical reactions, including nucleophilic substitutions and polymerization processes, making it valuable in synthetic organic chemistry. Its trifluoromethyl group enhances its reactivity and can influence the electronic properties of the molecule, making it a useful building block in the synthesis of pharmaceuticals and agrochemicals. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.

Formula: C₅H₆F₃NO

InChI: InChI=1/C5H6F3NO/c1-2-3-9-4(10)5(6,7)8/h2H,1,3H2,(H,9,10)

SMILES: C=CCN=C(C(F)(F)F)O

Synonyms:

• N-Allyltrifluoroacetamide
• 2,2,2-trifluoro-N-(prop-2-en-1-yl)acetamide

N-Allyl-2,2,2-trifluoroacetamide

CAS: 383-65-3

N-Allyl-2,2,2-trifluoroacetamide

Purity: 95%

Molecular weight: 153.10g/mol

Ref: 54-PC101134

N-ALLYL-2,2,2-TRIFLUOROACETAMIDE

CAS: 383-65-3

Formula: C₅H₆F₃NO

Purity: 97%(stabilized with MEHQ)

Color and Shape: Liquid

Molecular weight: 153.104

Ref: 10-F330708