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CAS 2557-13-3

Methyl 3-(Trifluoromethyl)benzoate TCI M1718

Methyl 3-(Trifluoromethyl)benzoate TCI M1718

Chemical Identity

CAS No.
2557-13-3
PubChem
CID 520213·SID 87558622
Formula
C9H7F3O2
Molecular weight
204.15 g/mol
Purity
>98.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 3-(trifluoromethyl)benzoate
SMILES
COC(=O)C1=CC(=CC=C1)C(F)(F)F
InChIKey
QQHNNQCWKYFNAC-UHFFFAOYSA-N
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Methyl 3-(Trifluoromethyl)benzoate is a chemical compound widely used in organic reactions, particularly in the synthesis of fluorinated compounds. This compound plays a crucial role in laboratory settings where fluorination is required, serving as a key building block for the development of various organic materials. Its unique molecular structure, featuring a trifluoromethyl group, imparts specific chemical properties that make it valuable for advanced chemical research. Due to its stability and controlled reactivity, it is frequently used in synthetic pathways that demand precision and reliability.

The compound is known for its exceptional chemical stability and solubility in organic solvents, which makes it ideal for use in a wide range of experimental conditions. These properties ensure that it remains effective even under varying laboratory environments. Its controlled reactivity also allows chemists to manipulate it with greater accuracy, reducing the risk of unwanted side reactions. This combination of stability and reactivity makes it a preferred choice for researchers working in both academic and industrial settings.

In Indonesian laboratories, Methyl 3-(Trifluoromethyl)benzoate is commonly utilized in organic chemistry research, especially in pharmaceutical and materials science applications. Many research institutions and universities in Indonesia rely on this compound for its versatility and reliability. Its availability in various packaging formats ensures that it can be used in both small-scale and large-scale experiments, making it a practical choice for a wide range of chemical investigations.

TCI brochures (PDF)

  • Organic synthesis in pharmaceutical research due to its fluorinated structure and controlled reactivity.
  • Fluorination reactions in materials science for the development of advanced polymers and coatings.
  • Structural modification of aromatic compounds in academic research for the study of fluorinated derivatives.
  • Intermediate in the production of specialty chemicals used in industrial applications requiring fluorine substitution.
  • Support for synthetic pathways in academic laboratories focusing on fluorinated organic compounds.

Brand TCI
CAS number 2557-13-3
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes Available in various packaging formats for different experimental scales
Physical form Solid
Storage —

Methyl 3-(Trifluoromethyl)benzoate should be stored in a cool, dry place away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Due to its chemical stability, it does not require special refrigeration but should be protected from potential contaminants. In laboratory settings, it is important to handle the compound with appropriate personal protective equipment to ensure safety. Proper labeling and storage conditions help maintain its integrity and ensure safe usage in all experimental applications.

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