Active Chemical RecordCatalog PreviewCatalog ready

2,2,2-trifluoroethyl N-(4-ethylphenyl)carbamate

CAS 1087798-12-6Formula C11H12F3NO2MW 247.21PubChem 39871476

This compound is a trifluoroethyl carbamate derivative featuring an ethylphenyl moiety. It serves as a functionalized intermediate in organic synthesis, valuable for research and development applications requiring the incorporation of this specific chemical structure.

Loading RDKit molecule structure...
InChIKey: UDVWOUNGXJQXOG-UHFFFAOYSA-NC11H12F3NO2 | MW 247.21

Chemical Identity

Molecular Formula

C11H12F3NO2

Molecular Weight

247.21 g/mol

Exact Mass

247.082013

PubChem CID

39871476

SMILES String

CCc1ccc(NC(=O)OCC(F)(F)F)cc1

Names & Synonyms

2,2,2-trifluoroethyl 4-ethylphenylcarbamate2,2,2-Trifluoroethyl (4-ethylphenyl)carbamate2,2,2-trifluoroethylN-(4-ethylphenyl)carbamateZ381542352
External Identifiers
DTXSID701245331MTB79812AKOS009101866EN300-88299

Catalog Overview

2,2,2-Trifluoroethyl N-(4-ethylphenyl)carbamate, identified by CAS number 1087798-12-6 and molecular formula C11H12F3NO2, is an organic compound featuring a trifluoroethyl group linked via a carbamate to a 4-ethylphenyl moiety. This structural arrangement positions it as a versatile functionalized intermediate in organic synthesis. The presence of the trifluoromethyl group can confer distinct chemical properties, such as enhanced lipophilicity and metabolic stability, which are often advantageous in medicinal chemistry and materials science research.

Use Context

  • Research chemical sourcing
  • Custom synthesis and catalog availability review
  • COA, SDS, pricing, and fulfillment workflow

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White to off-white crystalline powder

Physical State

Solid

Melting Point

85.0 °C

Boiling Point

281.0 °C

Density

1.23 g/cm³

Water Solubility

Slightly soluble

Flash Point

170.9 °C

Applications / Classifications

Research intermediateCustom synthesis building block

Biological Target Reference

No verified biological target assignment. This compound is listed primarily as a research or synthetic intermediate.

Preliminary Safety-Style Reference

Preliminary

Preliminary safety-style information for reference only. Not a supplier SDS.

Handling and Storage
  • Handle 2,2,2-trifluoroethyl N-(4-ethylphenyl)carbamate in a well-ventilated area or fume hood. Always wear appropriate personal protective equipment, including safety glasses, chemical-resistant gloves, and a lab coat, to prevent skin and eye contact. Avoid inhalation of dust or vapors. In case of exposure, rinse affected areas thoroughly with water and seek medical attention if irritation persists. Store the compound in a cool, dry place, securely sealed and away from incompatible materials. This product is intended for research use only and is not for human or animal therapeutic or diagnostic use.

Related Products / Graph Discovery

Related products, derivatives, keywords, and application cues for catalog discovery.

Related products and analog discovery will be available as catalog graph data is expanded.