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2,2,2-Trifluoroethyl N-(1-methylpropyl)carbamate

CAS 1221725-57-0Formula C7H12F3NO2MW 199.17PubChem 47002264

This compound is a trifluoroethyl carbamate derivative, specifically 2,2,2-Trifluoroethyl N-(1-methylpropyl)carbamate. It is characterized by a trifluoroethyl group and a sec-butyl carbamate moiety. It serves as a functionalized intermediate in organic synthesis.

Loading RDKit molecule structure...
InChIKey: CCZXUOWSNIENSE-UHFFFAOYSA-NC7H12F3NO2 | MW 199.17

Chemical Identity

Molecular Formula

C7H12F3NO2

Molecular Weight

199.17 g/mol

Exact Mass

199.082013

PubChem CID

47002264

IUPAC Name

2,2,2-trifluoroethyl N-butan-2-ylcarbamate

SMILES String

CCC(C)NC(=O)OCC(F)(F)F

Names & Synonyms

2,2,2-trifluoroethyl N-(butan-2-yl)carbamateCCZXUOWSNIENSE-UHFFFAOYSA-N2,2,2-Trifluoroethyl butan-2-ylcarbamate2,2,2-trifluoroethylN-(butan-2-yl)carbamateZ858038256
External Identifiers
RefChem:242558DTXSID901239326AKOS011047766EN300-56575

Catalog Overview

2,2,2-Trifluoroethyl N-(1-methylpropyl)carbamate, with CAS 1221725-57-0 and molecular formula C7H12F3NO2, is a chemical compound featuring a 2,2,2-trifluoroethyl ester linked to an N-(1-methylpropyl)carbamate group. This structure makes it a valuable functionalized intermediate, particularly in the synthesis of more complex molecules where the trifluoroethyl group can impart specific chemical properties, such as increased lipophilicity or altered electronic characteristics. Its carbamate functionality also offers opportunities for further derivatization or use as a protecting group.

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

Colorless liquid

Physical State

Liquid

Melting Point

-10.0 °C

Boiling Point

225.0 °C

Density

1.16 g/cm³

Water Solubility

Slightly soluble

Flash Point

122.3 °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-(1-methylpropyl)carbamate in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including safety goggles, gloves, and a lab coat, to prevent skin and eye contact. Avoid inhalation of dust or vapors. In case of contact, rinse thoroughly with water. Consult the Safety Data Sheet (SDS) for detailed hazard information and safe handling procedures. Store in a cool, dry place, away from incompatible materials.

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