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tert-Butyl (R)-(1-fluoropropan-2-yl)carbamate

CAS 2006287-03-0Formula C8H16FNO2MW 177.22PubChem 129319737

tert-Butyl (R)-(1-fluoropropan-2-yl)carbamate is an enantiomerically pure, fluorinated carbamate, useful as a chiral building block in organic synthesis, particularly for pharmaceutical research.

Loading RDKit molecule structure...
InChIKey: LCYJCLXHXXANCJ-ZCFIWIBFSA-NC8H16FNO2 | MW 177.22

Chemical Identity

Molecular Formula

C8H16FNO2

Molecular Weight

177.22 g/mol

Exact Mass

177.116507

PubChem CID

129319737

IUPAC Name

tert-butyl N-[(2R)-1-fluoropropan-2-yl]carbamate

SMILES String

C[C@H](CF)NC(=O)OC(C)(C)C

Names & Synonyms

(R)-N-Boc-1-fluoro-2-propylamineAC5310(R)-tert-Butyl (1-fluoropropan-2-yl)carbamatetert-butyl N-[(1R)-2-fluoro-1-methyl-ethyl]carbamate
External Identifiers
MFCD30378923AKOS037629651SY046156CS-0435437EN300-22150350

Catalog Overview

tert-Butyl (R)-(1-fluoropropan-2-yl)carbamate, identified by CAS 2006287-03-0, is a chiral fluorinated carbamate derivative. It incorporates a tert-butyl carbamate protecting group on an (R)-1-fluoropropan-2-yl amine moiety. This compound is primarily utilized in research and development as a versatile chiral building block. Its fluorine atom and defined stereochemistry make it valuable for synthesizing complex molecules, including potential pharmaceutical intermediates and agrochemicals, where specific stereoisomers and fluorine incorporation are critical for biological activity or metabolic stability.

Use Context

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

tert-Butyl (R)-(1-fluoropropan-2-yl)carbamate, identified by CAS 2006287-03-0, is a chiral fluorinated carbamate derivative. It incorporates a tert-butyl carbamate protecting group on an (R)-1-fluoropropan-2-yl amine moiety. This compound is primarily utilized in research and development as a versatile chiral building block. Its fluorine atom and defined stereochemistry make it valuable for synthesizing complex molecules, including potential pharmaceutical intermediates and agrochemicals, where specific stereoisomers and fluorine incorporation are critical for biological activity or metabolic stability. It is suitable for various organic synthesis reactions requiring a protected chiral amine with a fluorine substituent.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

Colorless liquid

Physical State

Liquid

Melting Point

10.0 °C

Boiling Point

215.0 °C

Density

1.05 g/cm³

Water Solubility

Sparingly soluble

Flash Point

95.0 °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 with appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Use in a well-ventilated area or fume hood to avoid inhalation. Avoid contact with skin and eyes. In case of contact, rinse immediately with plenty of water. Store in a cool, dry place, away from incompatible materials. Consult the Safety Data Sheet (SDS) for detailed hazard information and safe handling procedures.

Related Products / Graph Discovery

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

Similar products (text references)

1393366-29-4CAS 1393366-29-4

Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 292419GHS Pictograms: GHS07Shipment review: Shipment details require review before fulfillment.

Compliance cues are non-linked reference tags and require shipment review.

Catalog navigation

Other public CAS pages in this catalog. These links support navigation across additional intermediates and do not imply equivalence, availability, or shared use.