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tert-Butyl (S)-(1-fluoro-3-methylbutan-2-yl)carbamate

CAS 2761418-78-2Formula C10H20FNO2MW 205.27PubChem 102082035

tert-Butyl (S)-(1-fluoro-3-methylbutan-2-yl)carbamate is a fluorinated, Boc-protected amino acid derivative with a molecular formula of C10H20FNO2 and a molecular weight of 205.27. This chiral compound is primarily utilized in synthetic organic chemistry as a functionalized intermediate for the synthesis of more complex molecules in research settings.

Loading RDKit molecule structure...
InChIKey: NYIZQMGKPXMKPN-MRVPVSSYSA-NC10H20FNO2 | MW 205.27

Chemical Identity

Molecular Formula

C10H20FNO2

Molecular Weight

205.27 g/mol

Exact Mass

205.147807

PubChem CID

102082035

IUPAC Name

tert-butyl N-[(2S)-1-fluoro-3-methylbutan-2-yl]carbamate

SMILES String

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

Names & Synonyms

(S)-N-Boc-1-fluoro-3-methyl-2-butylamineC10H20FNO2tert-butyl N-[(1S)-1-(fluoromethyl)-2-methyl-propyl]carbamate
External Identifiers
MFCD30378946AKOS037629672SY046676CS-0514403

Catalog Overview

tert-Butyl (S)-(1-fluoro-3-methylbutan-2-yl)carbamate, identified by CAS 2761418-78-2, is a precisely structured organic compound featuring a tert-butyl carbamate (Boc) protecting group on an amino functionality, a fluorine atom, and an (S)-chiral center. Its molecular formula is C10H20FNO2 and it has a molecular weight of 205. 27. As a functionalized intermediate, it is valuable in the synthesis of various pharmaceutical candidates and agrochemicals, particularly where the introduction of a chiral fluorinated amino group is desired.

Use Context

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

tert-Butyl (S)-(1-fluoro-3-methylbutan-2-yl)carbamate, identified by CAS 2761418-78-2, is a precisely structured organic compound featuring a tert-butyl carbamate (Boc) protecting group on an amino functionality, a fluorine atom, and an (S)-chiral center. Its molecular formula is C10H20FNO2 and it has a molecular weight of 205.27. As a functionalized intermediate, it is valuable in the synthesis of various pharmaceutical candidates and agrochemicals, particularly where the introduction of a chiral fluorinated amino group is desired. Its Boc protection allows for selective manipulation of other functional groups during multi-step syntheses for research purposes.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

Colorless liquid

Physical State

Liquid

Melting Point

5.0 °C

Boiling Point

220.0 °C

Density

1.05 g/cm³

Water Solubility

Slightly soluble

Flash Point

85.0 °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
  • For research use only. Handle tert-Butyl (S)-(1-fluoro-3-methylbutan-2-yl)carbamate in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Avoid inhalation, ingestion, and skin contact. Refer to the Safety Data Sheet (SDS) for detailed hazard information and safe handling procedures. Store in a cool, dry place, away from incompatible materials.

Related Products / Graph Discovery

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

Similar products (text references)

2580201-79-0CAS 2580201-79-0

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.