Chemical Identity
Molecular Formula
C12H24BrNO2
Molecular Weight
294.23 g/mol
Exact Mass
293.09904
PubChem CID
155978267
SMILES String
CC(C)C[C@@H](CCBr)NC(=O)OC(C)(C)C
External Identifiers
Catalog Overview
tert-butyl N-[(3S)-1-bromo-5-methylhexan-3-yl]carbamate is a chiral, brominated organic compound featuring a tert-butyl carbamate (Boc) protecting group and an isobutyl moiety. With a bromine atom and a protected amine, this compound serves as a versatile building block in organic synthesis. Its specific (3S) stereochemistry makes it particularly useful for constructing complex chiral molecules, including potential pharmaceutical intermediates and agrochemicals, where precise stereocontrol is essential. This chemical is intended for Research Use Only (RUO).
Use Context
- Research chemical sourcing
- Custom synthesis and catalog availability review
- COA, SDS, pricing, and fulfillment workflow
Physical Data
EstimatedEstimated / predicted physical property values for catalog reference.
Appearance
Colorless liquid
Physical State
Liquid
Melting Point
5.0 °C
Boiling Point
270.0 °C
Density
1.2 g/cm³
Water Solubility
Insoluble
Flash Point
135.0 °C
Applications / Classifications
Biological Target Reference
No verified biological target assignment. This compound is listed primarily as a research or synthetic intermediate.
Preliminary Safety-Style Reference
PreliminaryPreliminary safety-style information for reference only. Not a supplier SDS.
Handling and Storage
- Handle tert-butyl N-[(3S)-1-bromo-5-methylhexan-3-yl]carbamate in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including chemical-resistant gloves, safety glasses or goggles, and a lab coat. Avoid inhalation of dust or vapors, ingestion, and direct skin or eye contact. In case of contact, rinse immediately with plenty of water and seek medical advice. Always refer to the Safety Data Sheet (SDS) for comprehensive safety information and handling procedures.
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.