Chemical Identity
Molecular Formula
C8H16BrNO2
Molecular Weight
238.12 g/mol
Exact Mass
237.03644
PubChem CID
14458310
IUPAC Name
tert-butyl N-(2-bromopropyl)carbamate
SMILES String
CC(Br)CNC(=O)OC(C)(C)C
Names & Synonyms
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External Identifiers
Catalog Overview
Tert-butyl (2-bromopropyl)carbamate, with CAS 121102-88-3 and molecular formula C8H16BrNO2, is a key functionalized intermediate in synthetic chemistry. It features a tert-butyl carbamate (Boc) protecting group on an amine, alongside a bromine atom on the propyl chain. This bifunctional nature makes it highly valuable for various synthetic transformations, including nucleophilic substitution reactions to introduce new functionalities, or as a precursor in the synthesis of more complex molecules. Its Boc group provides amine protection, which can be selectively removed under acidic conditions, allowing for controlled reactivity in...
Use Context
- Research chemical sourcing
- Custom synthesis and catalog availability review
- COA, SDS, pricing, and fulfillment workflow
Read more catalog context
Tert-butyl (2-bromopropyl)carbamate, with CAS 121102-88-3 and molecular formula C8H16BrNO2, is a key functionalized intermediate in synthetic chemistry. It features a tert-butyl carbamate (Boc) protecting group on an amine, alongside a bromine atom on the propyl chain. This bifunctional nature makes it highly valuable for various synthetic transformations, including nucleophilic substitution reactions to introduce new functionalities, or as a precursor in the synthesis of more complex molecules. Its Boc group provides amine protection, which can be selectively removed under acidic conditions, allowing for controlled reactivity in multi-step syntheses. This compound is intended for research use only.
Physical Data
EstimatedEstimated / predicted physical property values for catalog reference.
Appearance
White solid
Physical State
Solid
Melting Point
40.9 °C
Boiling Point
230.9 °C
Density
1.23 g/cm³
Water Solubility
0.0221 mol/L
Flash Point
133.8 °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 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. Always consult the Safety Data Sheet (SDS) for comprehensive safety information before use.
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