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tert-butyl N-[(2R)-3-bromo-2-methylpropyl]carbamate

CAS 848818-71-3Formula C9H18BrNO2MW 252.15PubChem 86601426

tert-butyl N-[(2R)-3-bromo-2-methylpropyl]carbamate is a chiral bromo-substituted carbamate primarily used in organic synthesis as a versatile building block. Its (2R) stereochemistry makes it valuable for introducing protected amine and bromo functionalities into target molecules, particularly in the synthesis of enantiomerically pure compounds for research purposes.

Loading RDKit molecule structure...
InChIKey: HYTMOLGBQNHTPA-ZETCQYMHSA-NC9H18BrNO2 | MW 252.15

Chemical Identity

Molecular Formula

C9H18BrNO2

Molecular Weight

252.15 g/mol

Exact Mass

251.05209

PubChem CID

86601426

SMILES String

C[C@@H](CBr)CNC(=O)OC(C)(C)C

Names & Synonyms

tert-butyl N-((2R)-3-bromo-2-methylpropyl)carbamate966-433-0HYTMOLGBQNHTPA-ZETCQYMHSA-N(R)-(3-Bromo-2-methyl-propyl)-carbamic acid tert-butyl ester
External Identifiers
RefChem:894890SCHEMBL6518299EN300-27143426

Catalog Overview

tert-butyl N-[(2R)-3-bromo-2-methylpropyl]carbamate, identified by CAS 848818-71-3, is an enantiomerically pure organic compound with the molecular formula C9H18BrNO2 and a molecular weight of 252. 15 g/mol. It features a tert-butyl carbamate protecting group on an amine and a bromo substituent on a methylpropyl chain, with a defined (2R) stereocenter. This structure classifies it as a functionalized intermediate, making it a key reagent in the synthesis of complex organic molecules.

Use Context

  • Research chemical sourcing
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  • COA, SDS, pricing, and fulfillment workflow
Read more catalog context

tert-butyl N-[(2R)-3-bromo-2-methylpropyl]carbamate, identified by CAS 848818-71-3, is an enantiomerically pure organic compound with the molecular formula C9H18BrNO2 and a molecular weight of 252.15 g/mol. It features a tert-butyl carbamate protecting group on an amine and a bromo substituent on a methylpropyl chain, with a defined (2R) stereocenter. This structure classifies it as a functionalized intermediate, making it a key reagent in the synthesis of complex organic molecules. The bromo group serves as a reactive site for various coupling reactions, nucleophilic substitutions, or elimination reactions, while the Boc-protected amine allows for selective deprotection and further functionalization. Its chiral nature is crucial for applications requiring stereoselective synthesis.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

white solid

Physical State

solid

Melting Point

30.5 °C

Boiling Point

260.6 °C

Density

1.22 g/cm³

Water Solubility

3.39 × 10⁻³ mol/L

Flash Point

120.1 °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 tert-butyl N-[(2R)-3-bromo-2-methylpropyl]carbamate in a well-ventilated fume hood. Wear appropriate personal protective equipment, including chemical-resistant gloves, safety goggles, and a lab coat. Avoid inhalation of dust or vapors and direct 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 comprehensive safety information before use.

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