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(R)-Benzyl (1-bromobut-3-en-2-yl)carbamate

CAS 1271983-91-5Formula C12H14BrNO2MW 284.15PubChem 49786989

(R)-Benzyl (1-bromobut-3-en-2-yl)carbamate is a chiral organobromine compound featuring a carbamate protecting group and an alkene, primarily used as a versatile building block in organic synthesis for research purposes.

Loading RDKit molecule structure...
InChIKey: OWAMYAOUOXTLCN-LLVKDONJSA-NC12H14BrNO2 | MW 284.15

Chemical Identity

Molecular Formula

C12H14BrNO2

Molecular Weight

284.15 g/mol

Exact Mass

283.02079

PubChem CID

49786989

IUPAC Name

benzyl N-[(2R)-1-bromobut-3-en-2-yl]carbamate

SMILES String

C=C[C@H](CBr)NC(=O)OCc1ccccc1

Names & Synonyms

benzylN-[(2R)-1-bromobut-3-en-2-yl]carbamate
External Identifiers
EN300-319016

Catalog Overview

This compound is a chiral benzyl carbamate derivative containing both a bromine atom and a terminal alkene functionality. Its specific stereochemistry (R-configuration) and reactive groups make it a valuable intermediate in complex organic synthesis, particularly for constructing molecules with defined stereocenters and for further functionalization via halogen-based reactions or alkene transformations. It is intended for research and development applications.

Use Context

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

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

white solid

Physical State

solid

Melting Point

45.0 °C

Boiling Point

310.0 °C

Density

1.35 g/cm³

Water Solubility

very slightly soluble

Flash Point

160.0 °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 (PPE), including chemical-resistant gloves, safety goggles, and a lab coat. Work in a well-ventilated fume hood to avoid inhalation. Prevent skin and eye contact, and do not ingest. Always consult the Safety Data Sheet (SDS) for comprehensive hazard information and safe handling protocols before use.

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