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(R)-tert-butyl 1-bromopropan-2-ylcarbamate

CAS 263410-22-6Formula C8H16BrNO2MW 238.12PubChem 57081792

(R)-tert-butyl 1-bromopropan-2-ylcarbamate is a chiral brominated carbamate derivative, primarily used as a versatile building block or intermediate in organic synthesis for research purposes, particularly in the preparation of stereochemically defined compounds.

Loading RDKit molecule structure...
InChIKey: OTOODTHBNJYOIV-ZCFIWIBFSA-NC8H16BrNO2 | MW 238.12

Chemical Identity

Molecular Formula

C8H16BrNO2

Molecular Weight

238.12 g/mol

Exact Mass

237.03644

PubChem CID

57081792

IUPAC Name

tert-butyl N-[(2R)-1-bromopropan-2-yl]carbamate

SMILES String

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

Names & Synonyms

tert-butyl (R)-(1-bromopropan-2-yl)carbamateC8H16BrNO2OTOODTHBNJYOIV-ZCFIWIBFSA-Nt-Butyl (R)-(1-bromopropan-2-yl)carbamate
External Identifiers
SCHEMBL2065190MFCD18373976AT39312

Catalog Overview

(R)-tert-butyl 1-bromopropan-2-ylcarbamate, identified by CAS 263410-22-6, is a chiral brominated carbamate. This compound serves as a versatile functionalized intermediate in synthetic organic chemistry, particularly in the preparation of stereochemically defined compounds. Its structure incorporates a tert-butyl carbamate (Boc) protecting group on an amine, and a bromine atom on the adjacent carbon of a propyl chain, with an (R) configuration at the chiral center. Researchers utilize this compound for its reactivity in nucleophilic substitution reactions, enabling the introduction of various functionalities while maintaining or...

Use Context

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

(R)-tert-butyl 1-bromopropan-2-ylcarbamate, identified by CAS 263410-22-6, is a chiral brominated carbamate. This compound serves as a versatile functionalized intermediate in synthetic organic chemistry, particularly in the preparation of stereochemically defined compounds. Its structure incorporates a tert-butyl carbamate (Boc) protecting group on an amine, and a bromine atom on the adjacent carbon of a propyl chain, with an (R) configuration at the chiral center. Researchers utilize this compound for its reactivity in nucleophilic substitution reactions, enabling the introduction of various functionalities while maintaining or inverting stereochemistry, making it valuable in the synthesis of complex molecules and pharmaceutical intermediates for research purposes.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

colorless liquid

Physical State

liquid

Melting Point

10.0 °C

Boiling Point

220.0 °C

Density

1.3 g/cm³

Water Solubility

sparingly soluble

Flash Point

100.0 °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, 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 thoroughly with water. Store in a cool, dry place, away from incompatible materials. Consult the Safety Data Sheet (SDS) for comprehensive safety information.

Related Products / Graph Discovery

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

Similar products (text references)

2679839-22-4CAS 2679839-22-4

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.