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tert-butyl N-((2R)-4-bromobutan-2-yl)carbamate

CAS 106622-19-9Formula C9H18BrNO2MW 252.15PubChem 60087922

tert-butyl N-((2R)-4-bromobutan-2-yl)carbamate is a chiral bromo-substituted carbamate, commonly employed as a versatile building block in asymmetric synthesis for the preparation of complex organic molecules and pharmaceutical intermediates for research purposes.

Loading RDKit molecule structure...
InChIKey: BLROSIRAEKEFNI-SSDOTTSWSA-NC9H18BrNO2 | MW 252.15

Chemical Identity

Molecular Formula

C9H18BrNO2

Molecular Weight

252.15 g/mol

Exact Mass

251.05209

PubChem CID

60087922

IUPAC Name

tert-butyl N-[(2R)-4-bromobutan-2-yl]carbamate

SMILES String

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

Names & Synonyms

997-482-6tert-butylN-[(2R)-4-bromobutan-2-yl]carbamatetert-Butyl (R)-(4-bromobutan-2-yl)carbamate(R)-tert-Butyl (4-bromobutan-2-yl)carbamateG39222
External Identifiers
RefChem:894897SCHEMBL16706955CS-0376290EN300-23915716

Catalog Overview

tert-butyl N-((2R)-4-bromobutan-2-yl)carbamate, identified by CAS 106622-19-9, is an enantiomerically pure organic compound featuring a tert-butyl carbamate protecting group and a bromo-substituted butane chain with (2R) stereochemistry. With a molecular formula of C9H18BrNO2 and a molecular weight of 252.15, this compound serves as a crucial chiral intermediate. Its structure allows for selective functionalization at the bromine position, while the carbamate group provides amine protection, making it valuable in multi-step synthetic routes, particularly in the development of chiral pharmaceuticals and fine chemicals for research...

Use Context

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

tert-butyl N-((2R)-4-bromobutan-2-yl)carbamate, identified by CAS 106622-19-9, is an enantiomerically pure organic compound featuring a tert-butyl carbamate protecting group and a bromo-substituted butane chain with (2R) stereochemistry. With a molecular formula of C9H18BrNO2 and a molecular weight of 252.15, this compound serves as a crucial chiral intermediate. Its structure allows for selective functionalization at the bromine position, while the carbamate group provides amine protection, making it valuable in multi-step synthetic routes, particularly in the development of chiral pharmaceuticals and fine chemicals for research use.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

colorless liquid

Physical State

liquid

Melting Point

-5.0 °C

Boiling Point

260.0 °C

Density

1.25 g/cm³

Water Solubility

sparingly soluble

Flash Point

120.0 °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 tert-butyl N-((2R)-4-bromobutan-2-yl)carbamate in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including chemical-resistant gloves, eye protection, and a lab coat. Avoid inhalation of dust or vapors, ingestion, and direct skin or eye contact. Store in a cool, dry place, away from incompatible materials. Always consult the Safety Data Sheet (SDS) for comprehensive safety information and handling procedures before use in a research setting.

Related Products / Graph Discovery

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

Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 292429GHS Pictograms: GHS07, GHS09Shipment 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.