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tert-butyl N-[(3R)-1-bromo-5-methylhexan-3-yl]carbamate

CAS 2624109-36-8Formula C12H24BrNO2MW 294.23PubChem 155977814

This compound is a bromo-substituted carbamate derivative, specifically a tert-butyl N-[(3R)-1-bromo-5-methylhexan-3-yl]carbamate. It features a chiral center at the 3-position with an (R) configuration, a bromoethyl group, and an isobutyl moiety, making it a versatile building block in organic synthesis.

Loading RDKit molecule structure...
InChIKey: HMZNTBNNUXWKAV-JTQLQIEISA-NC12H24BrNO2 | MW 294.23

Chemical Identity

Molecular Formula

C12H24BrNO2

Molecular Weight

294.23 g/mol

Exact Mass

293.09904

PubChem CID

155977814

SMILES String

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

Names & Synonyms

tert-butyl N-((3R)-1-bromo-5-methylhexan-3-yl)carbamate973-638-9
External Identifiers
RefChem:895011EN300-27748681

Catalog Overview

tert-butyl N-[(3R)-1-bromo-5-methylhexan-3-yl]carbamate, identified by CAS 2624109-36-8, is a chiral organic compound with the molecular formula C12H24BrNO2 and a molecular weight of 294. 23 g/mol. It incorporates a tert-butyl carbamate protecting group on a secondary amine, a bromo-substituted alkyl chain, and an isobutyl group. The presence of the bromine atom provides a reactive site for various synthetic transformations, such as nucleophilic substitutions or cross-coupling reactions.

Use Context

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

tert-butyl N-[(3R)-1-bromo-5-methylhexan-3-yl]carbamate, identified by CAS 2624109-36-8, is a chiral organic compound with the molecular formula C12H24BrNO2 and a molecular weight of 294.23 g/mol. It incorporates a tert-butyl carbamate protecting group on a secondary amine, a bromo-substituted alkyl chain, and an isobutyl group. The presence of the bromine atom provides a reactive site for various synthetic transformations, such as nucleophilic substitutions or cross-coupling reactions. The (3R) stereochemistry is crucial for applications requiring specific enantiomeric purity. This compound is classified as a functionalized intermediate, suitable for advanced synthetic routes in medicinal chemistry and materials science.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

Colorless liquid

Physical State

Liquid

Melting Point

-5.0 °C

Boiling Point

305.0 °C

Density

1.25 g/cm³

Water Solubility

Very slightly soluble

Flash Point

170.0 °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-[(3R)-1-bromo-5-methylhexan-3-yl]carbamate in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including gloves, eye protection, and a lab coat, to prevent skin and eye contact. Avoid inhalation of dust or vapors. 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 detailed hazard information and safe handling procedures. This product is for research use only and not for human or animal therapeutic or diagnostic use.

Related Products / Graph Discovery

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

Similar products (text references)

170876-68-3CAS 170876-68-3
2836923-84-1CAS 2836923-84-1

Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 290349GHS 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.