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tert-butyl N-(3-bromopropyl)-N-(propan-2-yl)carbamate

CAS 1525991-29-0Formula C11H22BrNO2MW 280.2PubChem 53807172

This compound is a functionalized intermediate, specifically a tert-butyl carbamate derivative containing a bromopropyl group and an isopropyl group. It is primarily used in organic synthesis as a building block for creating more complex molecules, particularly in pharmaceutical research and fine chemical development.

Loading RDKit molecule structure...
InChIKey: FMNMFUAKDFDIMP-UHFFFAOYSA-NC11H22BrNO2 | MW 280.2

Chemical Identity

Molecular Formula

C11H22BrNO2

Molecular Weight

280.2 g/mol

Exact Mass

279.08339

PubChem CID

53807172

IUPAC Name

tert-butyl N-(3-bromopropyl)-N-propan-2-ylcarbamate

SMILES String

CC(C)N(CCCBr)C(=O)OC(C)(C)C

Names & Synonyms

tert-butylN-(3-bromopropyl)-N-(propan-2-yl)carbamate
External Identifiers
SCHEMBL8328107EN300-174600

Catalog Overview

tert-butyl N-(3-bromopropyl)-N-(propan-2-yl)carbamate, identified by CAS 1525991-29-0, is an organic compound with the molecular formula C11H22BrNO2 and a molecular weight of 280. 20 g/mol. It features a tert-butyl carbamate protecting group on a nitrogen atom, which is also substituted with an isopropyl group and a 3-bromopropyl chain. This structure makes it a versatile functionalized intermediate in synthetic chemistry.

Use Context

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

tert-butyl N-(3-bromopropyl)-N-(propan-2-yl)carbamate, identified by CAS 1525991-29-0, is an organic compound with the molecular formula C11H22BrNO2 and a molecular weight of 280.20 g/mol. It features a tert-butyl carbamate protecting group on a nitrogen atom, which is also substituted with an isopropyl group and a 3-bromopropyl chain. This structure makes it a versatile functionalized intermediate in synthetic chemistry. The bromo-group serves as a reactive site for various coupling reactions, nucleophilic substitutions, or further functionalization, while the carbamate group can be selectively deprotected to yield a secondary amine. Its utility lies in the construction of diverse chemical scaffolds, particularly in the synthesis of nitrogen-containing heterocycles and complex organic molecules for research purposes.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

colorless to pale yellow liquid

Physical State

liquid

Melting Point

-10.0 °C

Boiling Point

250.0 °C

Density

1.1 g/cm³

Water Solubility

insoluble

Flash Point

115.0 °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-(3-bromopropyl)-N-(propan-2-yl)carbamate in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including safety goggles, chemical-resistant gloves (e.g., nitrile), and a lab coat. Avoid inhalation of dust or vapors, and prevent skin and eye contact. In case of contact, rinse immediately with plenty of water. Store in a cool, dry place, away from incompatible materials. Always consult the Safety Data Sheet (SDS) for comprehensive safety information before use.

Related Products / Graph Discovery

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

Similar products (text references)

1566794-10-2CAS 1566794-10-2

Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 29241990GHS 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.