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Tert-butyl (1-bromo-4-methylpentan-2-yl)carbamate

CAS 142121-32-2Formula C11H22BrNO2MW 280.2PubChem 19107596

Tert-butyl (1-bromo-4-methylpentan-2-yl)carbamate is a bromo-substituted carbamate derivative, commonly employed as a functionalized intermediate in organic synthesis. It features a tert-butyl carbamate (Boc) protecting group and a bromine atom, making it suitable for various coupling reactions and the introduction of protected amino functionalities in research applications.

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

Chemical Identity

Molecular Formula

C11H22BrNO2

Molecular Weight

280.2 g/mol

Exact Mass

279.08339

PubChem CID

19107596

IUPAC Name

tert-butyl N-(1-bromo-4-methylpentan-2-yl)carbamate

SMILES String

CC(C)CC(CBr)NC(=O)OC(C)(C)C

Names & Synonyms

QOUMJXYJNQUGAT-UHFFFAOYSA-Ntert-butyl(1-bromo-4-methylpentan-2-yl)carbamateN-tert-butoxycarbonyl-1-bromo-2-amino-4-methylpentane
External Identifiers
SCHEMBL8560322SFA12132EN300-366884

Catalog Overview

Tert-butyl (1-bromo-4-methylpentan-2-yl)carbamate, with CAS 142121-32-2 and molecular formula C11H22BrNO2, is a key functionalized intermediate in synthetic organic chemistry. This compound incorporates a tert-butyl carbamate (Boc) group, which serves as a robust protecting group for the amine functionality, alongside a reactive bromine atom. The presence of both a protected amine and a halogen makes it a versatile building block for constructing complex molecules. Researchers utilize this compound in various synthetic pathways, including nucleophilic substitution reactions, cross-coupling reactions (e.

Use Context

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

Tert-butyl (1-bromo-4-methylpentan-2-yl)carbamate, with CAS 142121-32-2 and molecular formula C11H22BrNO2, is a key functionalized intermediate in synthetic organic chemistry. This compound incorporates a tert-butyl carbamate (Boc) group, which serves as a robust protecting group for the amine functionality, alongside a reactive bromine atom. The presence of both a protected amine and a halogen makes it a versatile building block for constructing complex molecules. Researchers utilize this compound in various synthetic pathways, including nucleophilic substitution reactions, cross-coupling reactions (e.g., Suzuki, Heck, Sonogashira after conversion to an organometallic species), and as a precursor for further derivatization. Its structure, featuring an isobutyl side chain, allows for the introduction of specific steric and electronic properties into target compounds. It is intended for research use only.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

Colorless liquid

Physical State

Liquid

Melting Point

5.0 °C

Boiling Point

300.0 °C

Density

1.25 g/cm³

Water Solubility

Insoluble

Flash Point

150.0 °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 immediately with plenty of water. Store in a cool, dry place, away from incompatible materials. Refer to 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)

tert-butyl N-(3-bromopropyl)-N-(propan-2-yl)carbamateCAS 1525991-29-0
tert-butyl N-(5-bromopentyl)-N-methylcarbamateCAS 1694011-13-6
tert-butyl N-(5-bromo-2-methylpentan-2-yl)carbamateCAS 2354094-36-1
tert-butyl N-(6-bromohexan-2-yl)carbamateCAS 1936119-40-2
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: GHS07Shipment review: Shipment details require review before fulfillment.

Compliance cues are non-linked reference tags and require shipment review.