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tert-butyl N-(3-bromo-2-methylpropyl)carbamate

CAS 1510268-47-9Formula C9H18BrNO2MW 252.15PubChem 86039219

tert-butyl N-(3-bromo-2-methylpropyl)carbamate is a bromo-substituted carbamate derivative, primarily utilized as a functionalized intermediate in organic synthesis. Its structure features a tert-butyl carbamate protecting group and a bromomethyl group, making it valuable for introducing protected amine functionalities and subsequent halogen-based reactions in research applications.

Loading RDKit molecule structure...
InChIKey: HYTMOLGBQNHTPA-UHFFFAOYSA-NC9H18BrNO2 | MW 252.15

Chemical Identity

Molecular Formula

C9H18BrNO2

Molecular Weight

252.15 g/mol

Exact Mass

251.05209

PubChem CID

86039219

SMILES String

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

Names & Synonyms

843-885-6tert-Butyl (3-bromo-2-methylpropyl)carbamate1-(Boc-amino)-3-bromo-2-methylpropanetert-Butyl(3-bromo-2-methylpropyl)carbamateI10772
Show all synonyms
tert-butyl N-(3-bromo-2-methyl-propyl)carbamate
External Identifiers
RefChem:895933MFCD24168790SCHEMBL6518304KKC26847EN300-1882968

Catalog Overview

tert-butyl N-(3-bromo-2-methylpropyl)carbamate, with CAS 1510268-47-9 and molecular formula C9H18BrNO2, is a synthetic organic compound characterized by a tert-butyl carbamate group attached to a 3-bromo-2-methylpropyl chain. This compound serves as a versatile building block in chemical synthesis, particularly for the introduction of protected primary amine groups and subsequent transformations involving the bromine atom. The carbamate group offers protection for the amine functionality, which can be deprotected under acidic conditions to yield the free amine. The bromine atom provides a reactive site for various coupling...

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Read more catalog context

tert-butyl N-(3-bromo-2-methylpropyl)carbamate, with CAS 1510268-47-9 and molecular formula C9H18BrNO2, is a synthetic organic compound characterized by a tert-butyl carbamate group attached to a 3-bromo-2-methylpropyl chain. This compound serves as a versatile building block in chemical synthesis, particularly for the introduction of protected primary amine groups and subsequent transformations involving the bromine atom. The carbamate group offers protection for the amine functionality, which can be deprotected under acidic conditions to yield the free amine. The bromine atom provides a reactive site for various coupling reactions, nucleophilic substitutions, or Grignard reactions, enabling the construction of more complex molecular architectures. It is a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals for research purposes.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

white solid

Physical State

solid

Melting Point

30.5 °C

Boiling Point

260.6 °C

Density

1.22 g/cm³

Water Solubility

3.39 × 10⁻³ mol/L

Flash Point

120.1 °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 under a 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. Consult the Safety Data Sheet (SDS) for detailed hazard information and emergency procedures. This product is for research use only and not for human or animal therapeutic or diagnostic use.

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