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(3-Bromo-1-methylpropyl)carbamic acid tert-butyl ester

CAS 128412-15-7Formula C9H18BrNO2MW 252.15PubChem 72345830

tert-Butyl N-(4-bromobutan-2-yl)carbamate is a functionalized intermediate featuring a tert-butyl carbamate protecting group and a reactive bromine atom. It is primarily used as a versatile building block in organic synthesis.

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

Chemical Identity

Molecular Formula

C9H18BrNO2

Molecular Weight

252.15 g/mol

Exact Mass

251.05209

PubChem CID

72345830

IUPAC Name

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

SMILES String

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

Names & Synonyms

tert-Butyl (4-bromobutan-2-yl)carbamate2-(Boc-amino)-4-bromobutanetert-Butyl(4-bromobutan-2-yl)carbamateI10925tert-butyl N-(3-bromo-1-methyl-propyl)carbamate
Show all synonyms
F501472
External Identifiers
MFCD22576327SCHEMBL4745621AKOS027251209AS-49494SY244626DB-309865CS-0045328

Catalog Overview

tert-Butyl N-(4-bromobutan-2-yl)carbamate is an organic compound characterized by a tert-butyl carbamate (Boc) protecting group and a bromine atom on a four-carbon chain. The Boc group serves to protect an amine functionality, while the bromine atom acts as a reactive site for various synthetic transformations. This compound is classified as a functionalized intermediate, making it valuable in multi-step organic synthesis.

Use Context

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

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

Colorless liquid

Physical State

Liquid

Melting Point

15.0 °C

Boiling Point

270.0 °C

Density

1.25 g/cm³

Water Solubility

Slightly 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 with appropriate personal protective equipment, including chemical-resistant gloves, safety glasses, and a lab coat. Use in a well-ventilated area or a fume hood to prevent 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. 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.

Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 292419GHS 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.