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tert-butyl N-(1-bromo-3-methylbutan-2-yl)carbamate

CAS 317385-11-8Formula C10H20BrNO2MW 266.18PubChem 14427207

tert-butyl N-(1-bromo-3-methylbutan-2-yl)carbamate is a functionalized intermediate with the chemical formula C10H20BrNO2. This compound features a tert-butyl carbamate (Boc) protecting group and a bromine atom, making it a versatile building block for various organic synthesis applications.

Loading RDKit molecule structure...
InChIKey: MGTUVIJGSSSBTN-UHFFFAOYSA-NC10H20BrNO2 | MW 266.18

Chemical Identity

Molecular Formula

C10H20BrNO2

Molecular Weight

266.18 g/mol

Exact Mass

265.06774

PubChem CID

14427207

SMILES String

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

Names & Synonyms

875-036-0tert-Butyl (1-bromo-3-methylbutan-2-yl)carbamate
External Identifiers
RefChem:895340starbld0027747EN300-1881376

Catalog Overview

tert-butyl N-(1-bromo-3-methylbutan-2-yl)carbamate, with CAS 317385-11-8, is a key research-use chemical intermediate. It incorporates a Boc-protected amine and a bromo-substituted alkyl chain, providing dual functionality for synthetic chemists. The Boc group offers robust protection for the amine during multi-step syntheses, while the bromine atom serves as a reactive site for further transformations, including nucleophilic substitutions, cross-coupling reactions, and the formation of organometallic reagents. Its structure makes it particularly useful in the construction of complex organic molecules, including potential...

Use Context

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

tert-butyl N-(1-bromo-3-methylbutan-2-yl)carbamate, with CAS 317385-11-8, is a key research-use chemical intermediate. It incorporates a Boc-protected amine and a bromo-substituted alkyl chain, providing dual functionality for synthetic chemists. The Boc group offers robust protection for the amine during multi-step syntheses, while the bromine atom serves as a reactive site for further transformations, including nucleophilic substitutions, cross-coupling reactions, and the formation of organometallic reagents. Its structure makes it particularly useful in the construction of complex organic molecules, including potential pharmaceutical intermediates and specialty chemicals.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

white crystalline solid

Physical State

solid

Melting Point

38.3 °C

Boiling Point

265.3 °C

Density

1.18 g/cm³

Water Solubility

1.38 × 10⁻³ mol/L

Flash Point

126.6 °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. Store in a cool, dry place, away from incompatible materials. Dispose of according to local regulations for chemical waste.

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.