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tert-butyl N-(5-bromopentyl)-N-methylcarbamate

CAS 1694011-13-6Formula C11H22BrNO2MW 280.2PubChem 107206130

tert-butyl N-(5-bromopentyl)-N-methylcarbamate is a functionalized intermediate featuring a protected N-methylamine and a terminal bromo group on a pentyl chain. It is primarily used in organic synthesis as a versatile building block for creating more complex molecules for research purposes.

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

Chemical Identity

Molecular Formula

C11H22BrNO2

Molecular Weight

280.2 g/mol

Exact Mass

279.08339

PubChem CID

107206130

SMILES String

CN(CCCCCBr)C(=O)OC(C)(C)C

Names & Synonyms

878-342-2TERT-BUTYL (5-BROMOPENTYL)(METHYL)CARBAMATEtert-butylN-(5-bromopentyl)-N-methylcarbamatetert-butyl N-(5-bromopentyl)-N-methyl-carbamate
External Identifiers
RefChem:896234SCHEMBL19635933AT11153DB-419077CS-0530012EN300-7160657

Catalog Overview

tert-butyl N-(5-bromopentyl)-N-methylcarbamate, identified by CAS 1694011-13-6, is an organic compound with the molecular formula C11H22BrNO2 and a molecular weight of 280. 20 g/mol. This molecule incorporates a tert-butyl carbamate (Boc) protecting group on an N-methylamine, attached to a 5-bromopentyl chain. The presence of both a protected amine and a reactive alkyl bromide makes it a valuable intermediate in multi-step organic synthesis.

Use Context

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

tert-butyl N-(5-bromopentyl)-N-methylcarbamate, identified by CAS 1694011-13-6, is an organic compound with the molecular formula C11H22BrNO2 and a molecular weight of 280.20 g/mol. This molecule incorporates a tert-butyl carbamate (Boc) protecting group on an N-methylamine, attached to a 5-bromopentyl chain. The presence of both a protected amine and a reactive alkyl bromide makes it a valuable intermediate in multi-step organic synthesis. It can be utilized in various coupling reactions, nucleophilic substitutions, and as a precursor for synthesizing diverse nitrogen-containing compounds, particularly in pharmaceutical and agrochemical research.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

colorless

Physical State

liquid

Melting Point

23.4 °C

Boiling Point

307.0 °C

Density

1.18 g/cm³

Water Solubility

2.18 × 10⁻³ mol/L

Flash Point

127.0 °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
  • When handling tert-butyl N-(5-bromopentyl)-N-methylcarbamate, researchers should adhere to standard laboratory safety practices. This includes wearing appropriate personal protective equipment such as gloves, eye protection, and a lab coat. Work in a well-ventilated area or under a fume hood to avoid inhalation. Avoid contact with skin and eyes. In case of contact, rinse thoroughly with water. Store the compound in a cool, dry place, away from incompatible materials. 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: 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.