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(2-Bromoethyl)-ethylcarbamic acid tert-butyl ester

CAS 1508841-86-8Formula C9H18BrNO2MW 252.15PubChem 114293381

tert-Butyl N-(2-bromoethyl)-N-ethylcarbamate is a functionalized intermediate featuring a bromoethyl group and a tert-butyl protected ethylcarbamate. It is primarily utilized in organic synthesis as a versatile building block for introducing ethylamino functionalities or for further derivatization via the reactive bromoethyl moiety.

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

Chemical Identity

Molecular Formula

C9H18BrNO2

Molecular Weight

252.15 g/mol

Exact Mass

251.05209

PubChem CID

114293381

IUPAC Name

tert-butyl N-(2-bromoethyl)-N-ethylcarbamate

SMILES String

CCN(CCBr)C(=O)OC(C)(C)C

Names & Synonyms

(2-Bromo-ethyl)-ethyl-carbamic acid tert-butyl estertert-Butyl (2-bromoethyl)(ethyl)carbamateA1-03363
External Identifiers
EN300-4327645

Catalog Overview

tert-Butyl N-(2-bromoethyl)-N-ethylcarbamate, also known as (2-Bromoethyl)-ethylcarbamic acid tert-butyl ester, is an organic compound with the molecular formula C9H18BrNO2 and a molecular weight of 252. 15 g/mol. This compound combines a reactive bromoethyl group with an N-ethylcarbamate protected by a tert-butyl group. The bromoethyl functionality serves as an electrophilic site, enabling reactions such as nucleophilic substitutions to form new carbon-heteroatom or carbon-carbon bonds.

Use Context

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

tert-Butyl N-(2-bromoethyl)-N-ethylcarbamate, also known as (2-Bromoethyl)-ethylcarbamic acid tert-butyl ester, is an organic compound with the molecular formula C9H18BrNO2 and a molecular weight of 252.15 g/mol. This compound combines a reactive bromoethyl group with an N-ethylcarbamate protected by a tert-butyl group. The bromoethyl functionality serves as an electrophilic site, enabling reactions such as nucleophilic substitutions to form new carbon-heteroatom or carbon-carbon bonds. The tert-butyl carbamate (Boc) group acts as a common protecting group for the nitrogen atom, which can be selectively deprotected under acidic conditions to reveal a secondary amine. This makes it a valuable intermediate in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, where controlled introduction of ethylamino groups and subsequent functionalization are required.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

Colorless liquid

Physical State

Liquid

Melting Point

-30.0 °C

Boiling Point

220.0 °C

Density

1.25 g/cm³

Water Solubility

Insoluble

Flash Point

100.0 °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 tert-Butyl N-(2-bromoethyl)-N-ethylcarbamate in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Avoid inhalation of dust or vapors, and prevent skin and eye contact. 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 detailed 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: 290399GHS Pictograms: GHS07, GHS09Shipment 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.