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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

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  • 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.

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