Active Chemical RecordCatalog PreviewCatalog ready

Methyl 3-(chloromethyl)-1-ethylazetidine-3-carboxylate

CAS 2225154-16-3Formula C8H14ClNO2MW 191.65PubChem 137964014

Methyl 3-(chloromethyl)-1-ethylazetidine-3-carboxylate is a chlorinated azetidine derivative featuring a methyl ester group. This compound is primarily intended for research and development purposes as a versatile building block in organic synthesis. Its unique structural features make it suitable for various chemical transformations, particularly in the creation of novel heterocyclic compounds.

Loading RDKit molecule structure...
InChIKey: CPJZJZCUFZBYNG-UHFFFAOYSA-NC8H14ClNO2 | MW 191.65

Chemical Identity

Molecular Formula

C8H14ClNO2

Molecular Weight

191.65 g/mol

Exact Mass

191.071306

PubChem CID

137964014

SMILES String

CCN1CC(CCl)(C(=O)OC)C1

Names & Synonyms

995-802-9
External Identifiers
RefChem:814978starbld0041418EN300-1717126

Catalog Overview

Methyl 3-(chloromethyl)-1-ethylazetidine-3-carboxylate, with CAS number 2225154-16-3 and molecular formula C8H14ClNO2, is a synthetic organic compound characterized by an azetidine ring system. The azetidine nitrogen is substituted with an ethyl group, while the C3 position bears both a chloromethyl group and a methyl ester functionality. This combination of functional groups provides multiple reactive sites, making it a valuable intermediate in complex organic synthesis. It can undergo reactions such as nucleophilic substitutions at the chloromethyl group, ester hydrolysis or transesterification, and modifications of the...

Use Context

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

Methyl 3-(chloromethyl)-1-ethylazetidine-3-carboxylate, with CAS number 2225154-16-3 and molecular formula C8H14ClNO2, is a synthetic organic compound characterized by an azetidine ring system. The azetidine nitrogen is substituted with an ethyl group, while the C3 position bears both a chloromethyl group and a methyl ester functionality. This combination of functional groups provides multiple reactive sites, making it a valuable intermediate in complex organic synthesis. It can undergo reactions such as nucleophilic substitutions at the chloromethyl group, ester hydrolysis or transesterification, and modifications of the azetidine ring. Researchers may utilize this compound for the synthesis of pharmaceuticals, agrochemicals, or advanced materials, leveraging its azetidine core and reactive side chains. It is supplied for Research Use Only (RUO).

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

colorless liquid

Physical State

liquid

Melting Point

-10.0 °C

Boiling Point

220.0 °C

Density

1.15 g/cm³

Water Solubility

slightly soluble

Flash Point

95.0 °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 Methyl 3-(chloromethyl)-1-ethylazetidine-3-carboxylate in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including safety goggles, gloves, and a lab coat, to prevent skin and eye contact. Avoid inhalation of dust or vapors. 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 handling. This product is for Research Use Only and not for human or animal therapeutic or diagnostic use.

Related Products / Graph Discovery

Related products, derivatives, keywords, and application cues for catalog discovery.

Related products and analog discovery will be available as catalog graph data is expanded.