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5-(Iodomethyl)-4,4-dimethyl-1,3-oxazolidin-2-one

CAS 2490431-95-1Formula C6H10INO2MW 255.05PubChem 155820934

5-(Iodomethyl)-4,4-dimethyl-1,3-oxazolidin-2-one is a functionalized oxazolidinone derivative containing an iodomethyl group. This compound is primarily intended for research and development applications as a versatile synthetic intermediate.

Loading RDKit molecule structure...
InChIKey: HGZYOLPFTFXZSD-UHFFFAOYSA-NC6H10INO2 | MW 255.05

Chemical Identity

Molecular Formula

C6H10INO2

Molecular Weight

255.05 g/mol

Exact Mass

254.97563

PubChem CID

155820934

SMILES String

CC1(C)NC(=O)OC1CI

Names & Synonyms

102-312-3
External Identifiers
RefChem:531315EN300-27113149

Catalog Overview

5-(Iodomethyl)-4,4-dimethyl-1,3-oxazolidin-2-one, with CAS 2490431-95-1 and molecular formula C6H10INO2, is a heterocyclic organic compound featuring a 1,3-oxazolidin-2-one core substituted with two methyl groups and an iodomethyl moiety. The iodomethyl group serves as a reactive site, making this compound a valuable building block in organic synthesis. It can be utilized in various chemical transformations, including nucleophilic substitution reactions, palladium-catalyzed cross-coupling reactions, or as a precursor for further functionalization. Its oxazolidinone structure may also lend itself to applications involving chiral...

Use Context

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

5-(Iodomethyl)-4,4-dimethyl-1,3-oxazolidin-2-one, with CAS 2490431-95-1 and molecular formula C6H10INO2, is a heterocyclic organic compound featuring a 1,3-oxazolidin-2-one core substituted with two methyl groups and an iodomethyl moiety. The iodomethyl group serves as a reactive site, making this compound a valuable building block in organic synthesis. It can be utilized in various chemical transformations, including nucleophilic substitution reactions, palladium-catalyzed cross-coupling reactions, or as a precursor for further functionalization. Its oxazolidinone structure may also lend itself to applications involving chiral auxiliaries or as a scaffold in medicinal chemistry research, though specific chiral information is not provided. This chemical is for research use only.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White crystalline powder

Physical State

Solid

Melting Point

95.0 °C

Boiling Point

280.0 °C

Density

1.75 g/cm³

Water Solubility

Slightly soluble

Flash Point

165.0 °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 5-(Iodomethyl)-4,4-dimethyl-1,3-oxazolidin-2-one in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Avoid inhalation, ingestion, and skin contact. Refer to the Safety Data Sheet (SDS) for comprehensive safety information and emergency procedures. Store in a cool, dry place, away from incompatible materials.

Related Products / Graph Discovery

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

Similar products (text references)

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Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 293499GHS 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.