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1-(Tert-butoxycarbonylamino)-2-iodopropane

CAS 220594-87-6Formula C8H16INO2MW 285.12PubChem 21194519

1-(Tert-butoxycarbonylamino)-2-iodopropane is a functionalized intermediate featuring a Boc-protected amine and an iodine atom. It is primarily used in organic synthesis as a versatile building block for introducing protected amino groups and for various coupling reactions or nucleophilic substitutions.

Loading RDKit molecule structure...
InChIKey: SKVKCUBQJWQTFG-UHFFFAOYSA-NC8H16INO2 | MW 285.12

Chemical Identity

Molecular Formula

C8H16INO2

Molecular Weight

285.12 g/mol

Exact Mass

285.02258

PubChem CID

21194519

IUPAC Name

tert-butyl N-(2-iodopropyl)carbamate

SMILES String

CC(I)CNC(=O)OC(C)(C)C

Names & Synonyms

H57225
External Identifiers
SCHEMBL7884773

Catalog Overview

1-(Tert-butoxycarbonylamino)-2-iodopropane, also known as tert-butyl N-(2-iodopropyl)carbamate, is an organoiodine compound with the molecular formula C8H16INO2. This chemical is characterized by a tert-butoxycarbonyl (Boc) protecting group on an amine, and an iodine atom attached to the second carbon of a propyl chain. Its structure makes it a valuable intermediate in complex organic synthesis, enabling the introduction of a protected primary amine functionality while the iodine atom serves as a reactive site for further chemical transformations, such as cross-coupling reactions (e. g.

Use Context

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

1-(Tert-butoxycarbonylamino)-2-iodopropane, also known as tert-butyl N-(2-iodopropyl)carbamate, is an organoiodine compound with the molecular formula C8H16INO2. This chemical is characterized by a tert-butoxycarbonyl (Boc) protecting group on an amine, and an iodine atom attached to the second carbon of a propyl chain. Its structure makes it a valuable intermediate in complex organic synthesis, enabling the introduction of a protected primary amine functionality while the iodine atom serves as a reactive site for further chemical transformations, such as cross-coupling reactions (e.g., Suzuki, Heck) or nucleophilic displacement reactions.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White crystalline solid

Physical State

Solid

Melting Point

85.0 °C

Boiling Point

280.0 °C

Density

1.65 g/cm³

Water Solubility

Slightly soluble

Flash Point

180.0 °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 1-(Tert-butoxycarbonylamino)-2-iodopropane 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. Store in a cool, dry place, away from incompatible materials. 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.

Similar products (text references)

1909325-77-4CAS 1909325-77-4

Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 292419GHS 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.