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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)

(R)-(2-Iodo-1-methyl-ethyl)-carbamic acid tert-butyl ester, 95%CAS 446060-78-2
Tert-butyl (1-iodopropan-2-yl)carbamateCAS 363599-44-4
(S)-(2-Iodo-1-methyl-ethyl)-carbamic acid tert-butyl esterCAS 161529-20-0
tert-butyl N-(2-iodoethyl)-N-methylcarbamateCAS 918642-21-4
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.