MolGraphChemical Intelligence
Active Chemical RecordCatalog PreviewCatalog ready

(S)-(2-Iodo-1-methyl-ethyl)-carbamic acid benzyl ester

CAS 136464-11-4Formula C11H14INO2MW 319.14PubChem 11056266

This compound is a chiral benzyl carbamate derivative containing an iodine atom, primarily used as a functionalized intermediate in organic synthesis for research purposes.

Loading RDKit molecule structure...
InChIKey: NTUAECGJTISEEG-VIFPVBQESA-NC11H14INO2 | MW 319.14

Chemical Identity

Molecular Formula

C11H14INO2

Molecular Weight

319.14 g/mol

Exact Mass

319.00693

PubChem CID

11056266

IUPAC Name

benzyl N-[(2S)-1-iodopropan-2-yl]carbamate

SMILES String

C[C@@H](CI)NC(=O)OCc1ccccc1

Names & Synonyms

(S)-Benzyl (1-iodopropan-2-yl)carbamateC11H14INO2Carbamic acid, N-[(1S)-2-iodo-1-methylethyl]-, phenylmethyl esterbenzyl (S)-(1-iodopropan-2-yl)carbamate(S)-Benzyl(1-iodopropan-2-yl)carbamate
Show all synonyms
benzyl N-[(1S)-2-iodo-1-methyl-ethyl]carbamate
External Identifiers
MFCD26954722DB-258119CS-0340691

Catalog Overview

(S)-(2-Iodo-1-methyl-ethyl)-carbamic acid benzyl ester, also known as benzyl N-[(2S)-1-iodopropan-2-yl]carbamate, is an organoiodine compound featuring a carbamate protecting group and a chiral center. With a molecular formula of C11H14INO2 and a molecular weight of 319. 14, this compound serves as a versatile building block in the synthesis of complex organic molecules. Its iodine functionality allows for various coupling reactions and transformations, while the benzyl carbamate group provides amine protection that can be selectively removed.

Use Context

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

(S)-(2-Iodo-1-methyl-ethyl)-carbamic acid benzyl ester, also known as benzyl N-[(2S)-1-iodopropan-2-yl]carbamate, is an organoiodine compound featuring a carbamate protecting group and a chiral center. With a molecular formula of C11H14INO2 and a molecular weight of 319.14, this compound serves as a versatile building block in the synthesis of complex organic molecules. Its iodine functionality allows for various coupling reactions and transformations, while the benzyl carbamate group provides amine protection that can be selectively removed. It is particularly valuable in stereoselective synthesis due to its defined (S) configuration, making it useful in the preparation of chiral intermediates for pharmaceutical and fine chemical research.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White crystalline solid

Physical State

Solid

Melting Point

95.0 °C

Boiling Point

370.0 °C

Density

1.65 g/cm³

Water Solubility

Insoluble

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 with appropriate personal protective equipment (PPE) including gloves, eye protection, and a lab coat. Use in a well-ventilated area or fume hood to avoid inhalation. Avoid contact with skin and eyes. Store in a cool, dry place, away from incompatible materials. Dispose of waste in accordance with local regulations for research-use chemicals.

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.