58879-36-0

Basic information

• Product Name: 2(3H)-Furanone, dihydro-5-(iodomethyl)-, (5S)-
• CAS NO: 58879-36-0
• Molecular Formula: C5H7IO2
• Molecular Weight: 226.014
• Mol File: 58879-36-0.mol

Chemical Properties

• CAS DataBase Reference: 2(3H)-Furanone, dihydro-5-(iodomethyl)-, (5S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Furanone, dihydro-5-(iodomethyl)-, (5S)-(58879-36-0)
• EPA Substance Registry System: 2(3H)-Furanone, dihydro-5-(iodomethyl)-, (5S)-(58879-36-0)

Safety Data

• Hazardous Substances Data: 58879-36-0(Hazardous Substances Data)

Usage

Type of compound

Synthetic organic compound

Common uses

Intermediate in the production of pharmaceuticals and other organic compounds

Derivative

Dihydro-derivative of 2(3H)-furanone

Contains

Iodomethyl group

Predominant use

Organic synthesis and as a building block for the creation of various pharmaceuticals and fine chemicals

Reactivity

Versatile

Safety

Handle with care and follow safety protocols to avoid health and safety risks.

Upstream product

• 32780-06-6 (5S)-5-(hydroxymethyl)-2-oxo-tetrahydrofuran 

Downstream Products

• 138298-25-6 (+)-(R)-5-(3-phenylpropyl)dihydrofuran-2(3H)-one 
• 110793-80-1 (R)-5-But-3-enyl-dihydro-furan-2-one 
• 134133-76-9 (S)-5-[(2R,6S,11R)-8-(tert-Butyl-dimethyl-silanyloxy)-6,11-dimethyl-1,2,5,6-tetrahydro-4H-2,6-methano-benzo[d]azocin-3-ylmethyl]-3-phenylselanyl-dihydro-furan-2-one 
• 134133-77-0 (S)-5-((2R,6S,11R)-8-Hydroxy-6,11-dimethyl-1,2,5,6-tetrahydro-4H-2,6-methano-benzo[d]azocin-3-ylmethyl)-3-phenylselanyl-dihydro-furan-2-one 
• 220106-21-8 2-(2-bromo-allyl)-4-(tert-butyl-diphenyl-silanyloxy)-1-pyrrolidin-1-yl-oct-7-en-1-one 
• 220106-42-3 2-benzyl-4-(tert-butyl-diphenyl-silanyloxy)-1-pyrrolidin-1-yl-oct-7-en-1-one 
• 220106-36-5 4-(tert-butyl-diphenyl-silanyloxy)-2-methyl-1-pyrrolidin-1-yl-oct-7-en-1-one 
• 201344-60-7 4-(tert-butyl-diphenyl-silanyloxy)-1-pyrrolidin-1-yl-oct-7-en-1-one 
• 159949-25-4 (R)-5-[3-(2,3-Dimethoxy-phenyl)-propyl]-dihydro-furan-2-one 

Relevant articles and documents

A synthetic approach to the pseudopterosins using cascade technology

A rapid synthetic entry towards the pseudopterosins, a class of diterpenes which display potent anti-inflammatory and analgesic properties, is described. The key feature of this approach is the use of a sequential intramolecular, Lewis acid mediated Friedel-Crafts alkylation - Friedel-Crafts acylation sequence, viz 14 to 15, to establish the tricyclic carbon framework.

METHOD FOR SYNTHESIZING A PRECURSOR OF A SINGLE DAIRY-LACTONE ISOMER

This disclosure provides a method for preparing a precursor of a single dairy-lactone isomer, methods of preparing a single dairy-lactone isomer, and to the organoleptic uses thereof.

ABSOLUTE CONFIGURATION OF ELDANOLIDE, THE WING GLAND PHEROMONE OF THE MALE AFRICAN CANE BORER, ELDANA SACCHARINA (WLK.) SYNTHESES OF ITS (+) AND (-) ENANTIOMERS.

Eldanolide 1, a novel terpenoid lactone pheromone, was shown to have (3S,4R) configuration by synthesis of both enantiomers and comparison of their CD with the natural pheromone.