Description

(S)-(-)-2-((1-Hydroxy-3,3-Dimethylbutan-2-Ylimino)Methyl)-4,6-Diiodophenol, 97% is a high-purity chiral organic compound featuring a phenol core functionalized with iodine atoms and a complex imino-alcohol side chain. This specific enantiomer is valued for its role as a sophisticated ligand precursor or synthetic intermediate in advanced chemical synthesis. It is primarily utilized by research institutions and pharmaceutical development companies engaged in asymmetric catalysis, medicinal chemistry, and materials science.

Application

• Asymmetric Catalyst Ligand Synthesis: Serves as a key chiral building block for constructing novel ligands used in enantioselective metal-catalyzed reactions.
• Pharmaceutical Intermediate: Employed in the research and development of active pharmaceutical ingredients (APIs) requiring specific stereochemistry.
• Organic Electronic Materials Research: Investigated as a potential component in the synthesis of organic semiconductors or photoactive materials due to its halogenated aromatic structure.
• Chemical Biology Probes: Used to develop molecular probes for studying enzyme activity or biological pathways, leveraging its unique structural motifs.
• Academic & Industrial R&D: A critical reagent for methodological development in synthetic organic chemistry laboratories worldwide.

Basic Information

Product Name	(S)-(-)-2-((1-Hydroxy-3,3-Dimethylbutan-2-Ylimino)Methyl)-4,6-Diiodophenol, 97%
CAS No.	477339-39-2
Molecular Formula	C13H17I2NO2
Molecular Weight	473.09 g/mol
Synonyms	(S)-2-[(1-Hydroxy-3,3-dimethylbutan-2-ylidene)amino]methyl]-4,6-diiodophenol; (S)-(-)-2-((1-Hydroxy-3,3-dimethyl-2-butylimino)methyl)-4,6-diiodophenol; 4,6-Diiodo-2-[[(2S)-1-hydroxy-3,3-dimethyl-2-butylidene]amino]methyl]phenol; (S)-enantiomer of a diiodophenol Schiff base; Chiral diiodophenol derivative; Contact for details on other aliases.
EINECS	Contact for details

Quality Control

Our 97% grade of this chiral compound is produced under strict quality protocols to ensure batch-to-batch consistency and enantiomeric purity. All materials are characterized by advanced analytical techniques including HPLC, chiral analysis, NMR, and mass spectrometry. A comprehensive Certificate of Analysis (COA) detailing purity, chiral excess, and impurity profiles is provided with each shipment to support your critical R&D and scale-up activities.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This compound is light-sensitive and easily oxidized; for long-term storage, consider keeping the container under an inert atmosphere such as argon or nitrogen to maintain optimal purity and stability.

Specification

Item	Specification
Appearance	Off-white to light yellow powder or crystalline solid
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Chiral Purity (Chiral HPLC)	≥ 99.0% e.e.
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.