Description

(2R,3S) 5-Hexene-2-Sulfonamide, 3-Methyl is a high-purity, chiral sulfonamide derivative characterized by its specific stereochemistry and functionalized alkene chain. This compound matters as a sophisticated building block in modern organic synthesis, enabling the creation of complex molecules with precise three-dimensional structures. It is primarily needed by research chemists and process development scientists in the pharmaceutical and agrochemical industries for applications in asymmetric synthesis, medicinal chemistry, and the development of novel active ingredients.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the research and development of new active pharmaceutical ingredients (APIs), particularly in oncology and central nervous system (CNS) drug discovery.
• Asymmetric Catalyst Ligand Precursor: Used in the synthesis of novel chiral ligands for transition metal catalysis, enabling enantioselective transformations.
• Agrochemical Research: Serves as a building block for developing new chiral herbicides, fungicides, and plant growth regulators with improved efficacy and environmental profiles.
• Material Science: Potential monomer or cross-linking agent in the development of specialty polymers with unique optical or mechanical properties.
• Chemical Biology Probe Development: Utilized in the synthesis of molecular probes to study enzyme mechanisms and protein-ligand interactions due to its sulfonamide moiety.

Basic Information

Product Name	(2R,3S) 5-Hexene-2-Sulfonamide, 3-Methyl
CAS No.	1638587-36-6
Molecular Formula	C7H13NO2S
Molecular Weight	175.25 g/mol
Synonyms	(2R,3S)-3-Methyl-5-hexene-2-sulfonamide; 3-Methyl-5-hexene-2-sulfonamide, (2R,3S)-; 5-Hexene-2-sulfonamide, 3-methyl-, (2R,3S)-; (2R,3S)-3-Methylhex-5-ene-2-sulfonamide; (2R,3S)-3-Methyl-5-hexenesulfonamide; (2R,3S)-3-Methylpent-4-ene-1-sulfonamide (alternative numbering); Chiral 3-Methyl-5-hexenesulfonamide
EINECS	Contact for details

Quality Control

Our (2R,3S) 5-Hexene-2-Sulfonamide, 3-Methyl is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including chiral purity verification by HPLC, to ensure compliance with exacting research and development standards. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and enantiomeric excess is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to prevent moisture absorption. Store away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Chiral Purity (Enantiomeric Excess)	≥ 99.0% ee
Melting Point	Contact for details
Loss on Drying	≤ 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.