Description

n-Acryloyl-(2S)-Bornane-10,2-Sultam is a high-value, chiral auxiliary and building block derived from camphorsultam. This compound matters for its ability to impart exceptional stereoselectivity in a wide range of asymmetric synthesis reactions, enabling the production of enantiomerically pure intermediates. It is critically needed by R&D chemists and process development scientists in the pharmaceutical, agrochemical, and advanced materials sectors for creating novel active ingredients and functional molecules with precise chiral configurations.

Application

• Asymmetric Synthesis: Employed as a versatile chiral auxiliary in Michael additions, alkylations, and Diels-Alder reactions to control stereochemistry.
• Pharmaceutical Intermediates: Key building block for the synthesis of enantiomerically pure active pharmaceutical ingredients (APIs) and complex natural product analogs.
• Agrochemical Development: Used in the research and production of chiral pesticides and herbicides where specific stereoisomers exhibit enhanced activity.
• Material Science: Serves as a precursor for chiral monomers in the development of specialty polymers with advanced optical or mechanical properties.
• Catalyst Ligand Synthesis: A starting material for constructing sophisticated chiral ligands used in homogeneous catalysis.
• Academic & Industrial R&D: A fundamental tool in research laboratories for methodological development in organic and medicinal chemistry.

Basic Information

Product Name	n-Acryloyl-(2S)-Bornane-10,2-Sultam
CAS No.	119944-89-7
Molecular Formula	C₁₃H₁₉NO₃S
Molecular Weight	269.36 g/mol
Synonyms	(2S)-3-Acryloyl-1,7,7-trimethylbicyclo[2.2.1]heptane-2-sulfonamide; (2S)-Bornane-10,2-sultam acrylamide; (2S)-3-Acryloyl-2-bornanesulfonamide; (2S)-N-Acryloylbornane-10,2-sultam; (2S)-N-Acryloyl-10,2-camphorsultam; Acryloyl-(2S)-camphorsultam; (S)-N-Acryloylcamphorsultam; (S)-N-Acryloyl-10,2-bornanesultam
EINECS	Contact for details

Quality Control

Our n-Acryloyl-(2S)-Bornane-10,2-Sultam is produced under strict quality management systems. Each batch undergoes rigorous analytical testing, including chiral purity assessment by HPLC, to ensure it meets the high standards required for sensitive asymmetric synthesis. Certificates of Analysis (COA) detailing identity, purity, and enantiomeric excess are provided and available upon request to support your quality assurance and regulatory documentation.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at room temperature (15-25°C). This material is light-sensitive and should be handled and stored away from direct light exposure to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Enantiomeric Excess (Chiral HPLC)	≥ 99.0%
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.