Description

1(3Ah)-Pentalenone, 3-Amino-4,5,6,6A-Tetrahydro-3A-Hydroxy-, (3Ar,6Ar)-Rel- (9Ci) is a complex, stereochemically defined bicyclic compound featuring both amino and hydroxyl functional groups, making it a valuable chiral building block for advanced organic synthesis. Its unique fused-ring structure and functional group array are critical for constructing complex molecular architectures with high stereochemical fidelity. This intermediate is primarily sought by research and development teams in the pharmaceutical and agrochemical sectors for the synthesis of novel active ingredients and fine chemicals.

Application

• Pharmaceutical Intermediate: Serves as a key chiral synthon in the research and development of new drug candidates, particularly for complex natural product analogs and bioactive molecules.
• Agrochemical Synthesis: Used in the development of advanced pesticides and herbicides where its specific stereochemistry can influence biological activity.
• Organic Synthesis Research: Acts as a versatile building block in academic and industrial laboratories for methodological studies in stereoselective synthesis and ring system construction.
• Fine Chemical Production: Employed in the multi-step synthesis of specialty chemicals, flavors, and fragrances requiring precise molecular frameworks.
• Material Science Precursor: Potential use in the synthesis of specialized polymers or ligands for catalytic systems due to its functional handles.

Basic Information

Product Name	1(3Ah)-Pentalenone, 3-Amino-4,5,6,6A-Tetrahydro-3A-Hydroxy-, (3Ar,6Ar)-Rel- (9Ci)
CAS No.	455893-06-8
Molecular Formula	C8H13NO2
Molecular Weight	155.19 g/mol
Synonyms	rel-(3aR,6aR)-3-Amino-3a-hydroxy-1,2,3,3a,4,5,6,6a-octahydropentalen-1-one; 3-Amino-3a-hydroxy-1,2,3,3a,4,5,6,6a-octahydropentalen-1-one (rel-(3aR,6aR)-); 455893-06-8; 1(3aH)-Pentalenone, 3-amino-4,5,6,6a-tetrahydro-3a-hydroxy-, (3aR,6aR)-rel-; Amino-hydroxy-octahydropentalenone
EINECS	Contact for details

Quality Control

Our 1(3Ah)-Pentalenone derivative is produced under strict quality management protocols to ensure batch-to-batch consistency and high purity, essential for sensitive synthetic applications. Each lot is characterized using advanced analytical techniques including HPLC, GC, NMR, and mass spectrometry. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to support your quality assurance and regulatory documentation needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric moisture. For long-term storage, consider using desiccants or an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Specific Rotation	Contact for details

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