Description

6,7-Dihydrobenzo[F]Cyclopenta[A]Quinolizine-6,7,7A,8,9,10(8H)-Hexacarboxylic Acid Hexamethyl Ester is a high-purity, complex polycyclic organic compound with a multi-ester functionalized structure. This compound serves as a critical advanced intermediate in sophisticated organic synthesis, valued for its unique fused-ring system that provides a versatile scaffold for further chemical elaboration. It is primarily required by pharmaceutical R&D and specialty chemical manufacturers engaged in developing novel active ingredients and functional materials.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of complex alkaloid analogs and potential drug candidates targeting neurological and oncological pathways.
• Organic Synthesis Research: Versatile precursor for constructing polycyclic frameworks in academic and industrial research laboratories.
• Ligand and Catalyst Development: Starting material for creating novel chiral ligands or organocatalysts due to its rigid, three-dimensional structure.
• Material Science: Potential monomer or precursor for developing specialized polymers with unique thermal or optical properties.
• Fluorescent Dye & Sensor Synthesis: Intermediate in the production of advanced organic chromophores and molecular sensors.

Basic Information

Item	Detail
Product Name	6,7-Dihydrobenzo[F]Cyclopenta[A]Quinolizine-6,7,7A,8,9,10(8H)-Hexacarboxylic Acid Hexamethyl Ester
CAS No.	49616-72-0
Molecular Formula	C30H30O12
Molecular Weight	582.56 g/mol
Synonyms	Hexamethyl 6,7-dihydrobenzo[f]cyclopenta[a]quinolizine-6,7,7a,8,9,10(8H)-hexacarboxylate; Benzo[f]cyclopenta[a]quinolizine-6,7,7a,8,9,10(8H)-hexacarboxylic acid, 6,7-dihydro-, hexamethyl ester; 6,7-Dihydrobenzo[f]cyclopenta[a]quinolizine-6,7,7a,8,9,10(8H)-hexacarboxylic acid hexamethyl ester; CAS 49616-72-0
EINECS	Contact for details

Quality Control

Our production of 6,7-Dihydrobenzo[F]Cyclopenta[A]Quinolizine-6,7,7A,8,9,10(8H)-Hexacarboxylic Acid Hexamethyl Ester adheres to stringent quality protocols to ensure batch-to-batch consistency and high purity for research and development applications. Each lot is supported by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We operate under a cGMP-compliant quality management system suitable for advanced pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). The compound may be sensitive to prolonged exposure to moisture and should be handled under an inert atmosphere for long-term storage.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 97.0%
Related Substances (HPLC)	Total impurities ≤ 3.0% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%

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