Product Overview

3-O-9-azabicyclic [3.3.1]nonane-7-carboxylic acid ethyl ester is an important pharmaceutical intermediate widely used in the synthesis of innovative drugs such as antiviral and antitumor drugs, exhibiting high structural specificity and reactivity. This compound is suitable for the early stages of drug development, including molecular construction, small-scale preparation, pilot-scale amplification, and commercial production. It is a key starting material for synthesizing complex nitrogen-containing heterocyclic compounds, providing customers with a stable and efficient raw material supply.

Applications

• Antiviral drug synthesis
• Development of antitumor drug intermediates
• Key starting materials for organic synthesis
• Customized synthesis of pharmaceutical intermediates
• Optimization of drug process routes

Quality & Supply Capability

English Name: Ethyl 3-oxo-9-azabicyclo[3.3.1]nonane-7-carboxylate Properties: This product is a white to off-white crystalline powder with a stable nitrogen heterocyclic structure and good chemical stability. It contains ketone and ester functional groups and is suitable for various organic synthesis reactions. Storage Recommendations: Store in a sealed, light-protected, and dry place, subject to the COA/MSDS. Supply Capabilities: Samples, gram-level, kilogram-level, commercial batches Packaging Specifications: Aluminum foil bags, fluorinated bottles, cardboard drums, customized packaging Document Support: COA, MSDS, HPLC, NMR, etc. We provide a full-process service from laboratory sample supply to small-scale preparation, pilot-scale amplification, and customized batch production. We can flexibly formulate supply solutions according to customers' requirements for purity, impurity control, packaging specifications, delivery cycle, and quality documents. At the same time, we have a professional technical support team to assist customers in process development, route optimization, and project transformation, ensuring stable supply and efficient application of products at different stages.

Why Choose Bioncan

Focused on pharmaceutical intermediates, possessing extensive synthesis experience and technological expertise. Full-scale supply capability, covering needs from laboratory to commercial production. Provides complete quality control documentation to meet GMP and regulatory requirements. Supports customized needs, adjusting purity, impurity control, and packaging specifications according to customer requirements. Provides supporting process optimization and scale-up technologies to help customers achieve efficient commercialization.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 115956-05-3, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.