For professionals in the chemical and pharmaceutical industries, a thorough understanding of product specifications is fundamental to ensuring successful research, development, and manufacturing outcomes. This article focuses on the key specifications of (2E)-2-(1,2,6,7-tetrahydrocyclopenta[e][1]benzofuran-8-ylidene)acetonitrile (CAS: 196597-79-2), a crucial intermediate widely used in the synthesis of Ramelteon and other pharmaceutical compounds.
The primary specification for any chemical intermediate is its purity, often denoted by an assay percentage. For (2E)-2-(1,2,6,7-tetrahydrocyclopenta[e][1]benzofuran-8-ylidene)acetonitrile, a common and desirable purity level is ≥98.0%. This high assay indicates a product that is largely free from impurities, which is critical for downstream reactions in API synthesis to avoid unwanted side reactions, reduce purification challenges, and ensure the final API meets regulatory standards.
Appearance is another important physical characteristic. This intermediate is typically described as a white to yellow powder. Consistency in appearance from batch to batch is a good indicator of reliable manufacturing processes and quality control by the supplier. Any significant deviation from this expected appearance could signal an issue with the product.
Other physical and chemical properties, while sometimes less critical for initial procurement, provide valuable insights for handling, storage, and reaction optimization. These include:
Packaging is also a key specification, typically offered in drums (e.g., 25 kg/drum) and customizable according to customer requirements. Proper storage, often in a cool, ventilated place, is recommended to maintain product integrity.
For professionals looking to purchase (2E)-2-(1,2,6,7-tetrahydrocyclopenta[e][1]benzofuran-8-ylidene)acetonitrile, understanding these specifications is vital. It enables informed decision-making, facilitates effective communication with manufacturers and suppliers, and ultimately contributes to the successful execution of pharmaceutical projects. Always ensure that the product you procure aligns with these critical specifications for optimal results.
Manufacturing Facilities






Professional Export Experience
to Global Customers
1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;
2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;
3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).
A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.
A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.
A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.