Description

1-Piperidineacetamide, n-(3-Cyano-4,5,6,7-Tetrahydrobenzo[B]Thien-2-Yl)- is a high-purity, advanced pharmaceutical intermediate with a complex heterocyclic structure. This compound is valued for its role as a critical building block in the synthesis of novel active pharmaceutical ingredients (APIs), particularly those targeting central nervous system and metabolic disorders. It is primarily sought after by research institutions, custom synthesis houses, and pharmaceutical manufacturers engaged in drug discovery and process development.

Application

• Pharmaceutical Intermediate: Serves as a key precursor in the research and commercial synthesis of proprietary drug candidates.
• Drug Discovery & Development: Used in medicinal chemistry for structure-activity relationship (SAR) studies and lead optimization.
• Custom Synthesis: Employed by contract research and manufacturing organizations (CROs/CMOs) for client-specific molecule production.
• Chemical Reference Standard: Utilized as a high-purity standard for analytical method development and quality control in API manufacturing.
• Academic & Institutional Research: Applied in biochemical and pharmacological research to study new therapeutic pathways.

Basic Information

Product Name	1-Piperidineacetamide, n-(3-Cyano-4,5,6,7-Tetrahydrobenzo[B]Thien-2-Yl)-
CAS No.	58125-33-0
Molecular Formula	C16H21N3OS
Molecular Weight	303.42 g/mol
Synonyms	N-(3-Cyano-4,5,6,7-tetrahydro-1-benzothien-2-yl)-2-piperidin-1-ylacetamide; 2-Piperidin-1-yl-N-(4,5,6,7-tetrahydro-3-cyano-1-benzothiophen-2-yl)acetamide; 1-Piperidineacetamide, N-(3-cyano-4,5,6,7-tetrahydrobenzo[b]thien-2-yl)-; 58125-33-0; N-(3-Cyano-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)-2-(piperidin-1-yl)acetamide
EINECS	Contact for details

Quality Control

Our 1-Piperidineacetamide, n-(3-Cyano-4,5,6,7-Tetrahydrobenzo[B]Thien-2-Yl)- is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. A detailed Certificate of Analysis (COA) is provided with each shipment, confirming compliance with agreed specifications. We support cGMP standards for pharmaceutical intermediate production.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials. For long-term storage, consider storage under an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm

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