Description

6-Ethyl-3-(Morpholin-4-Ylcarbonyl)-4,5,6,7-Tetrahydro-1-Benzothiophen-2-Amine (Saltdata: Free) is a high-purity, advanced pharmaceutical intermediate characterized by its complex heterocyclic structure. This compound is of significant value in modern organic synthesis, particularly for the development of novel active pharmaceutical ingredients (APIs) with targeted therapeutic effects. It is primarily sought after by research institutions and manufacturers in the pharmaceutical and biotechnology sectors for use in drug discovery and process development.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates, particularly those targeting central nervous system (CNS) disorders.
• Organic Synthesis Research: Used in academic and industrial R&D for constructing complex fused-ring systems containing thiophene and morpholine motifs.
• Preclinical Development: Serves as a critical starting material for producing compounds for pharmacological screening and toxicology studies.
• Process Chemistry: Employed in route scouting and optimization for the scalable production of potential active pharmaceutical ingredients (APIs).
• Chemical Reference Standard: Supplied as a high-purity standard for analytical method development and quality control in pharmaceutical manufacturing.

Basic Information

Product Name	6-Ethyl-3-(Morpholin-4-Ylcarbonyl)-4,5,6,7-Tetrahydro-1-Benzothiophen-2-Amine (Saltdata: Free)
CAS No.	590351-57-8
Molecular Formula	C15H22N2O2S
Molecular Weight	294.41 g/mol
Synonyms	6-Ethyl-3-(morpholine-4-carbonyl)-4,5,6,7-tetrahydro-1-benzothiophen-2-amine; 2-Amino-6-ethyl-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid morpholide; 590351-57-8; 6-Ethyl-3-(morpholin-4-ylcarbonyl)-4,5,6,7-tetrahydro-1-benzothiophen-2-amine; 4,5,6,7-Tetrahydro-6-ethyl-3-(4-morpholinylcarbonyl)-1-benzothiophen-2-amine
EINECS	Contact for details

Quality Control

Our production of 6-Ethyl-3-(Morpholin-4-Ylcarbonyl)-4,5,6,7-Tetrahydro-1-Benzothiophen-2-Amine adheres to stringent quality management protocols. Every batch undergoes comprehensive analytical testing, including HPLC for purity, NMR and IR for structural confirmation, and residual solvent analysis. We provide a detailed Certificate of Analysis (COA) with each shipment, ensuring full traceability and compliance with cGMP guidelines where applicable for pharmaceutical intermediate use.

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 nature, the container must be kept tightly sealed after opening to prevent moisture absorption, which may affect stability and handling properties. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residual Solvents (GC)	Meets ICH guidelines
Heavy Metals	≤ 20 ppm

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