Description

{3-[2-(Dimethylamino)Ethyl]-5-[(Pyrrolidine-1-Yl)Sulfonylmethyl]-1H-Indol-1-Yl}Methanol is a sophisticated indole-based organic compound with a complex molecular architecture designed for advanced chemical synthesis. This high-purity intermediate is critical for research and development in pharmaceutical discovery, particularly in the creation of novel therapeutic agents targeting the central nervous system. It is primarily sought by pharmaceutical R&D laboratories, biotechnology companies, and fine chemical manufacturers engaged in the synthesis of complex bioactive molecules.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates, particularly for neurological and psychiatric disorders.
• Biochemical Research: Used as a reference standard or a precursor in the study of enzyme inhibition and receptor binding assays.
• Medicinal Chemistry: Serves as a core scaffold for structure-activity relationship (SAR) studies to optimize potency and selectivity of lead compounds.
• Fine Chemical Synthesis: Employed in multi-step organic synthesis to construct complex heterocyclic systems with specific pharmacological properties.
• Contract Research & Manufacturing (CRO/CMO): Supplied to organizations specializing in custom synthesis and process development for clinical trial materials.

Basic Information

Product Name	{3-[2-(Dimethylamino)Ethyl]-5-[(Pyrrolidine-1-Yl)Sulfonylmethyl]-1H-Indol-1-Yl}Methanol
CAS No.	1018676-02-2
Molecular Formula	C19H29N3O3S
Molecular Weight	379.52 g/mol
Synonyms	1H-Indole-1-methanol, 3-[2-(dimethylamino)ethyl]-5-[(1-pyrrolidinylsulfonyl)methyl]-; 5-[(Pyrrolidine-1-sulfonyl)methyl]-3-[2-(dimethylamino)ethyl]-1H-indol-1-ylmethanol; (3-(2-(Dimethylamino)ethyl)-5-((pyrrolidin-1-ylsulfonyl)methyl)-1H-indol-1-yl)methanol; CAS 1018676-02-2; 1018676-02-2
EINECS	Contact for details

Quality Control

Our production of {3-[2-(Dimethylamino)Ethyl]-5-[(Pyrrolidine-1-Yl)Sulfonylmethyl]-1H-Indol-1-Yl}Methanol adheres to stringent quality management protocols. Each batch undergoes comprehensive analytical testing, including HPLC for purity and NMR for structural confirmation, to ensure it meets the exacting standards required for pharmaceutical research. A Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to guarantee traceability and batch-to-batch consistency.

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 (moisture-sensitive) nature, the container must be kept tightly sealed under an inert atmosphere (e.g., nitrogen or argon) after opening to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

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