Description

Spiro[Benzofuran-2(3H),4'-Piperidine], 1'-(Phenylmethyl)- is a high-value, complex spirocyclic organic compound featuring a benzofuran moiety fused to a piperidine ring system. This unique molecular architecture makes it a critical advanced pharmaceutical intermediate for the research and development of novel therapeutic agents. It is primarily sought after by pharmaceutical R&D laboratories and fine chemical manufacturers engaged in the synthesis of complex bioactive molecules.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of potential drug candidates, particularly in central nervous system (CNS) and other therapeutic areas.
• Medicinal Chemistry Research: Used as a core scaffold for structure-activity relationship (SAR) studies and the discovery of new chemical entities.
• Organic Synthesis Reference Standard: Employed as a pure standard for analytical method development and validation in QC laboratories.
• Process Chemistry Development: Utilized in scaling up synthetic routes for pilot and commercial-scale production of target molecules.
• Academic & Institutional Research: A valuable compound for research in synthetic organic chemistry and heterocyclic compound studies.

Basic Information

Product Name	Spiro[Benzofuran-2(3H),4'-Piperidine], 1'-(Phenylmethyl)-
CAS No.	71916-71-7
Molecular Formula	C19H19NO
Molecular Weight	277.36 g/mol
Synonyms	1'-Benzylspiro[benzofuran-2(3H),4'-piperidine]; 1'-(Phenylmethyl)spiro[benzofuran-2(3H),4'-piperidine]; 1'-Benzyl-1,3-dihydrospiro[benzofuran-2,4'-piperidine]; Spiro[1,3-dihydro-2-benzofuran-2,4'-piperidine], 1'-benzyl-; 1'-Benzylspiro[1,3-dihydro-2-benzofuran-2,4'-piperidine]; 71916-71-7; 1'-(Phenylmethyl)spiro[benzofuran-2(3H),4'-piperidine]
EINECS	Contact for details

Quality Control

Our production of Spiro[Benzofuran-2(3H),4'-Piperidine], 1'-(Phenylmethyl)- adheres to stringent quality management protocols. Every batch undergoes comprehensive analytical testing, including HPLC, GC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide a detailed Certificate of Analysis (COA) with each shipment, confirming compliance with agreed specifications. Our quality system is designed to support cGMP requirements for advanced pharmaceutical intermediates.

Storage

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

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Single Unknown Impurity (HPLC)	≤ 0.5%

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