Description

Benzyl 5-Fluoropiperidin-3-Ylcarbamate Hydrochloride (Wx601161) is a high-purity, advanced pharmaceutical intermediate with the CAS number 1356342-49-8. This compound is a critical building block in modern medicinal chemistry, valued for its role in the synthesis of novel active pharmaceutical ingredients (APIs). It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of new therapeutic agents, particularly within central nervous system (CNS) and oncology research pipelines.

Application

• Pharmaceutical Intermediate: A key synthetic precursor in the research and development of new drug candidates.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and lead optimization for novel therapeutics.
• API Synthesis: Serves as a crucial building block in the multi-step synthesis of complex active pharmaceutical ingredients.
• Preclinical & Clinical Development: Supplied for the production of compounds used in pharmacological testing and early-stage clinical trials.
• Contract Manufacturing (CMO/CDMO): Sourced by contract research and manufacturing organizations for client-specific synthesis projects.
• Chemical Reference Standard: Can be supplied as a high-purity standard for analytical method development and quality control.

Basic Information

Product Name	Benzyl 5-Fluoropiperidin-3-Ylcarbamate Hydrochloride (Wx601161)
CAS No.	1356342-49-8
Molecular Formula	C14H20ClFN2O2
Molecular Weight	302.77 g/mol
Synonyms	Benzyl N-(5-Fluoropiperidin-3-yl)carbamate hydrochloride; 3-[[(Benzyloxy)carbonyl]amino]-5-fluoropiperidine hydrochloride; 5-Fluoro-3-piperidinamine, N-[(phenylmethoxy)carbonyl]-, hydrochloride (1:1); Carbamic acid, N-(5-fluoro-3-piperidinyl)-, phenylmethyl ester, hydrochloride
EINECS	Contact for details

Quality Control

Our Benzyl 5-Fluoropiperidin-3-Ylcarbamate Hydrochloride is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity, NMR and IR for structural confirmation, and tests for residual solvents and heavy metals to ensure it meets the stringent requirements for pharmaceutical R&D. A comprehensive Certificate of Analysis (COA) is provided with every shipment, detailing all specifications and test results.

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). This product is hygroscopic (moisture-sensitive) and must be kept under an inert atmosphere (e.g., nitrogen or argon) after opening to prevent degradation. Keep away from heat and incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residual Solvents (GC)	Meets ICH Q3C guidelines
Heavy Metals	< 20 ppm
Single Unknown Impurity (HPLC)	≤ 0.5%
Total Impurities (HPLC)	≤ 2.0%

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