Description

Methyl 7-Benzyloxy-1H-Indazole-3-Carboxylate is a high-purity, advanced pharmaceutical intermediate belonging to the indazole class of heterocyclic compounds. This compound is a critical building block in the synthesis of complex active pharmaceutical ingredients (APIs), valued for its defined structure and reactivity. It is primarily utilized by research institutions and manufacturers in the pharmaceutical and biotechnology sectors for the development of new therapeutic agents.

Application

• Pharmaceutical Intermediate: A key precursor in the multi-step synthesis of novel drug candidates, particularly those targeting specific enzymatic pathways.
• API Development: Serves as a core scaffold for the research and development of new Active Pharmaceutical Ingredients with potential therapeutic applications.
• Chemical Research: Used in academic and industrial R&D laboratories for studying structure-activity relationships (SAR) and exploring new chemical entities.
• Process Chemistry: Employed in process optimization and scale-up studies for the efficient production of target molecules.
• Reference Standard: Can be supplied as a high-purity standard for analytical method development and quality control in pharmaceutical manufacturing.

Basic Information

Product Name	Methyl 7-Benzyloxy-1H-Indazole-3-Carboxylate
CAS No.	885278-65-9
Molecular Formula	C16H14N2O3
Molecular Weight	282.30 g/mol
Synonyms	Methyl 7-(benzyloxy)-1H-indazole-3-carboxylate; 7-Benzyloxy-1H-indazole-3-carboxylic acid methyl ester; 1H-Indazole-3-carboxylic acid, 7-(phenylmethoxy)-, methyl ester; Methyl 7-(phenylmethoxy)-1H-indazole-3-carboxylate; 885278-65-9; Methyl 7-O-benzyl-1H-indazole-3-carboxylate
EINECS	Contact for details

Quality Control

Our production of Methyl 7-Benzyloxy-1H-Indazole-3-Carboxylate adheres to stringent quality management protocols. Each batch is subjected to comprehensive analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide detailed Certificates of Analysis (COA) with every shipment, documenting all critical quality attributes. Our quality systems are designed to support cGMP compliance for pharmaceutical applications.

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 to prevent exposure to atmospheric moisture. Keep away from heat and incompatible materials.

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	≤ 10 ppm

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