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Ly 215840 CAS NO 137328-52-0


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CAS No.:137328-52-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Ly 215840 CAS NO 137328-52-0 is a high-purity, non-peptide small molecule compound of significant interest in advanced pharmaceutical research and development. This compound serves as a critical intermediate or active pharmaceutical ingredient (API) for investigating novel therapeutic pathways. It is primarily utilized by research institutions and pharmaceutical companies engaged in the discovery and synthesis of new drug candidates. Our supply ensures consistent quality and reliable availability to support critical R&D timelines and scale-up processes.

Application

  • Pharmaceutical Research & Development: As a key intermediate or reference standard in the synthesis of novel drug candidates.
  • Biochemical Assay Development: For use as a tool compound in high-throughput screening (HTS) and target validation studies.
  • Preclinical Studies: Sourcing material for pharmacokinetic, pharmacodynamic, and toxicology evaluations in animal models.
  • Process Chemistry & Scale-Up: Providing material for route scouting, optimization, and pilot-scale manufacturing of APIs.
  • Academic Research: Supplying universities and research institutes for fundamental studies in medicinal chemistry and pharmacology.
  • Contract Manufacturing Organizations (CMOs): Sourcing reliable raw materials for cGMP-compliant production under client-specific protocols.

Basic Information

Product Name Ly 215840
CAS No. 137328-52-0
Molecular Formula C21H23N3O4S
Molecular Weight 413.49 g/mol
Synonyms LY-215840; 1-(4-Methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-yl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide; 1H-Pyrazolo[3,4-c]pyridine-3-carboxamide, 4,5,6,7-tetrahydro-1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxo-1-piperidinyl)phenyl]-; UNII-2F8N8B8K6K; 2F8N8B8K6K; BDBM50112605; CHEMBL2103875; DTXSID701015130
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Quality Control

Every batch of Ly 215840 is manufactured and tested under strict quality management systems to ensure it meets the high standards required for pharmaceutical research. We provide comprehensive analytical data, including HPLC purity, identity confirmation (IR, NMR), and residual solvent analysis. A Certificate of Analysis (COA) is supplied with each shipment, detailing all test results against agreed specifications. Our quality systems support development under various regulatory frameworks, including cGMP for API intermediates where required.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). The product is hygroscopic (moisture-sensitive) and should be handled under anhydrous conditions to maintain stability. For long-term storage, consider storing under an inert atmosphere.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Purity (HPLC) ≥ 98.0%
Water Content (KF) ≤ 0.5%
Residual Solvents (GC) Meets ICH Q3C guidelines
Heavy Metals < 10 ppm
Assay 97.0% - 103.0% (on anhydrous basis)

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

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Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.