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11-(3-Methylamino-1-Azetidinyl)Dibenz[B,E]Oxepin CAS NO 73927-73-8


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CAS No.:73927-73-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

11-(3-Methylamino-1-Azetidinyl)Dibenz[B,E]Oxepin is a high-purity, advanced pharmaceutical intermediate with a complex heterocyclic structure. This compound is critical for research and development in medicinal chemistry, particularly for synthesizing novel active pharmaceutical ingredients (APIs). It is primarily utilized by pharmaceutical R&D laboratories, contract research organizations (CROs), and fine chemical manufacturers targeting the development of new therapeutic agents.

Application

  • Pharmaceutical Intermediate: Key building block in the synthesis of novel drug candidates, particularly those targeting central nervous system (CNS) disorders.
  • Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and lead optimization processes for new chemical entities.
  • API Development: Serves as a precursor in the multi-step synthesis of complex active pharmaceutical ingredients.
  • Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.
  • Academic Research: Utilized in university and institutional labs for pharmacological and synthetic organic chemistry studies.
  • Pre-clinical Development: Employed in the production of compounds for pharmacological profiling and toxicology studies.

Basic Information

Product Name 11-(3-Methylamino-1-Azetidinyl)Dibenz[B,E]Oxepin
CAS No. 73927-73-8
Molecular Formula C21H24N2O
Molecular Weight 320.43 g/mol
Synonyms 11-(3-Methylaminoazetidin-1-yl)dibenz[b,e]oxepin; Dibenz[b,e]oxepin, 11-(3-(methylamino)-1-azetidinyl)-; 11-(3-Methylamino-1-azetidinyl)dibenzoxepin; 73927-73-8; UNII-9K5N5V3A3F; 9K5N5V3A3F; SCHEMBL218062; BDBM50389359; AKOS025147269
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Quality Control

Our 11-(3-Methylamino-1-Azetidinyl)Dibenz[B,E]Oxepin is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and NMR/IR for structural confirmation, to ensure it meets the high standards required for pharmaceutical R&D. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting identity, purity, and impurity profiles.

Storage

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

Specification

Item Specification
Appearance White to off-white solid
Identification (IR) Conforms to structure
Identification (HPLC) Retention time matches reference
Purity (HPLC) ≥ 98.0%
Related Substances (HPLC) Any individual impurity ≤ 0.5%
Total Impurities ≤ 2.0%
Residual Solvents (GC) Meets ICH Q3C guidelines
Water Content (KF) ≤ 0.5%

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

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