Description

D-Homo-17A-Oxaandrost-4-Ene-3,17-Dione Deriv. Of 2H-Phenanthro[2, 1-B] Pyran is a high-purity, complex steroid-derived compound, specifically a D-homo lactone derivative, valued for its role as a critical synthetic intermediate. This compound is essential for researchers and manufacturers developing novel pharmaceutical agents, particularly in the fields of endocrinology and oncology. It is primarily utilized by advanced pharmaceutical R&D laboratories and fine chemical synthesis facilities requiring precise molecular building blocks for complex organic synthesis.

Application

• Pharmaceutical Intermediate: A key precursor in the multi-step synthesis of novel steroid-based therapeutic agents and active pharmaceutical ingredients (APIs).
• Research & Development: Serves as a crucial building block in medicinal chemistry for the discovery and development of new drug candidates targeting hormone-related pathways.
• Fine Chemical Synthesis: Used in the production of specialized, high-value chemical entities for advanced material science and biochemical applications.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and compound identification via HPLC, GC-MS, or NMR.

Basic Information

Product Name	D-Homo-17A-Oxaandrost-4-Ene-3,17-Dione Deriv. Of 2H-Phenanthro[2, 1-B] Pyran
CAS No.	55230-47-2
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	2H-Phenanthro[2,1-b]pyran derivative of D-Homo-17a-oxaandrost-4-ene-3,17-dione; Steroid-lactone fused phenanthropyran derivative; D-Homo-17a-Oxa-4-androstene-3,17-dione Phenanthropyran Derivative; CAS 55230-47-2; [3,2-c]Pyrano[3',2':14,15]estra-4,14-diene-3,17-dione derivative (D-homo lactone); Advanced Steroid Intermediate 55230-47-2
EINECS	Contact for details

Quality Control

Our D-Homo-17A-Oxaandrost-4-Ene-3,17-Dione Deriv. Of 2H-Phenanthro[2, 1-B] Pyran is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including chromatographic purity assays and structural confirmation, to ensure it meets the high standards required for pharmaceutical research and synthesis. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with every shipment to guarantee traceability and compliance.

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 the container tightly sealed to protect from moisture and contamination.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Purity (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
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.