(R)-2-((4-Nitrophenethyl)amino)-1-phenylethanol hydrochloride CAS: 521284-21-9
| Product Parameters | |
|---|---|
| Catalog No. | BK0U57 |
| CAS.RN | 521284-21-9 |
| Molecular Formula | C16H19ClN2O3 |
| Molecular Weight | 322.79 g/mol |
| Purity | NLT 98% |
| Synonyms |
Product Overview
(R)-2-((4-nitrophenylethyl)amino)-1-phenylethanol hydrochloride is a high-optical-purity pharmaceutical intermediate widely used in the construction and synthesis of chiral drug molecules. This product possesses a well-defined stereochemical structure and stable functional group properties, making it suitable for drug development, process development, and pilot-scale amplification stages. It can meet diverse customer needs in small-scale research, process optimization, and large-scale production, and is an important precursor compound for the synthesis of nitrogen-containing heterocyclic drugs.
Applications
- Drug molecule structure construction
- Key intermediates in chiral synthesis
- Process route development and optimization
- Pilot-scale production and commercialization
- Customized synthesis and impurity control
Quality & Supply Capability
English Name: (R)-2-((4-Nitrophenethyl)amino)-1-phenylethanol hydrochloride Properties: This product is a white to off-white crystalline powder containing aminomethyl and nitrophenyl structures. It exhibits good chemical stability and optical activity, making it suitable for various organic synthesis reactions. Storage Recommendations: Store in a sealed, light-protected, and dry place, subject to the specific COA/MSDS. Supply Capabilities: Samples, gram-level, kilogram-level, commercial batches Packaging Specifications: Aluminum foil bags, fluorinated bottles, cardboard drums, customized packaging Documentation Support: COA, MSDS, HPLC, NMR, etc. We provide a full-process service from laboratory sample supply to small-scale preparation, pilot-scale amplification, and customized batch production. We can flexibly adjust purity standards, impurity control requirements, packaging specifications, and delivery cycles according to customer needs, while providing a complete quality documentation system to ensure that products meet GMP and R&D compliance requirements. Our technical team can assist customers throughout the process development, route optimization, and project transformation, helping them efficiently advance the new drug development process.
Why Choose Bioncan
Focused on pharmaceutical intermediates, possessing a rich product line and professional experience. Full-scale supply capabilities, covering needs from laboratory to commercial production. Provides complete quality control documentation to ensure product quality and compliance. Supports customized needs, meeting the specific specifications and technical requirements of different customers. Provides supporting process optimization technology to help customers achieve efficient and economical process development.
Customers are responsible for ensuring compliance with applicable patent, regulatory, and import/export requirements in their respective jurisdictions.
Online Consulting
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