![Tert-Butyl 3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate CAS 478837-18-2](/uploads/202340914/tert-butyl-3-hydroxy-8-azabicyclo-3-2-1433520c3-b1f8-4f40-acc8-bb7cfa2e415e.jpg)
Tert-Butyl 3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate CAS 478837-18-2
Molecular Formula: C12H21NO3
Molecular Weight: 227.304
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We can provide you with a certificate of analysis (COA), method of analysis (MOA), route of synthesis (ROS), and material safety data sheet (MSDS) for tert-Butyl 3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate CAS 478837-18-2
Chemical Properties:
Boiling point: 327.9±35.0 °C at 760 mmHg
Density: 1.1±0.1 g/cm3
Synonyms: 2-Methyl-2-propanyl3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate;N-Boc-3-hydroxy-8-azabicyclo[3.2.1]octane;8-Azabicyclo[3.2.1]octane-8-carboxyliChemicalbookcacid,3-hydroxy-,1,1-dimethylethylester;3-hydroxy-8-aza-bicyclo[3.2.1]octane-8-carboxylicacid,tert-butylester;1-(METHYLSULFONYL)PIPERIDIN-4-AMINEHYDR
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Purity and quality control are achieved through the use of intermediates in the development and optimization of synthetic pathways for APIs. This process comprises purifying stages to eliminate contaminants, ensuring that the finished medicine product fulfills the quality and safety criteria imposed by regulatory authorities such as the FDA.
Chiral Resolution: Pharmaceutical intermediates are frequently employed to create enantiomerically pure drugs. Because distinct enantiomers of the same chemical can have dramatically different biological activities and effects, chirality is critical in medicine development. Intermediates are altered to generate the desired enantiomer, lowering the possibility of undesirable side effects.
Intermediates play an important role in the creation of scalable and cost-effective manufacturing processes. Chemists and engineers create and optimize synthetic methods that are efficient, environmentally friendly, and economically feasible for large-scale production using intermediates.
Intermediates play a significant role in the creation of generic copies of branded medications. When patents expire, generic producers must frequently reverse-engineer the synthesis of APIs and intermediates in order to develop lower-cost copies of pharmaceuticals.Conclusion - It is critical to have access to reliable sources.
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