(R)-3,3-Dimethylbutan-2-amine hydrochloride
95%
- Product Code: 56086
CAS:
31519-54-7
| Molecular Weight: | 137.65 g./mol | Molecular Formula: | C₆H₁₆ClN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28501709 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(R)-3,3-Dimethylbutan-2-amine hydrochloride finds its primary application in the pharmaceutical industry as a chiral building block. It is used in the synthesis of various active pharmaceutical ingredients (APIs) where the specific stereochemistry is crucial for the desired biological activity. This compound is particularly valuable in the development of drugs targeting the central nervous system, where enantiomeric purity can significantly impact efficacy and safety. Additionally, it serves as an intermediate in the production of agrochemicals, contributing to the creation of more effective and selective pesticides. Its role in asymmetric synthesis also extends to academic research, where it aids in the study of chiral catalysts and enantioselective reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,341.00 |
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| 0.250 | 10-20 days | ฿3,222.00 |
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(R)-3,3-Dimethylbutan-2-amine hydrochloride
(R)-3,3-Dimethylbutan-2-amine hydrochloride finds its primary application in the pharmaceutical industry as a chiral building block. It is used in the synthesis of various active pharmaceutical ingredients (APIs) where the specific stereochemistry is crucial for the desired biological activity. This compound is particularly valuable in the development of drugs targeting the central nervous system, where enantiomeric purity can significantly impact efficacy and safety. Additionally, it serves as an intermediate in the production of agrochemicals, contributing to the creation of more effective and selective pesticides. Its role in asymmetric synthesis also extends to academic research, where it aids in the study of chiral catalysts and enantioselective reactions.
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