(R)-1-(4-Nitrophenyl)ethanamine hydrochloride
97%
- Product Code: 71641
CAS:
57233-86-0
| Molecular Weight: | 202.64 g./mol | Molecular Formula: | C₈H₁₁ClN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 248-250°C | Boiling Point: | 321.3°C |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
(R)-1-(4-Nitrophenyl)ethanamine hydrochloride is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block in the development of enantiomerically pure compounds, which are crucial for creating drugs with specific therapeutic effects. This compound is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the stereochemistry plays a significant role in the drug's efficacy and safety. Additionally, it is utilized in asymmetric synthesis processes to produce intermediates for various biologically active molecules. Its application extends to research focused on understanding the pharmacological properties of chiral amines and their derivatives.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,750.00 |
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| 1.000 | 10-20 days | ฿4,150.00 |
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(R)-1-(4-Nitrophenyl)ethanamine hydrochloride
(R)-1-(4-Nitrophenyl)ethanamine hydrochloride is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block in the development of enantiomerically pure compounds, which are crucial for creating drugs with specific therapeutic effects. This compound is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the stereochemistry plays a significant role in the drug's efficacy and safety. Additionally, it is utilized in asymmetric synthesis processes to produce intermediates for various biologically active molecules. Its application extends to research focused on understanding the pharmacological properties of chiral amines and their derivatives.
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