(R)-tert-Butyl (4-cyano-2,3-dihydro-1H-inden-1-yl)carbamate
97%
- Product Code: 37288
CAS:
1306763-30-3
| Molecular Weight: | 258.32 g./mol | Molecular Formula: | C₁₅H₁₈N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28502614 | |
| Melting Point: | Boiling Point: | 357.7±37.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of chiral molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a cyano group and a carbamate moiety, makes it valuable for constructing complex organic frameworks with high stereochemical control. It is often employed in the preparation of enantiomerically pure compounds, which are crucial in the production of drugs targeting specific biological pathways, such as enzyme inhibitors or receptor modulators. Additionally, its stability and reactivity under various conditions make it suitable for use in multi-step synthetic processes, contributing to the efficient and scalable production of therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $68.32 |
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| 0.250 | 10-20 days | $136.90 |
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(R)-tert-Butyl (4-cyano-2,3-dihydro-1H-inden-1-yl)carbamate
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of chiral molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a cyano group and a carbamate moiety, makes it valuable for constructing complex organic frameworks with high stereochemical control. It is often employed in the preparation of enantiomerically pure compounds, which are crucial in the production of drugs targeting specific biological pathways, such as enzyme inhibitors or receptor modulators. Additionally, its stability and reactivity under various conditions make it suitable for use in multi-step synthetic processes, contributing to the efficient and scalable production of therapeutic agents.
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