(R)-3-Methylisoindolin-1-one
95%
- Product Code: 71037
CAS:
131615-22-0
| Molecular Weight: | 147.17 g./mol | Molecular Formula: | C₉H₉NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12924037 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
(R)-3-Methylisoindolin-1-one is primarily used in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its chiral structure makes it valuable in the development of enantiomerically pure drugs, particularly those targeting neurological and psychiatric disorders. It is often employed in the production of potential therapeutic agents for conditions such as depression, anxiety, and neurodegenerative diseases. Additionally, this compound is utilized in organic synthesis to create complex molecules with specific stereochemical properties, aiding in the exploration of new drug candidates and chemical entities. Its application extends to research settings, where it serves as a building block for studying structure-activity relationships in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,190.00 |
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| 0.250 | 10-20 days | ฿14,040.00 |
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| 1.000 | 10-20 days | ฿28,080.00 |
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(R)-3-Methylisoindolin-1-one
(R)-3-Methylisoindolin-1-one is primarily used in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its chiral structure makes it valuable in the development of enantiomerically pure drugs, particularly those targeting neurological and psychiatric disorders. It is often employed in the production of potential therapeutic agents for conditions such as depression, anxiety, and neurodegenerative diseases. Additionally, this compound is utilized in organic synthesis to create complex molecules with specific stereochemical properties, aiding in the exploration of new drug candidates and chemical entities. Its application extends to research settings, where it serves as a building block for studying structure-activity relationships in medicinal chemistry.
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