6,7-Dichloro-2,3-dihydro-1H-inden-1-one
95%
- Product Code: 57050
CAS:
68755-30-6
| Molecular Weight: | 201.05 g./mol | Molecular Formula: | C₉H₆Cl₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16249552 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
6,7-Dichloro-2,3-dihydro-1H-inden-1-one is primarily utilized in the field of organic synthesis as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure makes it a valuable building block for the development of compounds with potential biological activity. In pharmaceutical research, it is often employed in the synthesis of molecules that target specific enzymes or receptors, contributing to the discovery of new drugs. Additionally, it finds application in the creation of herbicides and pesticides, where its derivatives can exhibit potent activity against weeds or pests. The compound’s versatility in chemical reactions, such as cyclization and functional group transformations, further enhances its utility in industrial and academic research settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $370.21 |
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| 0.250 | 10-20 days | $555.32 |
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| 1.000 | 10-20 days | $1,111.00 |
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6,7-Dichloro-2,3-dihydro-1H-inden-1-one
6,7-Dichloro-2,3-dihydro-1H-inden-1-one is primarily utilized in the field of organic synthesis as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure makes it a valuable building block for the development of compounds with potential biological activity. In pharmaceutical research, it is often employed in the synthesis of molecules that target specific enzymes or receptors, contributing to the discovery of new drugs. Additionally, it finds application in the creation of herbicides and pesticides, where its derivatives can exhibit potent activity against weeds or pests. The compound’s versatility in chemical reactions, such as cyclization and functional group transformations, further enhances its utility in industrial and academic research settings.
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