1-Boc-7-methylindole-3-boronic acid pinacol ester
95%
- Product Code: 39720
CAS:
1256360-03-8
| Molecular Weight: | 357.25 g./mol | Molecular Formula: | C₂₀H₂₈BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16295117 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃, dry, airtight |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester coupling partner. Its Boc-protected indole structure makes it valuable in the synthesis of complex molecules, including pharmaceuticals and biologically active compounds. The methyl group at the 7-position enhances its stability and reactivity in various transformations. It is often employed in the development of drug candidates, especially those targeting central nervous system disorders, due to the indole moiety’s prevalence in bioactive molecules. Additionally, it serves as a key intermediate in the preparation of heterocyclic compounds for material science and agrochemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $803.72 |
+
-
|
| 0.250 | 10-20 days | $1,340.73 |
+
-
|
| 1.000 | 10-20 days | $2,687.79 |
+
-
|
1-Boc-7-methylindole-3-boronic acid pinacol ester
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester coupling partner. Its Boc-protected indole structure makes it valuable in the synthesis of complex molecules, including pharmaceuticals and biologically active compounds. The methyl group at the 7-position enhances its stability and reactivity in various transformations. It is often employed in the development of drug candidates, especially those targeting central nervous system disorders, due to the indole moiety’s prevalence in bioactive molecules. Additionally, it serves as a key intermediate in the preparation of heterocyclic compounds for material science and agrochemical research.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
$0.00
$0.00
Total :