(3-BroMo-4-Methylphenyl)Methanol
98%
- Product Code: 36645
CAS:
68120-35-4
| Molecular Weight: | 201.06046 g./mol | Molecular Formula: | C₈H₉BrO |
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| EC Number: | MDL Number: | ||
| Melting Point: | 38-42℃ | Boiling Point: | 283.4±25.0 ℃ at 760 mmHg |
| Density: | 1.481±0.06 g/cm3 | Storage Condition: | room temperature |
Product Description:
The primary application of (3-Bromo-4-Methylphenyl)Methanol is in the field of organic synthesis, where it serves as a versatile intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its structure, featuring both a bromine atom and a hydroxyl group, makes it a valuable building block for constructing complex molecules. In pharmaceutical research, it is often utilized in the development of active pharmaceutical ingredients (APIs) due to its ability to undergo further functionalization. Additionally, it finds use in the synthesis of fine chemicals and dyes, where its aromatic and reactive properties are leveraged to create specific molecular architectures. Its role in cross-coupling reactions is also notable, as it can participate in processes like Suzuki or Sonogashira couplings to form carbon-carbon bonds, which are essential in many synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,872.00 |
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| 5.000 | 10-20 days | ฿6,057.00 |
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(3-BroMo-4-Methylphenyl)Methanol
The primary application of (3-Bromo-4-Methylphenyl)Methanol is in the field of organic synthesis, where it serves as a versatile intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its structure, featuring both a bromine atom and a hydroxyl group, makes it a valuable building block for constructing complex molecules. In pharmaceutical research, it is often utilized in the development of active pharmaceutical ingredients (APIs) due to its ability to undergo further functionalization. Additionally, it finds use in the synthesis of fine chemicals and dyes, where its aromatic and reactive properties are leveraged to create specific molecular architectures. Its role in cross-coupling reactions is also notable, as it can participate in processes like Suzuki or Sonogashira couplings to form carbon-carbon bonds, which are essential in many synthetic pathways.
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