1-Bromo-2,5-dimethoxybenzene
97%
- Product Code: 115438
Alias:
2,5-Dimethoxybromobenzene; 1-Bromo-2,5-dimethoxybenzene
CAS:
25245-34-5
| Molecular Weight: | 217.06 g./mol | Molecular Formula: | BrC₆H₃OCH₃₂ |
|---|---|---|---|
| EC Number: | 246-756-7 | MDL Number: | MFCD00008355 |
| Melting Point: | Boiling Point: | 130-131 °C (10 mmHg) | |
| Density: | 1.44 | Storage Condition: | room temperature |
Product Description:
1-Bromo-2,5-dimethoxybenzene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biaryl compounds. Additionally, it serves as a precursor in the synthesis of dyes, pigments, and other specialty chemicals. Its methoxy groups enhance reactivity, enabling its use in various electrophilic substitution reactions. This compound is also utilized in research settings for studying reaction mechanisms and developing new synthetic methodologies.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 96.5-100 |
| Refractive Index N20/D | 1.569-1.572 |
| Specific Gravity (20/20) | 1.505-1.514 |
| Appearance | Colorless To Yellow Brown Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 2.000 | 10-20 days | ฿290.00 |
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| 10.000 | 10-20 days | ฿510.00 |
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| 50.000 | 10-20 days | ฿2,070.00 |
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| 250.000 | 10-20 days | ฿8,750.00 |
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1-Bromo-2,5-dimethoxybenzene
1-Bromo-2,5-dimethoxybenzene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biaryl compounds. Additionally, it serves as a precursor in the synthesis of dyes, pigments, and other specialty chemicals. Its methoxy groups enhance reactivity, enabling its use in various electrophilic substitution reactions. This compound is also utilized in research settings for studying reaction mechanisms and developing new synthetic methodologies.
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