p-Tolylmagnesium bromide
1.0 M solution in THF, MkSeal
- Product Code: 88905
Alias:
4-Methylphenylmagnesium bromide
CAS:
4294-57-9
| Molecular Weight: | 195.34 g./mol | Molecular Formula: | C₇H₇BrMg |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00000040 | |
| Melting Point: | Boiling Point: | 65-67 °C | |
| Density: | 1.002 g/mL at 25 °C | Storage Condition: | 2~8 ℃ |
Product Description:
p-Tolylmagnesium bromide is widely used in organic synthesis as a Grignard reagent. It is particularly valuable for forming carbon-carbon bonds, making it essential in the production of complex organic molecules. This reagent is commonly employed in the synthesis of pharmaceuticals, where it introduces the p-tolyl group into target compounds, enhancing their structural diversity and biological activity. Additionally, it is used in the preparation of fine chemicals and intermediates for agrochemicals. Its reactivity with various electrophiles, such as carbonyl compounds, enables the creation of alcohols, ketones, and other functionalized derivatives. This makes it a versatile tool in research and industrial chemistry for constructing tailored organic structures.
Product Specification:
| Test | Specification |
|---|---|
| CONCENTRATIONTITRATION SEC-BUTANOL | 0.95-1.1 |
| APPEARANCE | BLACK LIQUID |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 100.000 | 10-20 days | ฿2,640.00 |
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| 500.000 | 10-20 days | ฿6,860.00 |
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| 1000.000 | 10-20 days | ฿13,050.00 |
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p-Tolylmagnesium bromide
p-Tolylmagnesium bromide is widely used in organic synthesis as a Grignard reagent. It is particularly valuable for forming carbon-carbon bonds, making it essential in the production of complex organic molecules. This reagent is commonly employed in the synthesis of pharmaceuticals, where it introduces the p-tolyl group into target compounds, enhancing their structural diversity and biological activity. Additionally, it is used in the preparation of fine chemicals and intermediates for agrochemicals. Its reactivity with various electrophiles, such as carbonyl compounds, enables the creation of alcohols, ketones, and other functionalized derivatives. This makes it a versatile tool in research and industrial chemistry for constructing tailored organic structures.
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