Allylmagnesium chloride
2.0 M solution in THF ,MkSeal
- Product Code: 88895
Alias:
Allyl Magnesium Chloride; Allyl Magnesium Chloride
CAS:
2622-05-1
| Molecular Weight: | 100.83 g./mol | Molecular Formula: | C₃H₅ClMg |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00000473 | |
| Melting Point: | -21°C | Boiling Point: | 66°C |
| Density: | 0.995 g/mL at 25 °C | Storage Condition: | 2~8 ℃ |
Product Description:
Allylmagnesium chloride is widely used in organic synthesis as a Grignard reagent, which is essential for forming carbon-carbon bonds. It is particularly valuable in the production of allylic compounds, which are important intermediates in the manufacture of pharmaceuticals, agrochemicals, and fine chemicals. The reagent is also employed in the synthesis of complex organic molecules, including natural products and polymers, due to its ability to introduce allyl groups into various substrates. Additionally, it plays a role in catalytic processes and asymmetric synthesis, contributing to the development of chiral compounds used in drug discovery and material science. Its reactivity with carbonyl compounds, such as aldehydes and ketones, makes it a versatile tool in organic chemistry laboratories.
Product Specification:
| Test | Specification |
|---|---|
| CONCENTRATION | 2M |
| APPEARANCE | BROWN TO AMBER OR DARK-GREEN LIQUID |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 100.000 | 10-20 days | ฿3,960.00 |
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| 500.000 | 10-20 days | ฿12,680.00 |
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Allylmagnesium chloride
Allylmagnesium chloride is widely used in organic synthesis as a Grignard reagent, which is essential for forming carbon-carbon bonds. It is particularly valuable in the production of allylic compounds, which are important intermediates in the manufacture of pharmaceuticals, agrochemicals, and fine chemicals. The reagent is also employed in the synthesis of complex organic molecules, including natural products and polymers, due to its ability to introduce allyl groups into various substrates. Additionally, it plays a role in catalytic processes and asymmetric synthesis, contributing to the development of chiral compounds used in drug discovery and material science. Its reactivity with carbonyl compounds, such as aldehydes and ketones, makes it a versatile tool in organic chemistry laboratories.
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