Ethynylmagnesium bromide
0.5 M solution in THF, MkSeal
- Product Code: 88902
CAS:
4301-14-8
| Molecular Weight: | 129.24 g./mol | Molecular Formula: | C₂HBrMg |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075342 | |
| Melting Point: | Boiling Point: | ||
| Density: | 0.94 g/mL at 25 °C | Storage Condition: | 2~8 ℃ |
Product Description:
Ethynylmagnesium bromide is widely used in organic synthesis as a Grignard reagent. It is particularly valuable for introducing the ethynyl group (C≡CH) into various organic molecules, enabling the formation of carbon-carbon bonds. This reagent is commonly employed in the synthesis of alkynes, which are essential intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is utilized in the preparation of complex organic compounds, including natural products and polymers, where the ethynyl group serves as a key functional moiety. Its reactivity with carbonyl compounds, such as aldehydes and ketones, makes it a versatile tool for constructing alcohols and other derivatives with high precision.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Yellow to Orange or Brown to Black liquid |
| Assayas active BuLi | 0.5 M |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 100.000 | 10-20 days | ฿1,980.00 |
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| 500.000 | 10-20 days | ฿5,080.00 |
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| 1000.000 | 10-20 days | ฿8,820.00 |
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Ethynylmagnesium bromide
Ethynylmagnesium bromide is widely used in organic synthesis as a Grignard reagent. It is particularly valuable for introducing the ethynyl group (C≡CH) into various organic molecules, enabling the formation of carbon-carbon bonds. This reagent is commonly employed in the synthesis of alkynes, which are essential intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is utilized in the preparation of complex organic compounds, including natural products and polymers, where the ethynyl group serves as a key functional moiety. Its reactivity with carbonyl compounds, such as aldehydes and ketones, makes it a versatile tool for constructing alcohols and other derivatives with high precision.
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