Pentylmagnesium Bromide
1.0 M solution in THF,MkSeal
- Product Code: 88869
Alias:
n-pentylmagnesium bromide; pentanemagnesium bromide
CAS:
693-25-4
Molecular Weight: | 175.35 g./mol | Molecular Formula: | C₅H₁₁BrMg |
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EC Number: | MDL Number: | MFCD00000045 | |
Melting Point: | 76.5-77.5℃ | Boiling Point: | 135-137℃ (0.2 Torr) |
Density: | 0.947 g/mL at 25 °C | Storage Condition: | 2~8 ℃ |
Product Description:
Pentylmagnesium bromide is widely used in organic synthesis as a Grignard reagent. It is particularly valuable for forming carbon-carbon bonds, enabling the creation of more complex organic molecules. This reagent is commonly employed in the preparation of alcohols by reacting with carbonyl compounds such as aldehydes and ketones. Additionally, it is used in the synthesis of hydrocarbons and other organometallic compounds. Its application extends to pharmaceutical and agrochemical industries, where it aids in the production of intermediates for active ingredients. The reagent is also utilized in research laboratories for developing new synthetic pathways and studying reaction mechanisms.
Product Specification:
Test | Specification |
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CONCENTRATION | 0.9-1.1 |
APPEARANCE | GRAY LIQUID |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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100.000 | 10-20 days | ฿2,280.00 |
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500.000 | 10-20 days | ฿6,320.00 |
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1000.000 | 10-20 days | ฿11,020.00 |
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Pentylmagnesium Bromide
Pentylmagnesium bromide is widely used in organic synthesis as a Grignard reagent. It is particularly valuable for forming carbon-carbon bonds, enabling the creation of more complex organic molecules. This reagent is commonly employed in the preparation of alcohols by reacting with carbonyl compounds such as aldehydes and ketones. Additionally, it is used in the synthesis of hydrocarbons and other organometallic compounds. Its application extends to pharmaceutical and agrochemical industries, where it aids in the production of intermediates for active ingredients. The reagent is also utilized in research laboratories for developing new synthetic pathways and studying reaction mechanisms.
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