Weight | 119.244 g/mol |
---|---|
Formula | CH3BrMg |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Methylmagnesium bromide (75-16-1)
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- Factors Determining the Course and Mechanisms of Grignard Reactions. II. The Effect of Metallic Compounds on the Reaction between Isophorone and Methylmagnesium Bromide (Journal of the American Chemical Society, 1941)
- Mechanism of the Grignard Addition Reaction. VIII. Reaction Rates and Product Distribution for the Reactions of t-Butylmagnesium Chloride and Methylmagnesium Bromide with Substituted Benzophenones. (Acta Chemica Scandinavica, 1971)
- The Reduction of gem-Dibromocyclopropanes to Monobromocyclopropanes with Methylmagnesium Bromide (Journal of Organic Chemistry, 1966)
- Highly (E)-selective Wadsworth-Emmons reactions promoted by methylmagnesium bromide. (Organic Letters, 2008)
- Highly Efficient Copper(I) Iodide-Tolyl-BINAP-Catalyzed Asymmetric Conjugate Addition of Methylmagnesium Bromide to ,-Unsaturated Esters (Advanced Synthesis & Catalysis, 2008)
- Organometallic reaction mechanisms. VIII. Detailed description of the mechanism of methylmagnesium bromide addition to 2-methylbenzophenone (Journal of the American Chemical Society, 1972)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILES[CH3-].[Mg+2].[Br-]
-
InChIKeyNXPHGHWWQRMDIA-UHFFFAOYSA-M
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