| Identification | Back Directory | [Name]
CYCLOHEXYLMETHYLMAGNESIUM BROMIDE | [CAS]
35166-78-0 | [Synonyms]
Bromo(cyclohexylmethyl)magnesium
CYCLOHEXYLMETHYLMAGNESIUM BROMIDE
Magnesium,bromo(cyclohexylmethyl)-
magnesium,methanidylcyclohexane,bromide
Cyclohexylmethylmagnesium bromide, 1 M in THF
(Cyclohexylmethyl)magnesium bromide solution
Cyclohexylmethylmagnesium bromide, 0.5 M in THF
Cyclohexylmethylmagnesium bromide, 0.25M solution in THF
(cyclohexylmethyl) magnesium bromide tetrahydrofuran 0.5M
Cyclohexylmethylmagnesium bromide, 0.5 m in tetrahydrofuran
Cyclohexylmethylmagnesium bromide, 0.5 M solution in THF, J&KSeal
Cyclohexylmethylmagnesium bromide, 0.25M solution in THF, AcroSeal
(CyclohexylMethyl)MagnesiuM broMide, 0.5 M solution in THF, SpcSeal | [EINECS(EC#)]
233-305-4 | [Molecular Formula]
C7H13BrMg | [MDL Number]
MFCD02260210 | [MOL File]
35166-78-0.mol | [Molecular Weight]
201.39 |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless to yellow to brown liquid | [Uses]
Reactant involved in:• ;Isomerization polymerization of alkenylcyclohexanes1• ;Intramolecular rearrangements of vinylidenecyclopropanes2• ;Cycloisomerization of cyclic and acyclic enynes3Additionally reactant involved in synthesis of biologically active molecules including:• ;Dipeptidyl boronic acid proteasome inhibitors4• ;Substituted 1,3-dihydroindole-2-ones with antitumor effects5• ;Sulfur-free transition state nucleoside analog inhibitors of methylthioadenosine nucleosidase and phosphorylase6 | [reaction suitability]
reaction type: Grignard Reaction |
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