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Magnesium,bromo(cyclohexylmethyl)- 98.0% 35166-78-0
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CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Basic information
Product Name: CYCLOHEXYLMETHYLMAGNESIUM BROMIDE
Synonyms: CYCLOHEXYLMETHYLMAGNESIUM BROMIDE;(Cyclohexylmethyl)magnesium bromide solution;Cyclohexylmethylmagnesium bromide, 0.25M solution in THF, AcroSeal;Bromo(cyclohexylmethyl)magnesium;(CyclohexylMethyl)MagnesiuM broMide, 0.5 M solution in THF, SpcSeal;Magnesium,bromo(cyclohexylmethyl)-;(cyclohexylmethyl) magnesium bromide tetrahydrofuran 0.5M
CAS: 35166-78-0
MF: C7H13BrMg
MW: 201.39
EINECS:
Product Categories: Alkyl;Grignard Reagents;Organometallic Reagents;Chemical Synthesis;Grignard Reagents;Organometallic Reagents
Mol File: 35166-78-0.mol
CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Structure
CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Chemical Properties
density 0.966 g/mL at 25 °C
Fp -17 °C
Safety Information
Hazard Codes F,C
Risk Statements 11-14-19-34-37-40
Safety Statements 16-26-36/37/39-45
RIDADR UN 2924 3/PG 2
MSDS Information
CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Usage And Synthesis
Chemical Properties Colorless to yellow to brown liquid
Usage 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
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