CYCLOHEXYLMETHYLMAGNESIUM BROMIDE
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CYCLOHEXYLMETHYLMAGNESIUM BROMIDE
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CAS No:
35166-78-0
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Formula:
C7H13BrMg
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Chemical Name:
CYCLOHEXYLMETHYLMAGNESIUM BROMIDE
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Synonyms:
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;magnesium,methanidylcyclohexane,bromide;CYCLOHEXYLMETHYLMAGNESIUM BROMIDE;(Cyclohexylmethyl)magnesiumbromidesolution
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CAS No:
Safety Information
UN29243/PG2
3
11-14-19-34-37-40
16-26-36/37/39-45
F,C
P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, P501
H314
|Danger|H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501|Aggregated GHS information provided by 39 companies from 2 notifications to the ECHA C&L Inventory.
CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Use and Manufacturing
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
Computed Properties
Molecular Weight:201.39
Hydrogen Bond Acceptor Count:2
Exact Mass:200.00510
Monoisotopic Mass:200.00510
Heavy Atom Count:9
Complexity:50.9
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes
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CYCLOHEXYLMETHYLMAGNESIUM BROMIDE
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