CYCLOHEXYLMETHYLMAGNESIUM BROMIDE

CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Basic information
Product Name:CYCLOHEXYLMETHYLMAGNESIUM BROMIDE
Synonyms:Cyclohexylmethylmagnesium bromide, 0.5 M in THF;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
CAS:35166-78-0
MF:C7H13BrMg
MW:201.39
EINECS:
Product Categories:Grignard Reagents;Organometallic Reagents;Alkyl;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
form Solution
color Colorless to yellow to brown
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
WGK Germany 3
HS Code 29319090
MSDS Information
CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Usage And Synthesis
Chemical PropertiesColorless to yellow to brown liquid
UsesReactant involved in:
  • Isomerization polymerization of alkenylcyclohexanes
  • Intramolecular rearrangements of vinylidenecyclopropanes
  • Cycloisomerization of cyclic and acyclic enynes

Additionally reactant involved in synthesis of biologically active molecules including:
  • Dipeptidyl boronic acid proteasome inhibitors
  • Substituted 1,3-dihydroindole-2-ones with antitumor effects
  • Sulfur-free transition state nucleoside analog inhibitors of methylthioadenosine nucleosidase and phosphorylase
UsesReactant 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
CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Preparation Products And Raw materials
1,1-DIMETHYLPROPYLMAGNESIUM CHLORIDE 3-FLUORO-2-METHYLPHENYLMAGNESIUM BROMID& (2-(1-PIPERIDINYLMETHYL)PHENYL)MAGNESIU& Tetrahydropyran-4-ylmagnesium chloride, 0.50 M in THF 3-Methylbut-2-enylmagnesium chloride, 0.50 M in THF METHYLLITHIUM LITHIUM BROMIDE COMPLEX (1,3-DIOXAN-2-YLETHYL)MAGNESIUM BROMIDE (2-ETHYLHEXYL)MAGNESIUM BROMIDE 1M SOL& (3-(1-PIPERIDINYLMETHYL)PHENYL)MAGNESIU& 4-METHOXYBENZYLMAGNESIUM CHLORIDE Pyridin-3-ylmagnesium bromide (4-(1-PIPERIDINYLMETHYL)PHENYL)MAGNESIU& 2-ETHYLBUTYLMAGNESIUM BROMIDE CYCLOHEXYLMETHYLMAGNESIUM BROMIDE N-BUTYLMAGNESIUM BROMIDE ISOBUTYLMAGNESIUM BROMIDE N-PROPYLMAGNESIUM BROMIDE HEPTYLMAGNESIUM BROMIDE

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.