ChemicalBook > Product Catalog > Organic Chemistry > Organometallic compounds > Organomagnesium > CYCLOHEXYLMETHYLMAGNESIUM BROMIDE
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:
- 233-305-4
- Product Categories:
-
- Grignard Reagents
- Organometallic Reagents
- Alkyl
- Chemical Synthesis
- Grignard Reagents
- Organometallic Reagents
- Mol File:
- 35166-78-0.mol
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CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Chemical Properties
- Density
- 0.966 g/mL at 25 °C
- Flash point:
- -17 °C
- form
- Solution
- color
- Colorless to yellow to brown
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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
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CYCLOHEXYLMETHYLMAGNESIUM BROMIDE Usage And Synthesis
Chemical Properties
Colorless to yellow to brown liquid
Uses
Reactant 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
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
CYCLOHEXYLMETHYLMAGNESIUM BROMIDESupplier
J & K SCIENTIFIC LTD.
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
- Tel
- 021-61259108 18621169109
- market03@meryer.com
Beijing Ouhe Technology Co., Ltd
- Tel
- 010-82967028 13552068683
- 2355560935@qq.com
Shanghai Hanhong Scientific Co.,Ltd.
- Tel
- 021-54306202 13764082696
- info@hanhongsci.com
Shandong Xiya Chemical Co., Ltd
- Tel
- 4009903999 13355009207
- 3007715519@qq.com
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CYCLOHEXYLMETHYLMAGNESIUM BROMIDE(35166-78-0)Related Product Information
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- 4-METHOXYBENZYLMAGNESIUM CHLORIDE
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- (2-ETHYLHEXYL)MAGNESIUM BROMIDE 1M SOL&
- (1,3-DIOXAN-2-YLETHYL)MAGNESIUM BROMIDE
- METHYLLITHIUM LITHIUM BROMIDE COMPLEX
- 3-Methylbut-2-enylmagnesium chloride, 0.50 M in THF
- Tetrahydropyran-4-ylmagnesium chloride, 0.50 M in THF
- (2-(1-PIPERIDINYLMETHYL)PHENYL)MAGNESIU&
- 3-FLUORO-2-METHYLPHENYLMAGNESIUM BROMID&
- 1,1-DIMETHYLPROPYLMAGNESIUM CHLORIDE
- N-BUTYLMAGNESIUM BROMIDE
- HEPTYLMAGNESIUM BROMIDE
- N-PROPYLMAGNESIUM BROMIDE
- ISOBUTYLMAGNESIUM BROMIDE
- 2-ETHYLBUTYLMAGNESIUM BROMIDE
- CYCLOHEXYLMETHYLMAGNESIUM BROMIDE