Cyclohexylmethylmagnesium bromide manufacturers
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| | Cyclohexylmethylmagnesium bromide Basic information |
| | Cyclohexylmethylmagnesium bromide Chemical Properties |
| density | 0.966 g/mL at 25 °C | | Fp | -17 °C | | form | Solution | | color | Colorless to yellow to brown | | InChI | 1S/C7H13.BrH.Mg/c1-7-5-3-2-4-6-7;;/h7H,1-6H2;1H;/q;;+1/p-1 | | InChIKey | ZBCIOGFGZRNNEC-UHFFFAOYSA-M | | SMILES | Br[Mg]CC1CCCCC1 |
| 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 | | HazardClass | 4.3, 3 | | HS Code | 29319090 | | Storage Class | 3 - Flammable liquids | | Hazard Classifications | Acute Tox. 4 Oral
Carc. 2
Flam. Liq. 2
Skin Corr. 1B
STOT SE 3 |
| | 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 | | reaction suitability | reaction type: Grignard Reaction |
| | Cyclohexylmethylmagnesium bromide Preparation Products And Raw materials |
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