Bromo(cyclohexylmethyl)magnesium
(Cyclohexylmethyl)magnesium bromide
CAS: 35166-78-0
Molecular Formula: C7H13BrMg
Bromo(cyclohexylmethyl)magnesium - Names and Identifiers
Bromo(cyclohexylmethyl)magnesium - Physico-chemical Properties
| Molecular Formula | C7H13BrMg |
| Molar Mass | 201.39 |
| Density | 0.966 g/mL at 25 °C |
| Flash Point | -17°C |
| Appearance | Solution |
| Color | Colorless to yellow to brown |
Bromo(cyclohexylmethyl)magnesium - Risk and Safety
| Risk Codes | R11 - Highly Flammable R14 - Reacts violently with water R19 - May form explosive peroxides R34 - Causes burns R37 - Irritating to the respiratory system R40 - Limited evidence of a carcinogenic effect |
| Safety Description | S16 - Keep away from sources of ignition. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | UN 2924 3/PG 2 |
| WGK Germany | 3 |
| HS Code | 29319090 |
Bromo(cyclohexylmethyl)magnesium - Introduction
Cyclohexylmethylmagnesium bromide is an organic compound with the chemical formula C8H15BrMg. It is a colorless to yellow liquid, usually in the form of a solution. The following is a description of some of the properties, uses, preparation and safety information of cyclohexyl methyl magnesium bromide:
Nature:
-Cyclohexylmethyl magnesium bromide is an alkyl bromide. It is a stable compound and can be stored for a long time at room temperature.
-It can react with many organic compounds and is usually used as an active reagent in organic synthesis.
-Cyclohexylmethylmagnesium bromide has good nucleophilicity and can react with many electron-deficient compounds.
Use:
-Cyclohexyl methyl magnesium bromide is widely used in organic synthesis. It can be used as a reagent for the synthesis of organic compounds such as alcohols, ethers, ketones, acids, anhydrides and ketones, and is commonly used in the synthesis of macromolecules, the synthesis of natural products and the synthesis of drugs.
-It can also be used for catalyst preparation.
Preparation Method:
-Cyclohexylmethyl magnesium bromide is generally prepared by reacting magnesium bromide with cyclohexylmethyl halide. Specific methods can refer to the organic synthetic chemistry handbook or literature.
Safety Information:
-Cyclohexyl methyl magnesium bromide has certain toxicity to the human body, and direct contact with skin and inhalation of its vapor should be avoided.
-Wear protective gloves, glasses and lab coat when using, and ensure that the operation is carried out in a well-ventilated place.
-Follow proper handling and storage of chemicals.
Nature:
-Cyclohexylmethyl magnesium bromide is an alkyl bromide. It is a stable compound and can be stored for a long time at room temperature.
-It can react with many organic compounds and is usually used as an active reagent in organic synthesis.
-Cyclohexylmethylmagnesium bromide has good nucleophilicity and can react with many electron-deficient compounds.
Use:
-Cyclohexyl methyl magnesium bromide is widely used in organic synthesis. It can be used as a reagent for the synthesis of organic compounds such as alcohols, ethers, ketones, acids, anhydrides and ketones, and is commonly used in the synthesis of macromolecules, the synthesis of natural products and the synthesis of drugs.
-It can also be used for catalyst preparation.
Preparation Method:
-Cyclohexylmethyl magnesium bromide is generally prepared by reacting magnesium bromide with cyclohexylmethyl halide. Specific methods can refer to the organic synthetic chemistry handbook or literature.
Safety Information:
-Cyclohexyl methyl magnesium bromide has certain toxicity to the human body, and direct contact with skin and inhalation of its vapor should be avoided.
-Wear protective gloves, glasses and lab coat when using, and ensure that the operation is carried out in a well-ventilated place.
-Follow proper handling and storage of chemicals.
Last Update：2024-04-09 02:00:49
