Potassium 4-((morpholino)methyl)-phenyltrifluoroborate
Potassium 4-((morpholino)methyl)-phenyltrifluoroborate
CAS: 1190095-06-7
Molecular Formula: C11H14BF3KNO
Potassium 4-((morpholino)methyl)-phenyltrifluoroborate - Names and Identifiers
Potassium 4-((morpholino)methyl)-phenyltrifluoroborate - Physico-chemical Properties
| Molecular Formula | C11H14BF3KNO |
| Molar Mass | 283.1394696 |
| Storage Condition | 2-8℃ |
| Sensitive | Irritant |
| MDL | MFCD20527095 |
Potassium 4-((morpholino)methyl)-phenyltrifluoroborate - Introduction
Potassium 4-((morphinopridinyl) methyl) benzentrifluoroborate is an organic compound with the chemical formula C8H11BF3KNO. The following is a detailed description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: colorless crystal, powder substance.
-Solubility: Soluble in many organic solvents, such as dimethyl sulfoxide and acetonitrile.
-Melting point: about 150-155 degrees Celsius.
Use:
-Chemical synthesis: As the source material of benzyl-blunt-end hydrogenation agent, it can be used in chemical synthesis reactions, such as the preparation of organic boron compounds by blunt-end hydrogenation reaction.
-Ligand: It can be used as a ligand in organometallic catalytic reactions, such as Jones complex competitive catalysts.
Preparation Method:
The preparation method of potassium 4-((morphinyl) methyl) benzene trifluoroborate is more complicated, and the main steps include:
1. Benzaldehyde is reacted with sodium boron trifluoride by chemical reaction to obtain boron trifluoride benzaldehyde ester.
2. boron trifluoride benzaldehyde ester was reacted with morphine to obtain sodium 4-((morphine) methyl) benzene trifluoroborate.
3. Finally, through a simple cation exchange reaction, the sodium ion is converted into potassium ion to obtain potassium 4-((morphinyl) methyl) benzene trifluoroborate.
Safety Information:
The specific safety information of potassium 4-((morphinyl) methyl) benzene trifluoroborate may vary depending on the conditions of preparation and use. However, as a chemical, the following safety measures should be noted:
-Avoid inhalation and contact with skin. In case of skin contact, rinse immediately with plenty of water.
-Use appropriate personal protective equipment such as lab gloves, safety goggles, and lab coats when using or handling the compound.
-The compound should be stored in a dry, well-ventilated place, away from fire and oxidizing agents.
In summary, potassium 4-((morphinopyryl) methyl) benzene trifluoroborate is an organic compound commonly used as a blunt-end hydrogenation agent and ligand in chemical synthesis reactions. The preparation of the compound is complex and safe use requires attention to appropriate personal protection and storage conditions.
Nature:
-Appearance: colorless crystal, powder substance.
-Solubility: Soluble in many organic solvents, such as dimethyl sulfoxide and acetonitrile.
-Melting point: about 150-155 degrees Celsius.
Use:
-Chemical synthesis: As the source material of benzyl-blunt-end hydrogenation agent, it can be used in chemical synthesis reactions, such as the preparation of organic boron compounds by blunt-end hydrogenation reaction.
-Ligand: It can be used as a ligand in organometallic catalytic reactions, such as Jones complex competitive catalysts.
Preparation Method:
The preparation method of potassium 4-((morphinyl) methyl) benzene trifluoroborate is more complicated, and the main steps include:
1. Benzaldehyde is reacted with sodium boron trifluoride by chemical reaction to obtain boron trifluoride benzaldehyde ester.
2. boron trifluoride benzaldehyde ester was reacted with morphine to obtain sodium 4-((morphine) methyl) benzene trifluoroborate.
3. Finally, through a simple cation exchange reaction, the sodium ion is converted into potassium ion to obtain potassium 4-((morphinyl) methyl) benzene trifluoroborate.
Safety Information:
The specific safety information of potassium 4-((morphinyl) methyl) benzene trifluoroborate may vary depending on the conditions of preparation and use. However, as a chemical, the following safety measures should be noted:
-Avoid inhalation and contact with skin. In case of skin contact, rinse immediately with plenty of water.
-Use appropriate personal protective equipment such as lab gloves, safety goggles, and lab coats when using or handling the compound.
-The compound should be stored in a dry, well-ventilated place, away from fire and oxidizing agents.
In summary, potassium 4-((morphinopyryl) methyl) benzene trifluoroborate is an organic compound commonly used as a blunt-end hydrogenation agent and ligand in chemical synthesis reactions. The preparation of the compound is complex and safe use requires attention to appropriate personal protection and storage conditions.
Last Update：2024-04-10 22:29:15
