6867-35-2
Lithium tetramethanolatoborate
CAS: 6867-35-2
Molecular Formula: C4H12BLiO4
6867-35-2 - Names and Identifiers
| Name | Lithium tetramethanolatoborate |
| Synonyms | lithiuM tetraMethoxyborate Lithiumtetramethanolatoborate Lithium tetramethanolatoborate |
| CAS | 6867-35-2 |
| InChI | InChI=1/C4H12BO4.Li.H/c1-6-5(7-2,8-3)9-4;;/h1-4H3;;/q-1;;/rC4H12BO4.HLi/c1-6-5(7-2,8-3)9-4;/h1-4H3;1H/q-1 |
6867-35-2 - Physico-chemical Properties
| Molecular Formula | C4H12BLiO4 |
| Molar Mass | 141.89 |
6867-35-2 - Introduction
Lithium tetramethanolatoborate is a colorless to yellowish solid with the formula LiBO(Me)4, where Me represents a methyl group. It has good solubility, soluble in non-polar solvents such as hydrocarbons and aromatic hydrocarbons, but insoluble in water.
Lithium tetramethanolatoborate is a common organometallic compound, which is widely used in organic synthetic chemistry. It is commonly used as a ligand or catalyst precursor in organometallic chemistry. Lithium tetramethanolatoborate can be used in the Rossiter-McCollum reaction between anisole and alcohol to convert anisole to the corresponding alcohol. It can also be used in cross-coupling reactions to construct carbon-carbon bonds and hydrogen transfer reactions in organic synthesis.
A common method for preparing Lithium tetramethanolatoborate is through the reaction of tetramethanol sodium borate and lithium hydride. First, tetramethanol sodium borate and lithium hydride are mixed and reacted in a suitable environment to produce a Lithium tetramethanolatoborate.
Lithium tetramethanolatoborate have relatively low toxicity and flammability under normal use conditions. When handling it, you should take necessary safety measures, such as wearing gloves, goggles and operating in a well-ventilated place. In addition, contact with oxidants and acids should be avoided to prevent dangerous accidents. When using or storing Lithium tetramethanolatoborate, pay attention to its flammability and volatility to ensure safety.
Lithium tetramethanolatoborate is a common organometallic compound, which is widely used in organic synthetic chemistry. It is commonly used as a ligand or catalyst precursor in organometallic chemistry. Lithium tetramethanolatoborate can be used in the Rossiter-McCollum reaction between anisole and alcohol to convert anisole to the corresponding alcohol. It can also be used in cross-coupling reactions to construct carbon-carbon bonds and hydrogen transfer reactions in organic synthesis.
A common method for preparing Lithium tetramethanolatoborate is through the reaction of tetramethanol sodium borate and lithium hydride. First, tetramethanol sodium borate and lithium hydride are mixed and reacted in a suitable environment to produce a Lithium tetramethanolatoborate.
Lithium tetramethanolatoborate have relatively low toxicity and flammability under normal use conditions. When handling it, you should take necessary safety measures, such as wearing gloves, goggles and operating in a well-ventilated place. In addition, contact with oxidants and acids should be avoided to prevent dangerous accidents. When using or storing Lithium tetramethanolatoborate, pay attention to its flammability and volatility to ensure safety.
Last Update：2024-04-10 22:29:15
