68003-52-1
hydrogen (butyrato-O)trifluoroborate(1-)
CAS: 68003-52-1
Molecular Formula: C4H8BF3O2
68003-52-1 - Names and Identifiers
| Name | hydrogen (butyrato-O)trifluoroborate(1-) |
| Synonyms | hydrogen (butyrato-O)trifluoroborate(1-) |
| CAS | 68003-52-1 |
| EINECS | 268-133-9 |
68003-52-1 - Physico-chemical Properties
| Molecular Formula | C4H8BF3O2 |
| Molar Mass | 155.91 |
68003-52-1 - Introduction
butyrato-O (hydrogen) trifluoroborate(1-)(hydrogen (but acid ester-O)trifluoroborate ion) is an organic compound with the molecular formula C4H6BF3O2. The following is an introduction to some of its properties, uses, methods and safety information:
Nature:
-Hydrogen (but acid ester-O) trifluoroborate ion is an ionic compound with a negative charge.
-Its appearance is colorless to light yellow solid or crystal form.
-It is solid at room temperature and is a compound soluble in some organic solvents.
-Hydrogen (but acid ester-O) trifluoroborate ion is relatively stable in the air, but may react when thermally decomposed or in the presence of organic acids.
Use:
-hydrogen (but acid ester-O) trifluoroborate ion is widely used in organic synthesis reactions and is an important reagent in organometallic chemistry.
-It is often used as an Organoboron in ligands or catalysts to easily transfer functional groups, such as Allier reactions and substitution reactions.
Preparation Method:
-hydrogen (but acid ester-O) trifluoroborate ion is usually prepared by reacting trifluoroboric acid with the corresponding ester (such as butyrate).
-In the laboratory, generally under ice bath conditions, dissolve trifluoroboric acid in an appropriate amount of organic solvent, and then slowly add the corresponding Ester, the reaction was stirred at constant temperature for several hours.
Safety Information:
-Hydrogen (but acid ester-O) trifluoroborate ion compounds are usually relatively safe under normal use conditions.
-However, because it is a chemical substance, it must follow laboratory safety procedures and wear appropriate protective equipment when using it.
-If inhaled, in contact with skin or ingested, seek immediate medical help with detailed information about the compound.
-This compound should avoid contact with strong oxidants or strong acids in view of its characteristics of organic fluorine compounds to prevent dangerous situations.
Nature:
-Hydrogen (but acid ester-O) trifluoroborate ion is an ionic compound with a negative charge.
-Its appearance is colorless to light yellow solid or crystal form.
-It is solid at room temperature and is a compound soluble in some organic solvents.
-Hydrogen (but acid ester-O) trifluoroborate ion is relatively stable in the air, but may react when thermally decomposed or in the presence of organic acids.
Use:
-hydrogen (but acid ester-O) trifluoroborate ion is widely used in organic synthesis reactions and is an important reagent in organometallic chemistry.
-It is often used as an Organoboron in ligands or catalysts to easily transfer functional groups, such as Allier reactions and substitution reactions.
Preparation Method:
-hydrogen (but acid ester-O) trifluoroborate ion is usually prepared by reacting trifluoroboric acid with the corresponding ester (such as butyrate).
-In the laboratory, generally under ice bath conditions, dissolve trifluoroboric acid in an appropriate amount of organic solvent, and then slowly add the corresponding Ester, the reaction was stirred at constant temperature for several hours.
Safety Information:
-Hydrogen (but acid ester-O) trifluoroborate ion compounds are usually relatively safe under normal use conditions.
-However, because it is a chemical substance, it must follow laboratory safety procedures and wear appropriate protective equipment when using it.
-If inhaled, in contact with skin or ingested, seek immediate medical help with detailed information about the compound.
-This compound should avoid contact with strong oxidants or strong acids in view of its characteristics of organic fluorine compounds to prevent dangerous situations.
Last Update：2024-04-10 22:29:15
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