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boron trifluoride methanol complex CAS:2802-68-8/373-57-9

Boron trifluoride methanol complex, also known as BF3·MeOH or boron trifluoride methanol adduct, is a coordination complex formed between boron trifluoride (BF3) and methanol (CH3OH). This compound is a colorless liquid with a pungent odor. It is soluble in organic solvents but immiscible in water. Boron trifluoride methanol complex finds wide use as a Lewis acid catalyst in various organic reactions, such as esterification, transesterification, and alkylation reactions.


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Application and Effect:

Boron trifluoride methanol complex has several applications due to its unique properties. Here are some key uses of this compound: Catalysis: BF3·MeOH is widely used as a Lewis acid catalyst in organic synthesis reactions. It can activate and facilitate a variety of transformations, including esterification, transesterification, and alkylation reactions. The presence of the boron trifluoride moiety enhances the reactivity and selectivity of these reactions, making it a valuable tool in synthetic chemistry. Esterification: This complex is commonly used as a catalyst in esterification reactions. It promotes the conversion of carboxylic acids and alcohols into esters, which are important compounds used in the production of fragrances, flavorings, and pharmaceuticals. BF3·MeOH facilitates the reaction by increasing the electrophilicity of the carbonyl group, thereby facilitating the nucleophilic attack of the alcohol on the acid. Transesterification: Boron trifluoride methanol complex is utilized as a catalyst in transesterification reactions. These reactions involve the exchange of ester groups between an ester and an alcohol, resulting in the formation of new esters. BF3·MeOH aids in promoting the reaction by increasing the reactivity of the starting materials and facilitating the exchange of ester groups. Alkylation Reactions: BF3·MeOH finds use as a catalyst in alkylation reactions. These reactions involve the addition of an alkyl group to a compound, typically an aromatic or olefinic substrate. The complex enhances the electrophilicity of the alkylating agent, facilitating the reaction and providing control over regioselectivity. Chemical Synthesis: This complex is used in the synthesis of various organic compounds, including pharmaceutical intermediates, specialty chemicals, and agrochemicals. BF3·MeOH aids in controlling reaction pathways, increasing yields, and improving the efficiency of the synthesis processes. Solvent and Solvation Agent: The methanol component of the complex acts as a solvent and solvation agent. It can dissolve polar and nonpolar compounds, making it useful in various chemical reactions, extractions, and chromatography techniques. The ability to solvate both organic and inorganic substances makes boron trifluoride methanol complex a versatile choice in chemical research and analysis. It is important to handle boron trifluoride methanol complex or any chemical compound with proper safety precautions. This includes wearing appropriate protective equipment, working in a well-ventilated area, and following all relevant safety guidelines and regulations.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C2H8BF3O2
Assay 99%
Appearance white powder
CAS No.  2802-68-8/373-57-9
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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