Boron trifluoride methanol complex CAS# 2802-68-8
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Chemical Name: Boron trifluoride methanol complex
CAS No.: 2802-68-8
Molecular Formula: CH4BF3O
Molecular weight: 99.8480696
Sample: Available

Boron trifluoride methanol complex CAS# 2802-68-8: The Complete Guide
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What is Boron trifluoride methanol complex CAS# 2802-68-8?
- With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is Boron trifluoride methanol complex which has developed particularly rapidly in recent years. Do you know about Boron trifluoride methanol complex?
- The official answer: Boron trifluoride methanol complexes are adducts formed by boron trifluoride and methanol, and are often used to make boron trifluoride methanol solutions. Boron trifluoride has a colorless gas that suffocates and irritates odors, producing white smoke in the atmosphere. Boron trifluoride chemicals are soluble in cold water and concentrated sulfuric acid, acting with water to form a monohydrate or dihydrate. Boron trifluoride is one of the strongest Lewis acids, which can be combined with hydrogen fluoride, ammonia, ether, alcohols, amines, phosphines, etc. to form adducts.
What’s the application of Boron trifluoride methanol complex CAS# 2802-68-8?
Boron trifluoride-methanol complexes are used as reagents in organic chemistry because Lewis acid is a reagent used in the preparation of methyl carboxylate. It is known to be a universal building block for several other boron compounds. The ungraded products offered by TCIAmerica are generally suitable for general industrial use or research purposes, but are generally not suitable for chemicalbooks for human consumption or therapeutic use. Boron trifluoride methanol complexes are used as esterification reagents for acids and are also used for selective cleavage of triacyl ethers. Boron trifluoride – methanol complex solution can be used for the deprotection of acetylated amines of anthocyanin dyes to form a product having free amino groups. It can be used to convert sulfur-containing aminophosphate into the corresponding methyl phosphate.
Conclusion
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