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- (R)-Methyl Oxazaborolidine
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- (R)-(+)-1-Phenylethanol
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- (R)-1-(3,5-Bis-trifluoromethylphenyl)ethanol
- (S)-1-(3,5-Bis-trifluoromethylphenyl)ethanol
- (1R,2R,3S,5R)-(-)-2,3-Pinanediol
- (1S,2S,3R,5S)-(+)-2,3-Pinanediol
- (1S,2S,5S)-(-)-2-Hydroxy-3-pinanone
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- (R)-Styrene oxide
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- (R)-(3-Chlorophenyl)oxirane
- (R)-(4-Fluorophenyl)oxirane
- (R)-(+)-1-(1-Naphthyl)ethanol
- (S)-(−)-1-(1-Naphthyl)ethanol
- Others
- Methylindole
- 2,4-Dichloropyrimidine
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Methyl boronic acid
【Catalog Number】BA5451
【CAS #】 13061-96-6
【Molecular Formula】CH5O2B
【Molecular Weight】59.86
|
Alias |
Boric Acid; Methyl Boron Hydroxide |
|
Catalog Number |
BA5451 |
|
CAS # |
13061-96-6 |
|
Molecular Formula |
CH5O2B |
|
Molecular Weight |
59.86 |
|
Structural Formula |
|
|
Product Introduction CAS 13061-96-6 |
Methylboronic acid, the English name is Methylboronic acid, and the American Chemical Abstracts Registry Number is cas 13061-96-6. Methylboronic acid (cas 13061-96-6) is used as an organic synthesis reagent. It can form cyclic borate with diol or diamine. Cis and trans cyclic diols form boric acid esters with different ratios of boric acid. This property can be used to separate cis and trans diols. Cross-coupling reaction with halogenated aromatics and halogenated olefins under the action of catalysts. Used as a protecting group for diols or diamines. This type of boric acid reacts easily with both and leaves easily. The protecting group is relatively stable in reactions such as esterification, methylation and silylation of hydroxyl groups. |
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