2-(METHYLSULFINYL)PHENYLBORONIC ACID
2-(METHYLSULFINYL)PHENYLBORONIC ACID Basic information
- Product Name:
- 2-(METHYLSULFINYL)PHENYLBORONIC ACID
- Synonyms:
-
- 2-(METHYLSULFINYL)PHENYLBORONIC ACID
- 2-(METHYLSULPHINYL)BENZENEBORONIC ACID
- 2-(Methylsulphonyl)phenylboronicacid
- 2-(Methylsulfinyl)benzeneboronic acid, 97%
- 1-Borono-2-(methylsulphinyl)benzene
- (2-Methanesulfinylphenyl)boronic acid
- M4476G1
- Boronic acid, B-[2-(methylsulfinyl)phenyl]-
- CAS:
- 850567-97-4
- MF:
- C7H9BO3S
- MW:
- 184.02
- Product Categories:
-
- Boronate Ester
- Boronic Acid
- blocks
- BoronicAcids
- Potassium Trifluoroborate
- Mol File:
- 850567-97-4.mol
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2-(METHYLSULFINYL)PHENYLBORONIC ACID Chemical Properties
- Melting point:
- 118-122°C
- Boiling point:
- 440.5±47.0 °C(Predicted)
- Density
- 1.37±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 8.46±0.58(Predicted)
- form
- solid
- color
- white
- Water Solubility
- Slightly soluble in water.
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Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
- HazardClass
- IRRITANT
- HS Code
- 29319090
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2-(METHYLSULFINYL)PHENYLBORONIC ACID Usage And Synthesis
Uses
It is a useful intermediate in pharmaceutical intermediate. Boronic Acids are important chemical building blocks employed in cross coupling reactions. The ability of boronic acids to reversibly bind diol functional groups has been utilized for fluorescent detection of saccharides. The compound Bortezomib utilizes the boronic acid for its proteasome inhibitory effect.
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