Company Name: |
J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788 |
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jkinfo@jkchemical.com |
Products Intro: |
Product Name:4-(Isobutyramido)benzeneboronic acid 98% CAS:874219-50-8 Package:1g
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| 4-ISOBUTYRAMIDOBENZENEBORONIC ACID Basic information |
Product Name: | 4-ISOBUTYRAMIDOBENZENEBORONIC ACID | Synonyms: | [4-[(2-Methyl-1-oxopropyl)amino]phenyl]boronic acid;4-ISOBUTYRAMIDOBENZENEBORONIC ACID;4-ISOBUTYRAMIDOPHENYLBORONIC ACID;4-(Isobutyramido)benzeneboronic acid 98%;N-4-Boronophenyl isobutyramide;[4-(2-methylpropanoylamino)phenyl]boronic acid;4-(Isobutyramido)benzeneboronicacid98%;4-(Isobutyramido)benzeneboronic | CAS: | 874219-50-8 | MF: | C10H14BNO3 | MW: | 207.03 | EINECS: | | Product Categories: | Amines;blocks;BoronicAcids;Carboxes | Mol File: | 874219-50-8.mol | |
| 4-ISOBUTYRAMIDOBENZENEBORONIC ACID Chemical Properties |
Melting point | 234.8 | density | 1.16±0.1 g/cm3 (20 ºC 760 Torr) | storage temp. | Sealed in dry,2-8°C | solubility | Slightly Soluble (3.3 g/L) (25°C) | pka | 8.61±0.17(Predicted) |
Hazard Codes | Xi | Hazard Note | Irritant/Keep Cold | HS Code | 2931900090 |
| 4-ISOBUTYRAMIDOBENZENEBORONIC 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. |
| 4-ISOBUTYRAMIDOBENZENEBORONIC ACID Preparation Products And Raw materials |
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