4-Methyl-3-nitrophenylboronic acid

4-Methyl-3-nitrophenylboronic acid Basic information

Product Name:	4-Methyl-3-nitrophenylboronic acid
Synonyms:	Boronic acid,B-(4-Methyl-3-nitrophenyl)-;B-(4-Methyl-3-nitrophenyl)boronic acid;RARECHEM AH PB 0107;3-NITRO-P-TOLYLBORONIC ACID;4-METHYL-3-NITROPHENYLBORONIC ACID;4-METHYL-3-NITROBENZENEBORONIC ACID;AKOS BRN-0124;4-Methyl-3-nitrophenylboronic acid~3-Nitro-p-tolylboronic acid
CAS:	80500-27-2
MF:	C7H8BNO4
MW:	180.95
EINECS:	672-692-8
Product Categories:	Heterocyclic Compounds;Boronic Acid;blocks;BoronicAcids;NitroCompounds;Aryl;Boronic Acids;Boronic Acids and Derivatives;B (Classes of Boron Compounds);Boronic Acids;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Disubstituted Aryl Boronic Acids;Organometallic Reagents
Mol File:	80500-27-2.mol

4-Methyl-3-nitrophenylboronic acid Chemical Properties

Melting point	265-270 °C (lit.)
Boiling point	356.7±52.0 °C(Predicted)
density	1.33±0.1 g/cm3(Predicted)
storage temp.	under inert gas (nitrogen or Argon) at 2-8°C
solubility	soluble in Methanol,Acetone
pka	7.19±0.10(Predicted)
form	powder to crystal
color	White to Light yellow to Light orange
BRN	3279018
CAS DataBase Reference	80500-27-2(CAS DataBase Reference)

Safety Information

MSDS Information

Provider	Language
SigmaAldrich	English
ALFA	English

4-Methyl-3-nitrophenylboronic acid Usage And Synthesis

Chemical Properties	white to light yellow crystal powder
Uses	Reactant for: Preparation of inhibitors of lactate dehydrogenase against cancer cell proliferation Suzuki-Miyaura coupling reactions Preparation of imidazothiazoles as iodide efflux inhibitors in thyrocytes
Uses	Reactant for:• ;Preparation of inhibitors of lactate dehydrogenase against cancer cell proliferation1• ;Suzuki-Miyaura coupling reactions2,3• ;Preparation of imidazothiazoles as iodide efflux inhibitors in thyrocytes4

4-Methyl-3-nitrophenylboronic acid Preparation Products And Raw materials

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