Product

4-METHOXY-3-METHYLPHENYLBORONIC ACID

CAS No.：175883-62-2

Other grades of this product :

4-METHOXY-3-METHYLPHENYLBORONIC ACID Basic information

Product Name:	4-METHOXY-3-METHYLPHENYLBORONIC ACID
Synonyms:	AKOS BRN-0220;4-METHOXY-3-METHYLBENZENEBORONIC ACID;4-METHOXY-3-METHYLPHENYLBORONIC ACID;TIMTEC-BB SBB005903;4-Methoxy-3-methylbenzeneboronic acid 98%;m122;4-METHOXY-3-METHYLBENZENEBORONIC ACID, 98+%;1-Methoxy-2-Methylphenylboronic acid
CAS:	175883-62-2
MF:	C8H11BO3
MW:	165.98
EINECS:
Product Categories:	Aryl;Boronic Acids;blocks;BoronicAcids;Boronic Acids and Derivatives;Organoborons
Mol File:	175883-62-2.mol

4-METHOXY-3-METHYLPHENYLBORONIC ACID Chemical Properties

Melting point	205-210 °C (lit.)
Boiling point	321.4±52.0 °C(Predicted)
density	1.14±0.1 g/cm3(Predicted)
storage temp.	Keep in dark place,Sealed in dry,Room Temperature
pka	9.00±0.10(Predicted)
form	Powder
color	White to pale purple
BRN	7475212
CAS DataBase Reference	175883-62-2(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36/37/39
WGK Germany	3
HazardClass	IRRITANT
HS Code	2931900090

MSDS Information

Provider	Language
SigmaAldrich	English
ALFA	English

4-METHOXY-3-METHYLPHENYLBORONIC ACID Usage And Synthesis

Uses

suzuki reaction

Uses

Reactant for:

Preparation of hydroxyphenylnaphthols as 17β-hydroxysteroid dehydrogenase Type 2 inhibitors
Synthesis of bioactive combretastatin analogs via regioselective Suzuki coupling
Preparation of aromatic nitriles via copper-mediated cyanation
Rhodium-catalyzed allylic arylation of meso cyclopentene dicarbonates
Lewis acid-assisted asymmetric allylic substitution of butenediyl carbonates using rhodium catalyst

4-METHOXY-3-METHYLPHENYLBORONIC ACID Preparation Products And Raw materials

Raw materials

4-METHOXY-3-METHYLPHENYLMAGNESIUM BROMIDE-->4-BROMO-2-METHYLANISOLE-->Triisopropyl borate

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