Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Boric acid >  2-Methylpyridine-4-boronic acid

2-Methylpyridine-4-boronic acid

Basic information Safety Supplier Related

2-Methylpyridine-4-boronic acid Basic information

Product Name:
2-Methylpyridine-4-boronic acid
Synonyms:
  • 2-Methylpyridin-4-yl-4-boronic acid
  • Boronic acid, B-(2-Methyl-4-pyridinyl)-
  • 2-PICOLINE-4-BORONIC ACID
  • 2-METHYLPYRIDINE-4-BORONIC ACID
  • (2-METHYLPYRIDIN-4-YL)BORONIC ACID
  • 2-METHYL-4-PYRIDINYLBORONIC ACID
  • 2-METHYL-4-PYRIDINEBORONIC ACID
  • 2-METHYL-4-PYRIDINEBORIC ACID
CAS:
579476-63-4
MF:
C6H8BNO2
MW:
136.94
Product Categories:
  • Pyridines
  • Boronic acid
  • PYRIDINE
  • Boronic Acid series
  • Boric Acid| Boric Acid Ester| Potassium Trifluoroborate
Mol File:
579476-63-4.mol
More
Less

2-Methylpyridine-4-boronic acid Chemical Properties

Boiling point:
311.2±44.0 °C(Predicted)
Density 
1.18±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
pka
7?+-.0.10(Predicted)
form 
crystalline powder
color 
Cream
CAS DataBase Reference
579476-63-4(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
37/38-41
Safety Statements 
26-39
HazardClass 
IRRITANT
HS Code 
2933399990
More
Less

2-Methylpyridine-4-boronic acid Usage And Synthesis

Chemical Properties

white to light yellow crystal powder

Uses

suzuki reaction

Uses

(2-Methylpyridin-4-yl)boronic Acid (CAS# 579476-63-4) is used as a reagent in the preparation of dihydro-phenylquinazlinone derivatives as encephalitic alphaviruses inhibitors useful in the treatment of viral infections.

Synthesis

Under nitrogen protection, 4-bromo-2-methylpyridine, a certain proportion of tributyl borate and tetrahydrofuran were added to a four-necked flask, and the temperature was lowered to -68??-70??. Add n-butyllithium dropwise into the quartet until the solution was yellow. The solution was kept warm for 1 h. Dilute HCl was then added immediately to hydrolyze the solution. The solution first produced precipitation, with the gradual disappearance of precipitation, adjust the pH value of the system to 1. To the solution of NaOH solution with a mass fraction of 25% was added dropwise to the pH value of 13, stirring for 1 h. Separation of the liquid, the organic phase was extracted with 15 mL of NaOH with a mass fraction of 10%, and the aqueous phase was combined, and the alkaline solution was extracted with 15 mL of THF for 2 times, respectively. The obtained alkaline solution was adjusted to pH with dilute HCl, turbidity was generated at the beginning, flocculent appeared slowly, and the pH was adjusted to 5.0. The aqueous phase was extracted with 70 mL of tetrahydrofuran, and the organic phase was spin-dried and purified to obtain the product 2-methyl-4-pyridineboronic acid in 82.20% yield.

2-Methylpyridine-4-boronic acidSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
INTATRADE GmbH
Tel
+49 3493/605464
Email
sales@intatrade.de
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18934348241
Email
sales4.gd@hwrkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com