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ChemicalBook Product Catalog Pharmaceutical intermediates Heterocyclic compound Pyridine compound Pyridine derivatives 3-Pyridylboronic acid

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3-Pyridylboronic acid

$ 1.00 /1KG

Min. Order1G
Purity98%
Cas No1692-25-7
Supply Ability1000KG
Update time2019-07-06

career henan chemical co

career henan chemical co

7YR

China

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Chemical Properties

Product Name	3-Pyridylboronic acid
CAS No	1692-25-7
EC-No
Min. Order	1G
Purity	98%
Supply Ability	1000KG
Release date	2019/07/06

AD68

3-Pyridylboronic acid Basic information

Product Name:	3-Pyridylboronic acid
Synonyms:	RARECHEM AH PB 0251;PYRIDIN-3-YLBORONIC ACID;PYRIDIN-3-BORONIC ACID;PYRIDIN-3-YL-3-BORONIC ACID;PYRIDYL-3-BORONIC ACID;PYRIDINE-3-BORONIC ACID;AKOS BRN-0272;3-PYRIDYLBORONIC ACID
CAS:	1692-25-7
MF:	C5H6BNO2
MW:	122.92
EINECS:	-0
Product Categories:	blocks;BoronicAcids;Pyridines;Pyridine;Boronic Acids & Esters;Boronic acids;Heterocyclic Compounds;Boronic acid;Organoborons;Aromatics Compounds;B (Classes of Boron Compounds);Boronic acid series;Aromatics;Boron Derivatives;Heterocycles;Boronic Acids & Esters;Boronic Acids;Boronic Acids and Derivatives;Heteroaryl;Boronic Acids and Derivatives;Chemical Synthesis;Heteroaryl Boronic Acids;Organometallic Reagents;OLED materials,pharm chemical,electronic;Boronate Ester;Potassium Trifluoroborate
Mol File:	1692-25-7.mol

3-Pyridylboronic acid Chemical Properties

Melting point	>300 °C(lit.)
storage temp.	0-6°C
solubility	Slightly soluble in methanol.
form	Powder, Crystals and/or Chunks
color	White to yellow-orange
BRN	471943
CAS DataBase Reference	1692-25-7(CAS DataBase Reference)

Safety Information

Hazard Codes	Xn,Xi,C,F
Risk Statements	36/37/38-22-34-11
Safety Statements	36/37/39-3-26-45-16
WGK Germany	3
Hazard Note	Irritant
HazardClass	IRRITANT, KEEP COLD

3-Pyridylboronic acid Usage And Synthesis

Chemical Properties	Light Yellow Powder
Uses	Boronic acid derivatives and their binding affinities with diols.
Uses	Reagent used for• ;Phosphine-free Suzuki-Miyaura cross-coupling reactions1 • ;Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation2 • ;N-arylation using copper acetylacetonate catalyst3 • ;Copper-mediated cyanation and regioselective cyanation of electron-rich benzenes4 Reagent use in Preparation of • ;New linear poly(phenylpyridyl) chains by Suzuki coupling5 • ;Oligopyridyl foldamers as mimics of a-helix twist6 • ;Many highly significant therapeutic enzymatic and kinase inhibitors and r
Uses	suzuki reaction

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