452972-09-7

452972-09-7
452972-09-7
452972-09-7

452972-09-7

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  • Min.Order :100 Kilogram
  • Purity: 99%
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452972-09-7 Supply 5-Bromopyridine-3-boronic acid CAS:452972-09-7 in China C5H5BBrNO2

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5-Bromopyridine-3-boronic acid

Product ID: JXP-06
Products5-Bromopyridine-3-boronic acid
CAS No.: 452972-09-7
Purity: 98%
Exterior: white powder
 
Stock: hectogram level standby
Production capacity : 50kg

 

5-Bromopyridine-3-boronic acid Basic information
Product Name: 5-Bromopyridine-3-boronic acid
Synonyms: 3-BROMOPYRIDYL-5-BORONIC ACID;3-BROMOPYRIDINE-5-BORONIC ACID;3-BROMO-5-PYRIDINEBORONIC ACID;3-BROMO-5-PYRIDYLBORONIC ACID;5-BROMO-3-PYRIDINEBORONIC ACID;(5-BROMO-3-PYRIDYL)BORONIC ACID;AKOS BRN-0472;5-BROMOPYRIDIN-3-YLBORONIC ACID
CAS: 452972-09-7
MF: C5H5BBrNO2
MW: 201.81
EINECS: -0
Product Categories: BORONICACID;blocks;BoronicAcids;Pyridines;Boronic acids;Halogenated;Organoborons;Pyridine;Boronic Acids;Boronic Acids and Derivatives;Heteroaryl;Boronic Acids and Derivatives;Chemical Synthesis;Heteroaryl Boronic Acids;Organometallic Reagents
Mol File: 452972-09-7.mol
5-Bromopyridine-3-boronic acid Structure
 
5-Bromopyridine-3-boronic acid Chemical Properties
mp  >300°C
storage temp.  Keep Cold
BRN  9119873
CAS DataBase Reference 452972-09-7(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
Hazard Note  Irritant/Keep Cold
HazardClass  IRRITANT
MSDS Information
Provider Language
ALFA English
 
5-Bromopyridine-3-boronic acid Usage And Synthesis
Chemical Properties white to light yellow crystal powde
Usage Reactant for preparation of:• ;Thienylpyridyl garlands via cross-coupling with heteroaryl halides1• ;Arenes via nickel-catalyzed cross-coupling with potassium aryl- and heteroaryl trifluoroborates2• ;Meso-substituted ABCD-type porphyrins by functionalization reactions3• ;Analogs of (acetylamino)(dimethylpyrazol)(pyridyl)pyrimidines as A2A adenosine receptor antagonists for the treatment of Parkinson′s disease4• ;5-hydroxy-1,3,2-dioxaborolan-4-ones boronate-amine complexes via heterocyclization with α-oxocarboxylic acids followed by subsequent complexation5&
 
5-Bromopyridine-3-boronic acid Preparation Products And Raw materials
Raw materials Diethyl ether-->n-Butyllithium-->Triisopropyl borate-->3,5-Dibromopyridine
 

 

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