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5-Bromopyridine-3-boronic acid_Molecular_structure_CAS_452972-09-7)
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5-Bromopyridine-3-boronic acid

Catalog No. 686816 Name Sigma Aldrich
CAS Number 452972-09-7 Website http://www.sigmaaldrich.com
M. F. C5H5BBrNO2 Telephone 1-800-521-8956
M. W. 201.8137 Fax
Purity ≥95% Email
Storage Chembase ID: 12390

SYNONYMS

Title
5-溴吡啶-3-硼酸
IUPAC name
(5-bromopyridin-3-yl)boronic acid
IUPAC Traditional name
5-bromopyridin-3-ylboronic acid
Synonyms
(5-Bromo-3-pyridyl)boronic acid
(3-Bromopyridin-5-yl)boronic acid
(5-bromo-3-pyridinyl)boronic acid

DATABASE IDS

CAS Number 452972-09-7
MDL Number MFCD02685634

PROPERTIES

Empirical Formula (Hill Notation) C5H5BBrNO2
Purity ≥95%
Melting Point 260 (dec.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
General description
May contain varying amounts of anhydride.
Packaging
1, 5 g in glass bottle
Application
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
• Radioligands with optimized brain kinetics for PET imaging of nAChR6
Description (简体中文)
General description
可能含不定量的酸酐。
包装
1, 5 g in glass bottle
Application
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
• Radioligands with optimized brain kinetics for PET imaging of nAChR6

REFERENCES