2-Bromo-5-nitropyridine

2-Bromo-5-nitropyridine Basic information
Product Name:2-Bromo-5-nitropyridine
Synonyms:TIMTEC-BB SBB003519;2-BROMO-5-NITROPYRIDINE;2-BROMO-5-NITROPYRIDINE 97%;2-BROMO-5-NITROPYRIDINE 2-BROMO-5-NITROPYRIDINE;2-BORMO-5-NITROPYRIDINE;2-BroMo-5-nitropyridine, 98% 1GR;5-Nitro-2-broMopyridine;NSC 73702
CAS:4487-59-6
MF:C5H3BrN2O2
MW:202.99
EINECS:224-777-2
Product Categories:Brominated heterocyclic series;Boronic Acid;Pyridines derivates;C5Heterocyclic Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Pyridine series;Halides;Pyridine;Nucleotides and Nucleosides;Bromopyridines;Halopyridines;Bases & Related Reagents;Nucleotides;compounds of pyridine;pyridines;blocks;Bromides;NitroCompounds;pyridine derivative;Pyridines, Pyrimidines, Purines and Pteredines;Building Blocks/Intermediates
Mol File:4487-59-6.mol
2-Bromo-5-nitropyridine Structure
2-Bromo-5-nitropyridine Chemical Properties
Melting point 139-141 °C (lit.)
Boiling point 145-147 °C/10 mmHg (lit.)
density 1.8727 (rough estimate)
refractive index 1.6200 (estimate)
Fp 145-147°C/10mm
storage temp. Inert atmosphere,2-8°C
solubility Chloroform, Hot Methanol
form Crystalline Powder
pka-3.24±0.10(Predicted)
color Light yellow to light brown
Water Solubility Insoluble in water.
BRN 120901
InChIKeyHUUFTVUBFFESEN-UHFFFAOYSA-N
CAS DataBase Reference4487-59-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38-20/21/22
Safety Statements 26-37/39-22-36
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
Hazard Note Irritant/Keep Cold
HazardClass IRRITANT, IRRITANT-HARMFUL
PackingGroup III
HS Code 29333990
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
2-Bromo-5-nitropyridine Usage And Synthesis
Chemical PropertiesOff-white to light yellow crystal.
Uses2-Bromo-5-nitropyridine was used in preparation of boc-protected (piperazin-1-ylmethyl)biaryls via microwave-mediated Suzuki-Miyaura coupling with (boc-piperazin-1-ylmethyl)phenylboronic acid pinacol esters. It was also used in the synthesis of 2-pyridyl analogs. Substituted 5-nitro-2-ethynylpyridines were synthesized by the Sonogashira reaction of 2-bromo-5-5-nitropyridine with terminal acetylenes.
2,3,6-TRIBROMO-4-METHOXY-5-NITROPYRIDINE 1-Hexadecylpyridinium bromide 2,4-DIBROMO-5-NITROPYRIDINE 2-BROMO-3,5-DINITROPYRIDINE 2,6-Dibromo-3-nitropyridine 2-Amino-6-bromo-3-nitropyridine 4-Amino-2,6-dibromo-3-nitropyridine N1-(1-BROMO-4-NITRO-3-ISOQUINOLYL)BENZAMIDE 2-BROMO-5-NITROPYRIDIN-4-AMINE 2-Bromo-3-methyl-5-nitropyridine 2-BROMO-3-CHLORO-5-NITROPYRIDINE 3-Bromonitrobenzene Nitrobenzene 2-Bromo-5-nitro-4-picoline 6-BROMO-2-METHOXY-3-NITRO-PYRIDINE 2-Bromo-5-nitropyridine-1-oxide 2,3-DIBROMO-5-NITRO PYRIDINE 2-BROMO-3-IODO-5-NITROPYRIDINE

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