3,5-Dibromopyridine
3,5-Dibromopyridine
  • CAS No.:625-92-3
Other grades of this product :
3,5-Dibromopyridine Basic information
Product Name:3,5-Dibromopyridine
Synonyms:3,5-DIBROMOPYRIDINE;IFLAB-BB F1995-0190;3,5-Dibromopyridine,99%;3,5-Dibromopyridine, 98+%;3,5-dibormopyridine;3,5-DibroMopyridine, 97+%;3, 5-2 broMide pyridine;3,5-Dibromopyridine 99%
CAS:625-92-3
MF:C5H3Br2N
MW:236.89
EINECS:210-916-4
Product Categories:Halogenated Heterocycles;Heterocyclic Building Blocks;C5Heterocyclic Building Blocks;Brominated heterocyclic series;Boronate Ester;Boronic Acid;Pyridines derivates;API intermediates;Halogenated;Organohalides;Aromatics Compounds;Bromopyridines;Halopyridines;Potassium Trifluoroborate;blocks;Bromides;Pyridines;Pyridine;Pyridines, Pyrimidines, Purines and Pteredines;Aromatics;Bases & Related Reagents;Nucleotides;bc0001
Mol File:625-92-3.mol
3,5-Dibromopyridine Chemical Properties
Melting point 110-115 °C (lit.)
Boiling point 222 °C
density 2.0383 (rough estimate)
refractive index 1.5800 (estimate)
storage temp. Inert atmosphere,Room Temperature
solubility DMSO (Slightly, Heated), Methanol (Slightly)
pka0.52±0.20(Predicted)
form Needle-Like Crystals
color White to light beige
Water Solubility Soluble in Chloroform and Methanol. Insoluble in water.
BRN 108477
InChIKeySOSPMXMEOFGPIM-UHFFFAOYSA-N
CAS DataBase Reference625-92-3(CAS DataBase Reference)
NIST Chemistry Reference3,5-Dibromopyridine(625-92-3)
EPA Substance Registry System3,5-Dibromopyridine (625-92-3)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/21/22
Safety Statements 26-36-36/37/39
RIDADR UN2811
WGK Germany 3
HazardClass IRRITANT
HS Code 29333999
MSDS Information
ProviderLanguage
3,5-Dibromopyridine English
ACROS English
SigmaAldrich English
ALFA English
3,5-Dibromopyridine Usage And Synthesis
Chemical PropertiesLight-Yellow Solid
Uses3-Acetylamino-5-ethoxypyridine was prepared by converting 3, 5-dibromopyridine with sodium ethylate into 3-bromo-5-ethoxypyridine, allowing this substance to interact with ammonia and acetylating the aminoethoxypyridine thus formed with acetic anhydride. Lithiation of 3, 5-dibromopyridine with LDA and subsequent reaction with electrophiles provided 4-alkyl-3, 5-dibromopyridines 2 in high yield. Ligand was prepared by a Pd(0)-catalyzed cross-coupling reaction of 3,5-dibromopyridine and 5-tributylstannyl-3,3?-bipyridine. The synthesis of 3, 5-bis (2-indolyl) pyridine and 3-[(2-indolyl)-5-phenyl] pyridine derivatives as includes Stille or Suzuki type reactions, which were realized on the 3,5-dibromopyridine.
General Description3,5-Dibromopyridine undergoes lithiation with lithium diisopropylamide and on subsequent reaction with electrophiles yields 4-alkyl-3,5-dibromopyridines.

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