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HCID 11368115Erstellt: 28. Oktober 2026

3-Bromo-2-(trifluoromethyl)pyridine

3-Bromo-2-(trifluoromethyl)pyridine · tert-butyl 4-bromo-1h-pyrazole-1-carboxylate · Halides · 3-iodo-2-piperidin-1-ylpyridine · 3-Bromo-2-trifluoromethylpyridine · 4-chloro-2-piperidin-1-ylpyridine · 4-(4-chloropyridin-2-yl)morpholine · 4-Bromo-1H-pyrazole, N1-BOC protected

https://huagongshe.com/de/chemical/11368115

Molekülstruktur von 3-Bromo-2-(trifluoromethyl)pyridine

Identifikatoren & physikalische Daten

CAS No.590371-58-7
SummenformelC6H3BrF3N
Durchschnittliche Molmasse225,99 g/mol
Monoisotopische Masse224,9401 g/mol
SMILESFC(F)(F)c1ncccc1Br
InChIKeySMZAZDGFGOHROS-UHFFFAOYSA-N
PubChem CID11368115
EC No.807-519-9
DTXSIDDTXSID70463749

Chemische & physikalische Eigenschaften

XLogP2,5
Polarare Oberfläche (TPSA)12,9
H-Brücken-Donoren0
H-Brücken-Akzeptoren4
Frei drehbare Bindungen0
Schwere Atome11
Formalladung0
Komplexität136
Schmelzpunkt34-36 °C(Solv: hexane (110-54-3))
Siedepunkt97-99 °C(Press: 35 Torr)
Dichte1.707±0.06 g/cm3(Predicted)
Lagerbedingungenunder inert gas (nitrogen or Argon) at 2-8°C
pKa (Säurekonstante)-1.80±0.22(Predicted)

Sicherheit & Vorschriften

GHS-EinstufungDangerH301 (25%): Toxic if swallowed [Danger Acute toxicity, oral]P261, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 4 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesAcute Tox. 3 (25%)
UN-TransportnummerUN2811
Zollcode2933399990
GefahrenklasseIRRITANT

Anwendungen & Verwendung

Verwenden

3-Bromo-2-(trifluoromethyl)pyridine is a fluorine-containing pyridine analogue with a bromine atom as a reactive group in its structure, which can be used in a variety of chemical reactions. It can also be used as an intermediate or raw material for organic synthesis, such as the preparation of 2-(trifluoromethyl)nicotinic acid and its derivatives.