40273-45-8Fc1cccnc1BrIFGLECYAEGYLSJ-UHFFFAOYSA-N40273-45-8DTXSID10376465Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Danger
H301 (10.9%): Toxic if swallowed [Danger Acute toxicity, oral]
P261, P262, P264, P264+P265, P270, P271, P280, P301+P316, P302+P352, P304+P340, P305+P351+P338, P316, P317, P319, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 46 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Verwenden2-Bromo-3-fluoropyridine is a chemical intermediate that belongs to the group of heterocyclic compounds. It is synthesized by the reaction of sodium methanethiolate and formaldehyde with magnesium. The product yield is not very high, but 2-bromo-3-fluoropyridine can be used for the synthesis of other heterocyclic compounds. The compound was first isolated in 1887 by J. Grignard from a reaction between bromine and formaldehyde. It has been shown to have formylation, nucleophilic substitution, and condensation reactions as its transition states. 2-Bromo-3-fluoropyridine can be prepared from the Grignard reagent, methanethiolate, and chlorine or magnesium chloride in an ether solution at room temperature. This compound has also been used as a reagent for the preparation of difluoromethoxybenz.
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