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Ethyl 5-bromonicotinate, 98%, Thermo Scientific Chemicals
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Catalog number B20788.14
also known as B20788-14
Price (USD)/ Each
797.00
-
Quantity:
25 g
Price (USD)/ Each
797.00
Ethyl 5-bromonicotinate, 98%, Thermo Scientific Chemicals
Catalog numberB20788.14
Price (USD)/ Each
797.00
-
Chemical Identifiers
CAS20986-40-7
IUPAC Nameethyl 5-bromopyridine-3-carboxylate
Molecular FormulaC8H8BrNO2
InChI KeyPCPIANOJERKFJI-UHFFFAOYSA-N
SMILESCCOC(=O)C1=CN=CC(Br)=C1
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Specifications
Specification Sheet
Specification SheetAssay (GC)≥97.5%
Melting Point (clear melt)37.0-44.0?C
Appearance (Color)White
FormPowder
Ethyl 5-bromonicotinate is used as a key starting material for the preparation of 5-bromonicotinic acid hydrazide via reaction with a hydrazine hydrate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Ethyl 5-bromonicotinate is used as a key starting material for the preparation of 5-bromonicotinic acid hydrazide via reaction with a hydrazine hydrate.
Notes
Incompatible with oxidizing agents.
Ethyl 5-bromonicotinate is used as a key starting material for the preparation of 5-bromonicotinic acid hydrazide via reaction with a hydrazine hydrate.
Notes
Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Houllier, N.; Lasne, M. C.; Bureau, R.; Lestage, P.; Rouden, J. Synthesis of a cytisine/epibatidine hybrid: a radical approach. Tetrahedron 2010, 66 (47), 9231-9241.
- Melzig, L.; Dennenwaldt, T.; Gavryushin, A.; Knochel, P. Direct aminoalkylation of arenes, heteroarenes, and alkenes via Ni-catalyzed Negishi cross-coupling reactions. J. Org. Chem 2011, 76 (21), 8891-8906.