1-Bromo-2-pentyne acts as a reagent for organic and organometallic compounds. It is also employed in the preparation of stereochemically restricted lactone-type analogs of jasmonic acids, 5-oxa-7-epi-jasmonic acid and 5-oxa-jasmonic acid. Further, it is used to prepare of 4,7-decadienal, 4,7-tridecadienal, 5,8-tetradecadienal and 6,9-dodecadienal synthesis. In addition to this, it plays an important role for the synthesis of 5-ethyl-4-methylene-6-phenyl-3a,4,7,7a-tetrahydroisobenzofuran-1,3-dione.
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
1-Bromo-2-pentyne acts as a reagent for organic and organometallic compounds. It is also employed in the preparation of stereochemically restricted lactone-type analogs of jasmonic acids, 5-oxa-7-epi-jasmonic acid and 5-oxa-jasmonic acid. Further, it is used to prepare of 4,7-decadienal, 4,7-tridecadienal, 5,8-tetradecadienal and 6,9-dodecadienal synthesis. In addition to this, it plays an important role for the synthesis of 5-ethyl-4-methylene-6-phenyl-3a,4,7,7a-tetrahydroisobenzofuran-1,3-dione.
Solubility
Miscible with ether
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
Higashino, T.; Jeannin, O.; Kawamoto, T.; Lorcy, D.; Mori, T.; Fourmigue, M. A Single-Component Conductor Based on a Radical Gold Dithiolene Complex with Alkyl-Substituted Thiophene-2,3-dithiolate Ligand. Inorg. Chem. 2015, 54 (20), 9908-9913.
Aichhorn, S.; Himmelsbach, M.; Schofberger, W. Synthesis of quinoxalines or quinolin-8-amines from N-propargyl aniline derivatives employing tin and indium chlorides. Org. Biomol. Chem. 2015, 13 (36), 9373-9380.