Brofaromine

Other Notes Use as chiral building block Debromo-silylation and -phosphonylation

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application 1-Bromo-1-propene upon n -BuLi treatment generates the propynyllithium anion, in situ , which later undergoes nucleophilic addition reactions. Some of its other applications are: Synthesis of organic reagents such as methyl but-2-ynoate

Application Isobutyl bromide has been used in a reaction with 1-ethylimidazole in a 140 °C oil bath to yield 97% 1-ethyl-1,3-isobutylimidazolium bromide.

Application Isobutyl bromide has been used in a reaction with 1-ethylimidazole in a 140 °C oil bath to yield 97% 1-ethyl-1,3-isobutylimidazolium bromide.

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 1.

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 1.

CH₃(CH₂)₄C&equivCCH₂Br CAS#: 18495-27-7 F.W.: 189.10 Requires refrigeration.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.