Hydroxybenzoic Acid Derivatives
Ambeed Bis 1 5cyclooctadiene rhodium
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate, 99326-34-8, 98+%
Ambeed Bis 1 5cyclooctadiene rhodium
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate, 99326-34-8, 98+%
Ambeed Bis 1 5cyclooctadiene rhodium
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate, 99326-34-8, 98+%
Ambeed Bis 1 5cyclooctadiene rhodium
Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate, 99326-34-8, 98+%
Medchemexpress LLC Sodium benzenesulfinate | 873-55-2 | 99.91% | 164.16 | 50 G
Sodium benzenesulfinate is a reagent employed in organic synthesis for the creation of various compounds, including sulfones. It participates in rhodium-catalyzed desulfinative coupling reactions with aldehydes, leading to the production of ketones.
- Reagent for organic synthesis.
- Used in the creation of sulfones.
- Undergoes rhodium-catalyzed desulfinative coupling with aldehydes.
- Yields ketones through specific reactions.
Medchemexpress LLC 6-Bromo-2-pyridinecarboxaldehyde | 34160-40-2 | 99.69% | C6H4BrNO | 25 G
6-Bromo-2-pyridinecarboxaldehyde is a biochemical reagent suitable for life science-related research, functioning as a biological material or organic compound. It has been utilized in studies involving rhodium-catalyzed reductive aldol coupling with divinyl ketones, which leads to syn-hydroxyenones. Additionally, it serves as a building block for Tris[(pyridyl)methyl]amine ligands.
- Biochemical reagent for life science-related research.
- Functions as a biological material or organic compound.
- Utilized in studies involving rhodium-catalyzed reductive aldol coupling.
- Serves as a building block for Tris[(pyridyl)methyl)amine ligands.
Medchemexpress LLC 6-Bromo-2-pyridinecarboxaldehyde | 34160-40-2 | 99.7% | C6H4BrNO | 10 G
6-Bromo-2-pyridinecarboxaldehyde is a biochemical reagent suitable for various life science research applications, acting as a biological material or organic compound. It is specifically utilized in the study of rhodium-catalyzed reductive aldol coupling with divinyl ketones, which results in syn-hydroxyenones. Additionally, this compound functions as a foundational building block for Tris[(pyridyl)methyl]amine ligands.
- Functions as a biological material for life science research
- Acts as an organic compound for life science research
- Utilized in rhodium-catalyzed reductive aldol coupling with divinyl ketones
- Leads to the formation of syn-hydroxyenones
- Serves as a building block for Tris[(pyridyl)methyl]amine ligands