Halophenols
Medchemexpress LLC Rhodium(II) triphenylacetate dimer | 142214-04-8 | MFCD15071082 | 1355.14 | C80H60O8Rh2 | 1 G
Rhodium(II) triphenylacetate dimer is a dirhodium(II) carboxylate complex used as a catalyst in organic synthesis and biochemical research. The complex contains two rhodium centers bridged by four triphenylacetate ligands and is commonly applied in carbene-transfer, C-H insertion, and related transformations. Handle under inert gas and protect from light.
Medchemexpress LLC Rhodium(II) triphenylacetate dimer | 142214-04-8 | MFCD15071082 | 1355.14 | C80H60O8Rh2 | 25 MG
Rhodium(II) triphenylacetate dimer is a dimeric rhodium complex used as a catalyst in organic synthesis, notably for C-H activation and carbene-transfer reactions. It is supplied as a light-sensitive solid and should be protected from light and stored under inert atmosphere at low temperature for optimal stability.
- Catalyzes C-H activation and carbene-transfer reactions with high selectivity.
- Improves reaction rates and selectivity in complex molecule construction.
- Provided as a light-sensitive solid; protect from light during handling and storage.
- Maintain under inert atmosphere and low temperature for long-term stability.
- Suitable for research use and synthetic methodology development.
Medchemexpress LLC Rhodium(II) triphenylacetate dimer | 142214-04-8 | MFCD16875675 | 1355.14 | C80H60O8Rh2 | 50 MG
Rhodium(II) triphenylacetate dimer is a dirhodium carboxylate complex used as a homogeneous catalyst in organic synthesis. It is commonly employed for C-H activation, carbene transfer, and cyclopropanation reactions, and is supplied for research-scale applications.
- Efficient catalyst for C-H activation and insertion reactions.
- High selectivity and reaction rate in typical catalytic transformations.
- Useful for cyclopropanation and carbene-transfer methodologies.
- Suitable for small-scale research and method development.
- Provided as a solid reagent compatible with common organic solvents.
Medchemexpress LLC Rhodium(II) triphenylacetate dimer | 142214-04-8 | MFCD15071082 | 1355.14 | C80H60O8Rh2 | 250 MG
Rhodium(II) triphenylacetate dimer is a dirhodium(II) carboxylate complex used as a homogeneous catalyst in organic synthesis. It promotes C-H activation and related transformations, helping to construct complex and biologically active molecules by improving reaction rates and selectivity.
- Catalyzes C-H activation and related functionalization reactions.
- Improves reaction rate and selectivity in complex molecule synthesis.
- Dirhodium(II) carboxylate structure suited for homogeneous catalysis.
- Available in multiple package sizes for bench-scale experiments.
Medchemexpress LLC Rhodium(II) triphenylacetate dimer | 142214-04-8 | MFCD15071082 | >95.0% | 1355.14 | C80H60O8Rh2 | 10 MG
Rhodium(II) triphenylacetate dimer is a dirhodium(II) carboxylate complex used as a catalyst and reagent in organic synthesis and biochemical research (CAS 142214-04-8). It is supplied as a solid, typically colorless to light green, and is used in carbene transfer, C-H insertion, and related catalytic transformations. Purity documentation is available from the supplier.
- Dirhodium metal complex suited for catalytic applications in organic synthesis.
- Facilitates carbene transfer and C-H insertion reactions.
- Supplied as a solid with colorless to light green appearance for laboratory use.
- Offered in multiple small-scale quantities to support research workflows.
- Documentation and purity information available upon request for quality control.
Medchemexpress LLC Rhodium(II) triphenylacetate dimer | 142214-04-8 | MFCD15071082 | 1355.14 g/mol | C80H60O8Rh2 | 100 MG
Rhodium(II) triphenylacetate dimer is a dirhodium catalyst used in organic synthesis to promote C-H activation, cyclopropanation, and related transformations. Supplied as a solid for laboratory research, it is employed in small-scale catalytic screening and preparative reactions where selective C-H insertion and high reaction rates are required.
- High catalytic activity for C-H activation and insertion reactions.
- Useful for cyclopropanation and construction of complex molecules.
- Supplied as a solid, colorless to light green, suitable for laboratory use.
- Store protected from light and under inert gas to maintain stability.
- Accompanied by technical documentation and safety data for handling.
Medchemexpress LLC Rhodium(II) triphenylacetate dimer | 142214-04-8 | MFCD15071082 | >=97.0% | 1355.14 g/mol | C80H60O8Rh2 | 500 MG
Rhodium(II) triphenylacetate dimer is a dimeric rhodium catalyst widely used in organic synthesis for C-H activation and related metal-catalyzed transformations. Supplied as a solid, it exhibits high selectivity and promotes efficient formation of carbon-carbon and carbon-heteroatom bonds; store protected from light and under inert atmosphere to maintain activity.
- Dimeric rhodium catalyst for C-H activation and carbene-transfer reactions.
- High selectivity and reaction rate in catalytic transformations.
- Solid form with recommended storage to preserve activity.
- Suitable for method development and scale-up in organic synthesis.
- Characterized and documented for reproducible results.
Medchemexpress LLC Sodium benzenesulfinate | 873-55-2 | 99.97% | 164.16 | 1 ML
Sodium benzenesulfinate is a reagent utilized in organic synthesis for the creation of other compounds, such as sulfones. It undergoes rhodium-catalyzed desulfinative coupling with aldehydes to produce ketones.
- Reagent used in organic synthesis to create compounds like sulfones.
- Undergoes rhodium-catalyzed desulfinative coupling with aldehydes to yield ketones.
Medchemexpress LLC Benzenesulfinic acid, sodium salt (1:1) | 873-55-2 | 99.97% | 164.16 | 25 G
Sodium benzenesulfinate is a reagent employed in organic synthesis for the creation of other compounds, such as sulfones. It participates in rhodium-catalyzed desulfinative coupling reactions with aldehydes, resulting in the production of ketones.
- Reagent for organic synthesis
- Used to create sulfones
- Undergoes rhodium-catalyzed desulfinative coupling with aldehydes to yield ketones
Medchemexpress LLC Benzenesulfinic acid, sodium salt (1:1) | 873-55-2 | 99.97% | 164.16 | 250 G
Sodium benzenesulfinate is a reagent used in organic synthesis to create other compounds, such as sulfones. It undergoes rhodium-catalyzed desulfinative coupling with aldehydes to yield ketones.
- Reagent for organic synthesis
- Used to create sulfones
- Facilitates rhodium-catalyzed desulfinative coupling with aldehydes
- Yields ketones
Medchemexpress LLC Sodium benzenesulfinate | 873-55-2 | 99.91% | 164.16 | 100 G
Sodium benzenesulfinate is a reagent utilized in organic synthesis for creating various compounds, including sulfones. It participates in rhodium-catalyzed desulfinative coupling reactions with aldehydes, resulting in the formation of ketones.
- Functions as a versatile reagent in organic synthesis.
- Facilitates the creation of sulfones.
- Participates in rhodium-catalyzed desulfinative coupling reactions.
- Enables the synthesis of ketones from aldehydes.
Medchemexpress LLC Sodium benzenesulfinate | 873-55-2 | 99.9% | 164.16 | 500 G
Sodium benzenesulfinate is a reagent used in organic synthesis to create other compounds, such as sulfones. It undergoes rhodium-catalyzed desulfinative coupling with aldehydes to yield ketones. This product is a solid, white to off-white in appearance.
- Used in organic synthesis
- Undergoes rhodium-catalyzed desulfinative coupling
- Available as a solid
- White to off-white color
- Stable under recommended storage conditions
- Incompatible with strong acids/alkalis, strong oxidizing/reducing agents
Medchemexpress LLC (R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl | 76189-55-4 | MFCD00010805 | 98.0% | 622.67 g·mol⁻¹ | C44H32P2 | 10 G
(R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl is a chiral bisphosphine ligand supplied as a solid research reagent for use in asymmetric synthesis and transition-metal catalysis. It is provided for laboratory research use only and typically appears as a white to pale-yellow crystalline powder suitable for weighing and handling in small-scale reactions.
- Chiral bisphosphine ligand for asymmetric catalysis.
- High reported purity suitable for research applications.
- Solid, crystalline powder, easy to weigh and handle.
- Compatible with common transition-metal catalysts such as palladium and rhodium.
- Used to induce enantioselectivity in organic synthesis.
- Available in small pack sizes for laboratory use.