triphenylphosphine rhodium chloride

Typical Properties
CAS	14694-95-2
Catalog	ACM14694952
Molecular Weight	925.22 g/mol
Canonical SMILES	Cl[Rh].c1ccc(cc1)P(c2ccccc2)c3ccccc3.c4ccc(cc4)P(c5ccccc5)c6ccccc6.c7ccc(cc7)P(c8ccccc8)c9ccccc9
InChI	1S/3C18H15P.ClH.Rh/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;/h3*1-15H;1H;/q;;;;+1/p-1
InChI Key	IXAYKDDZKIZSPV-UHFFFAOYSA-M
Melting Point	245-250 °C (dec.)
Purity	97 %
Solubility	Soluble in most solvents (e.g. benzene, ethanol, chloroform, dichloromethane) but with phosphine dissociation. Reacts with O{2} in solution
Appearance	Powder
Storage	Room Temp
Color	Red-brown to maroon
Composition	[(C6H5)3P]3RhCl
Concentration	Rh : 11.1 wt.%
EC Number	238-744-5
MDL Number	MFCD00010016
Quality Level	200
Shipping	Ambient

Overview

Description

Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields.

Features

·High catalytic activity
·Good selectivity
·Use safety
·High temperature resistance, oxidation resistance, corrosion resistance
·Recyclable recycling processing

Application

·Efficient hydrogenation catalyst and complexing agent;
·Selective hydrogenation, transfer hydrogenation;
·Hydrogenation and hydroformylation of alkenes and alkynes;
·Cyclization of 4-alkenals;
·Reductive decarbonylation of aldehydes; desulphurization of xanthyl halides;
·Reduction of diazofluoroborate;
·Hydrosilylation of carbonyl groups;
·Splitting of allyl ethers, etc.