Tetrakis(triphenylphosphine)palladium, Pd : 9.2 wt.%

Typical Properties
CAS	14221-01-3
Catalog	ACM14221013
Molecular Weight	1155.56 g/mol
Canonical SMILES	[Pd].c1ccc(cc1)P(c2ccccc2)c3ccccc3.c4ccc(cc4)P(c5ccccc5)c6ccccc6.c7ccc(cc7)P(c8ccccc8)c9ccccc9.c%10ccc(cc%10)P(c%11ccccc%11)c%12ccccc%12
InChI	1S/4C18H15P.Pd/c4*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;/h4*1-15H;
InChI Key	NFHFRUOZVGFOOS-UHFFFAOYSA-N
Melting Point	103-107 °C
Purity	99 %
Solubility	Soluble in benzene, toluene, insoluble in ether and alcohol
Appearance	Solid
Storage	2-8 °C
Color	Bright yellow to khaki
Composition	Pd[(C6H5)3P]4
EC Number	238-086-9
MDL Number	MFCD00010012
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

·For elimination reaction, reduction reaction and alkylation reaction;
·Make alkenyl chloride and alkyl lithium or Grignard reagent generate alkene and maintain configuration;
·Make alkenyl chloride and potassium cyanide generate alkenyl cyanide;
·Synthesis of ketones from acid chlorides; deodorization of brominated ketones with hydrogen;
·Preparation of alkynes and enones;
·Cyclization of rings in asymmetric biphenyls;
·Isomerization of diene epoxides, allyl acetate;
·Stereosynthesis of alkenes and 1,4-dienes;
·Dimerization of butadiene.