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Home > Products> 55102-19-7
55102-19-7

CHLOROHYDRIDOTRIS(TRIPHENYLPHOSPHINE)RUTHENIUM (II)

Catalog#: AR00DEQC  |   CAS#: 55102-19-7  |   MDL#: MFCD28099802  |   MF: C54H48ClP3Ru  |   MW: 927.4111

Packsize Purity Price Availability Quantity
100mg 98% $39.00 Global Stock Buy Now Add To Cart
250mg 98% $74.00 Global Stock Buy Now Add To Cart
1g 98% $217.00 Global Stock Buy Now Add To Cart
5g 98% $759.00 Global Stock Buy Now Add To Cart
25g 98% $2,659.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DEQC
Chemical Name CHLOROHYDRIDOTRIS(TRIPHENYLPHOSPHINE)RUTHENIUM (II)
CAS Number 55102-19-7
Molecular Formula C54H48ClP3Ru
Molecular Weight 927.4111
MDL Number MFCD28099802
SMILES c1ccc(cc1)P([Ru+2](P(c1ccccc1)(c1ccccc1)c1ccccc1)P(c1ccccc1)(c1ccccc1)c1ccccc1)(c1ccccc1)c1ccccc1.[H-].[Cl-]

$Name$ is a versatile and valuable reagent in chemical synthesis due to its unique properties and reactivity. As a complex containing ruthenium, phosphorus, hydrogen, and chlorine, $Name$ plays a crucial role in catalyzing various important transformations in organic chemistry. One of its key applications is in the hydrogenation of unsaturated bonds, such as alkenes and alkynes, to produce saturated hydrocarbons. This process is vital in the production of a wide range of fine chemicals, pharmaceuticals, and materials.Additionally, $Name$ is widely used in the reduction of functional groups, such as ketones, aldehydes, and imines, to their corresponding alcohols or amines. This reduction process is an essential step in the synthesis of many complex organic molecules. Furthermore, $Name$ has shown excellent performance in mediating various types of carbon-carbon bond-forming reactions, including the reductive coupling of carbonyl compounds and the reductive amination of aldehydes and ketones.Overall, the application of Hydridochlorotris(triphenylphosphine)ruthenium in chemical synthesis highlights its significance as a powerful and efficient catalyst for a wide range of organic transformations, enabling chemists to access novel compounds and streamline synthetic routes.
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