102165-34-4

Basic information

• Product Name: (dicyclohexylphosphanyl)(phenyl)methanone
• Synonyms: (dicyclohexylphosphanyl)(phenyl)methanone
• CAS NO: 102165-34-4
• Molecular Weight: 302.397
• Mol File: 102165-34-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (dicyclohexylphosphanyl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (dicyclohexylphosphanyl)(phenyl)methanone(102165-34-4)
• EPA Substance Registry System: (dicyclohexylphosphanyl)(phenyl)methanone(102165-34-4)

Safety Data

• Hazardous Substances Data: 102165-34-4(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 829-84-5 dicyclohexylphosphane 

Downstream Products

• 6476-37-5 dicyclohexylphenylphosphine 
• 247940-06-3 CyJohnPhos 

Relevant articles and documents

Palladium-catalyzed C–P(III) bond formation reaction with acylphosphines as phosphorus source

Palladium-catalyzed C–P(III) bond formation reaction employing acylphosphines as the phosphorus source was developed. Under the optimized conditions, acylphosphines could react with aryl halides directly affording trivalent phosphines in up to 94% yield.

ORGANIC MAGNESIUM PHOSPHIDE AND MANUFACTURING METHOD THEREOF, ORGANIC MAGNESIUM PHOSPHIDE COMPLEX AND MANUFACTURING METHOD THEREOF, AND MANUFACTURING METHOD OF ORGANIC PHOSPHORUS COMPOUND USING SAID PHOSPHIDE

An organic magnesium phosphide expressed by Formula (1) below and an organic magnesium phosphide complex expressed by Formula (9) below are provided, and a manufacturing method of organic phosphorus compound is characterized in that the above compounds used as a reagent is reacted with an electrophile: wherein R1 and R2 are each independently an aliphatic group, heteroaliphatic group, alicyclic group, or heterocyclic group, and X is chlorine, bromine, or iodine, wherein R3 and R4 are each independently an aliphatic group, heteroaliphatic group, aromatic group, alicyclic group, or heterocyclic group, and X and Y are each independently chlorine, bromine, or iodine.