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Phosphorane, [bis(trimethylsilyl)methylene](dicyclohexylphosphino)diphenylis a chemical compound that contains a phosphorane group and is used in organic synthesis. It is known for its ability to stabilize and control reactive intermediates in chemical reactions and is often used as a precursor in the preparation of other organic compounds.

91325-92-7

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91325-92-7 Usage

Uses

Used in Organic Synthesis:
Phosphorane, [bis(trimethylsilyl)methylene](dicyclohexylphosphino)diphenylis used as a precursor in the preparation of other organic compounds due to its ability to stabilize and control reactive intermediates in chemical reactions.
Used in Coordination Chemistry:
Phosphorane, [bis(trimethylsilyl)methylene](dicyclohexylphosphino)diphenylis used as a ligand in coordination chemistry and can form complexes with transition metal ions, thereby facilitating various catalytic processes.
Used in Pharmaceutical Industry:
Phosphorane, [bis(trimethylsilyl)methylene](dicyclohexylphosphino)diphenylhas potential applications in the pharmaceutical industry due to its unique chemical properties.
Used in Advanced Materials Development:
Phosphorane, [bis(trimethylsilyl)methylene](dicyclohexylphosphino)diphenylhas potential applications in the development of advanced materials due to its unique chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 91325-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,2 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91325-92:
(7*9)+(6*1)+(5*3)+(4*2)+(3*5)+(2*9)+(1*2)=127
127 % 10 = 7
So 91325-92-7 is a valid CAS Registry Number.

91325-92-7Downstream Products

91325-92-7Relevant academic research and scientific papers

Ambivalent Reactions of Phosphanes Metallated in α-Position with n-Butyllithium

Appel, Rolf,Haubrich, Gerhard,Knoch, Falk

, p. 2063 - 2075 (2007/10/02)

The reaction of diphenyl(trimethylsilylmethyl)phosphane (1) with n-butyllithium yields the lithium methanide 2, which reacts with chlorotrimethylsilane to form diphenylphosphane (3).Repeated lithiation yields the ambivalent inte

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