63744-11-6 Usage
Uses
Used in Organometallic Chemistry:
BIS(TRIMETHYLSILYL)AMIDODIMETHYLPHOSPHINE is used as a phosphine ligand for the formation of organometallic complexes, which are essential in various chemical reactions and processes. Its ability to bind with transition metals allows for the creation of stable and reactive intermediates that can be used in a variety of applications.
Used in Catalysis:
In the field of catalysis, BIS(TRIMETHYLSILYL)AMIDODIMETHYLPHOSPHINE is used as a ligand to enhance the efficiency and selectivity of catalytic reactions. Its presence can improve the activity of catalysts and facilitate reactions that would otherwise be difficult or impossible to achieve.
Used in Synthetic Chemistry:
BIS(TRIMETHYLSILYL)AMIDODIMETHYLPHOSPHINE is used as a reagent in synthetic chemistry for the synthesis of various organic and inorganic compounds. Its versatility and stability make it a valuable tool for chemists working on the development of new materials and pharmaceuticals.
Used in Chemical Research:
In chemical research, BIS(TRIMETHYLSILYL)AMIDODIMETHYLPHOSPHINE is used as a research tool to study the properties and behavior of organometallic complexes and catalytic systems. Its unique structure and reactivity provide insights into the mechanisms of various chemical reactions and help in the development of new synthetic methods and catalysts.
Used in Pharmaceutical Industry:
BIS(TRIMETHYLSILYL)AMIDODIMETHYLPHOSPHINE is used as a catalyst or intermediate in the synthesis of pharmaceutical compounds. Its ability to facilitate complex reactions and improve the efficiency of catalytic processes can lead to the development of new drugs and drug delivery systems.
Used in Material Science:
In material science, BIS(TRIMETHYLSILYL)AMIDODIMETHYLPHOSPHINE is used in the development of new materials with unique properties. Its role in organometallic chemistry and catalysis can contribute to the synthesis of advanced materials for various applications, such as electronics, energy storage, and nanotechnology.
Check Digit Verification of cas no
The CAS Registry Mumber 63744-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,4 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63744-11:
(7*6)+(6*3)+(5*7)+(4*4)+(3*4)+(2*1)+(1*1)=126
126 % 10 = 6
So 63744-11-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H24NPSi2/c1-10(2)9(11(3,4)5)12(6,7)8/h1-8H3
63744-11-6Relevant articles and documents
Synthesis and some oxidation reactions of [bis(trimethylsilyl)amino]dimethylphosphine
Wilburn, James C.,Neilson, Robert H.
, p. 2519 - 2521 (1977)
The synthesis, characterization, and some reactions of [bis(trimethylsilyl)amino]dimethylphosphine (1) are reported. Although compound 1 was routinely prepared via the reaction of LiN(SiMe3)2 and Me2PCl, it was also isolat
RAW MATERIAL FOR FORMING THIN FILM AND MANUFACTURING METHOD FOR THIN FILM
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Paragraph 0056, (2016/12/12)
PROBLEM TO BE SOLVED: To provide a raw material for forming a thin film excellent in thermal stability, reactivity with reactive gas and step coverage property and capable of being applied to an ALD method, and to provide a raw material for forming a thin film capable of providing the thin film having the content of phosphorus of 10 to 20 mass%. SOLUTION: A raw material for forming a thin film has a silicon compound represented by the general formula (1). In the formula (1), R1 to R3 represent each independently an alkyl group having 1 to 4 carbon atoms and X represents a monovalent organic residue having a phosphorus element. COPYRIGHT: (C)2015,JPOandINPIT
Dimethylsilylaminophosphane heterocyclization of isothiocyanates to diazaphosphole-thiones through zwitterionic intermediates
Petrov, Petar Y.,Angelov, Christo M.,McDonald, Robert,Alexiev, Alexi,Cavell, Ronald G.
scheme or table, p. 196 - 202 (2011/07/09)
Isothiocyanates react with Me2P- N(SiMe3)2 with elimination of (Me3Si)2Stogivenew structurally characterized heterocyclic diazaphosphole derivatives, and in one case the intermediate zwitteri- onic compound was isolated and structurally characterized.
