40438-64-0 Usage
Uses
Used in Chemical Synthesis:
Dicyclohexyl(4-(N,N-dimethylamino)phenyl)phosphine is used as a catalyst in cycloaddition reactions, particularly in the presence of rhodium-catalysts. Its ability to facilitate these reactions makes it a valuable component in the synthesis of complex organic molecules and pharmaceutical compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Dicyclohexyl(4-(N,N-dimethylamino)phenyl)phosphine is utilized as a catalyst for cycloaddition reactions, which are crucial for the synthesis of various drug molecules. Its use in these reactions can lead to the development of new and more effective medications.
Used in Research and Development:
Dicyclohexyl(4-(N,N-dimethylamino)phenyl)phosphine is also employed in research and development settings, where its catalytic properties are studied and optimized for specific chemical reactions. This can contribute to advancements in chemical synthesis techniques and the discovery of new chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 40438-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,3 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40438-64:
(7*4)+(6*0)+(5*4)+(4*3)+(3*8)+(2*6)+(1*4)=100
100 % 10 = 0
So 40438-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H32NP/c1-21(2)17-13-15-20(16-14-17)22(18-9-5-3-6-10-18)19-11-7-4-8-12-19/h13-16,18-19H,3-12H2,1-2H3
40438-64-0Relevant academic research and scientific papers
Method for synthesizing [4-(N,N-dimethylamino)phenyl]dialkylphosphine
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Paragraph 0010; 0011, (2017/10/31)
The invention discloses a method for synthesizing [4-(N,N-dimethylamino)phenyl]dialkylphosphine and belongs to the field of organic synthesis. According to the method, N,N-dimethylaniline as a raw material and 4-dimethylamino-pyridine as a base are reacted, in water-free oxygen-free atmosphere, with dialkyl phosphorous chloride under the catalytic action of cuprous acetate to generate [4-(N,N-dimethylamino)phenyl]dialkylphosphine. Compared with the prior art, the method has the advantages that reaction conditions are mild, operating is simple, the yield is high, the materials are simple and easy to obtain, production cost is reduced and the method is suitable for industrial production.
