73738-03-1 Usage
Uses
Used in Pharmaceutical Industry:
Diethyl Ethyl-d5-phenylMalonate is used as a key intermediate in the synthesis of Barbital (B118500) and other barbiturate compounds for their pharmacological properties. These barbiturate compounds are known for their sedative, hypnotic, and anticonvulsant effects, making them useful in the treatment of various medical conditions such as insomnia, anxiety, and seizures.
Used in Chemical Research:
As a labeled analogue, Diethyl Ethyl-d5-phenylMalonate is employed in chemical research to study the synthesis, reactions, and properties of barbiturate compounds. The presence of deuterium atoms allows researchers to investigate the behavior of these compounds under different conditions, providing valuable insights into their structure, stability, and reactivity.
Used in Drug Development:
Diethyl Ethyl-d5-phenylMalonate serves as a valuable tool in drug development, particularly in the design and optimization of new barbiturate-based pharmaceuticals. By understanding the synthesis and properties of Diethyl Ethyl-d5-phenylMalonate, researchers can develop more effective and safer medications for various therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 73738-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,3 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73738-03:
(7*7)+(6*3)+(5*7)+(4*3)+(3*8)+(2*0)+(1*3)=141
141 % 10 = 1
So 73738-03-1 is a valid CAS Registry Number.
73738-03-1Relevant academic research and scientific papers
Synthesis and preparation method for phenobarbite-D5 applied to qualitative and quantitative analysis in forensic science
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Paragraph 0034-0035, (2019/11/29)
The invention discloses a synthesis and preparation method for phenobarbite-D5 applied to qualitative and quantitative analysis in forensic science. The synthesis and preparation method comprises thefollowing steps: (1) with 2-phenylmalonate as a raw mate
