307525-88-8 Usage
Ethyl ester derivative
Piperidine-4-carboxylic acid The compound is derived from piperidine-4-carboxylic acid by attaching an ethyl ester group to it.
Phenylcarbamoyl group
Presence of a phenyl ring attached to a carbamoyl group (-NH2) This group contributes to the compound's structure and potential medicinal properties.
Intermediate in pharmaceutical synthesis
The compound is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds, making it a valuable building block in drug development.
Potential medicinal properties
1-PHENYLCARBAMOYL-PIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER has been studied for its potential in treating neurological and psychiatric disorders, highlighting its importance in medicinal chemistry.
Scientific interest
The compound's chemical structure and biological activity make it a subject of ongoing research, as scientists continue to explore its potential applications and effects.
Check Digit Verification of cas no
The CAS Registry Mumber 307525-88-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,7,5,2 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 307525-88:
(8*3)+(7*0)+(6*7)+(5*5)+(4*2)+(3*5)+(2*8)+(1*8)=138
138 % 10 = 8
So 307525-88-8 is a valid CAS Registry Number.
307525-88-8Relevant articles and documents
Method for preparing asymmetric urea compound (by machine translation)
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Paragraph 0043-0048; 0073-0078, (2020/03/25)
The invention provides a vehicle CO. 2 A method. for synthesizing an asymmetric urea compound by carbonylation coupling reaction of the carbonylation reagent is: and the aromatic, aliphatic primary amine compound and the aliphatic secondary amine compound and the normal pressure (100 °C, diglyme), can be efficiently prepared by using a common Lewis base and a hydrogen silane as the accelerator/CO under mild conditions. 2 The reaction produces a corresponding asymmetric urea compound. containing different functional groups, the process being operated at atmospheric pressure CO. 2 The use of an inexpensive Lewis base and, industrial silicon waste PMHS( for the green non-toxic carbonylation reagent) avoids toxic carbonylation reagents, high pressure, as an accelerator CO. 2 , The use, of the expensive dehydrating agent and the noble metal does not need to purify and separate the intermediate, and the pure product, is obtained by simple suction filtration separation after the reaction is ended . is a high efficiency, novel synthetic method . The commercial herbicide NEBURON. is successfully prepared by using the method. (by machine translation)
