1303973-02-5 Usage
Description
Tert-butyl 3-(aminomethyl)-4-fluoropiperidine-1-carboxylate is a chemical compound with the molecular formula C14H24FN3O2. It is a derivative of piperidine, featuring a fluorine atom and an amino group attached to the piperidine ring. The tert-butyl group and carboxylate moiety are connected to the nitrogen atom of the piperidine ring. tert-butyl 3-(aMinoMethyl)-4-fluoropiperidine-1-carboxylate is widely utilized in organic synthesis and medicinal chemistry as a building block for the preparation of various pharmaceuticals and biologically active molecules. Its distinctive structure and functional groups render it a valuable intermediate in the synthesis of potential drug candidates and research compounds.
Uses
Used in Pharmaceutical Industry:
Tert-butyl 3-(aminomethyl)-4-fluoropiperidine-1-carboxylate is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structures of potential drug candidates. Its presence in these molecules can contribute to the desired pharmacological properties, such as improved binding affinity, selectivity, and bioavailability.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, tert-butyl 3-(aminomethyl)-4-fluoropiperidine-1-carboxylate serves as a versatile building block for the development of biologically active molecules. Researchers use this compound to explore new chemical space and design novel therapeutic agents with specific target interactions and mechanisms of action.
Used in Organic Synthesis:
Tert-butyl 3-(aminomethyl)-4-fluoropiperidine-1-carboxylate is employed as a synthetic precursor in organic synthesis, allowing chemists to construct complex molecular architectures. Its functional groups facilitate various chemical reactions, such as amide bond formation, nucleophilic substitution, and reductive amination, which are crucial for the assembly of diverse organic compounds.
Overall, the unique structural features and functional groups of tert-butyl 3-(aminomethyl)-4-fluoropiperidine-1-carboxylate make it a valuable asset in the fields of pharmaceuticals, medicinal chemistry, and organic synthesis, where it plays a pivotal role in the development of innovative therapeutic agents and the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 1303973-02-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,3,9,7 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1303973-02:
(9*1)+(8*3)+(7*0)+(6*3)+(5*9)+(4*7)+(3*3)+(2*0)+(1*2)=135
135 % 10 = 5
So 1303973-02-5 is a valid CAS Registry Number.
