1363382-00-6 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 1-Boc-3-fluoroazetidine-3-carboxylate is used as a key intermediate for the synthesis of various pharmaceuticals due to its ability to interact with biological proteins. Its presence of fluorine allows for deep penetration into protein active sites, making it a valuable component in drug development.
Used in Medicinal Chemistry Research:
Methyl 1-Boc-3-fluoroazetidine-3-carboxylate is used as a research compound for exploring its potential in the synthesis of new drugs and understanding its interactions with biological proteins. This can lead to the discovery of novel therapeutic agents and advancements in medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1363382-00-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,3,8 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1363382-00:
(9*1)+(8*3)+(7*6)+(6*3)+(5*3)+(4*8)+(3*2)+(2*0)+(1*0)=146
146 % 10 = 6
So 1363382-00-6 is a valid CAS Registry Number.
1363382-00-6Relevant academic research and scientific papers
TARGETING COMPOUNDS
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Paragraph 0314; 0316, (2019/07/19)
The disclosure provides, at least in part, liver, intestine and/or kidney-targeting compounds and their use in treating liver, intestine and/or kidney disorders, such as non-alcoholic steatohepatitis, alcoholic steatohepatitis, hepatocellular carcinoma, liver cirrhosis, and hepatitis B; and/or chronic kidney disease, glomerular disease such as IGA nephropathy, lupus nephritis, or polycystic kidney disease. The compounds are contemplated to have activity against methionyl aminopeptidase 2.
Synthetic method of 3-fluoro-azetidine derivative
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, (2016/10/07)
The invention provides a synthetic method of a 3-fluoro-azetidine derivative. The synthetic method takes a compound I as the raw material, the compound I is reacted with trimethylsilyl cyanide to obtain a compound II, and a compound VI is obtained through
