281652-10-6 Usage
General Description
"Tert-butyl 4,4-difluoropiperidine-1-carboxylate" is a chemical compound with a molecular formula C11H18F2N2O2. It is a fluorinated piperidine derivative that is commonly used in the pharmaceutical and agrochemical industries. tert-butyl 4,4-difluoropiperidine-1-carboxylate is known for its potential medicinal properties and is being studied for its use as a building block in the synthesis of various biologically active compounds. Tert-butyl 4,4-difluoropiperidine-1-carboxylate may also have applications in the development of new drugs and agrochemicals, making it an important compound in the field of medicinal and agricultural chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 281652-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,1,6,5 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 281652-10:
(8*2)+(7*8)+(6*1)+(5*6)+(4*5)+(3*2)+(2*1)+(1*0)=136
136 % 10 = 6
So 281652-10-6 is a valid CAS Registry Number.
281652-10-6Relevant articles and documents
TRPML MODULATORS
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Paragraph 0801, (2021/06/26)
The present invention provides compounds, pharmaceutically acceptable compositions thereof, and methods of using the same.
C-3 NOVEL TRITERPENONE WITH C-28 AMIDE DERIVATIVES AS HIV INHIBITORS
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Paragraph 0178; 0179, (2018/09/12)
The invention relates to C-3 novel triterpenone with C-28 amide derivatives, related compounds, and pharmaceutical compositions useful for the therapeutic treatment of viral diseases and particularly HIV mediated diseases (formula 1).
Eliminative Deoxofluorination Using XtalFluor-E: A One-Step Synthesis of Monofluoroalkenes from Cyclohexanone Derivatives
Vandamme, Mathilde,Paquin, Jean-Fran?ois
supporting information, p. 3604 - 3607 (2017/07/15)
The eliminative deoxofluorination of cyclohexanone derivatives using XtalFluor-E is described. The corresponding monofluoroalkenes are obtained in up to 79% yield. Notably, this one-step procedure occurs at room temperature using readily accessible and cost-effective reagents.