1331777-74-2 Usage
General Description
Cis-4-Amino-1-Boc-3-hydroxypiperidine is a chemical compound with the molecular formula C11H21N3O3. It is a derivative of piperidine and contains an amino group and a Boc (tert-butoxycarbonyl) protecting group. cis-4-AMino-1-Boc-3-hydro... is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals and bioactive molecules. It can also be utilized in the production of peptide and peptide-like structures. The Boc protecting group allows for selective deprotection and further functionalization of the molecule, making it a valuable tool in synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1331777-74-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,1,7,7 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1331777-74:
(9*1)+(8*3)+(7*3)+(6*1)+(5*7)+(4*7)+(3*7)+(2*7)+(1*4)=162
162 % 10 = 2
So 1331777-74-2 is a valid CAS Registry Number.
1331777-74-2Relevant articles and documents
TBK/IKK INHIBITOR COMPOUNDS AND USES THEREOF
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, (2017/01/23)
The present invention relates to compounds of Formula I and pharmaceutically acceptable compositions thereof, useful as TBK/IKKε inhibitors.
PYRROLO[2,3-D]PYRIMIDINYL, PYRROLO[2,3-B]PYRAZINYL AND PYR-ROLO[2,3-D]PYRIDINYL ACRYLAMIDES
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Paragraph 0473, (2015/06/17)
The present invention provides pharmaceutically active pyrrolo[2,3-d]pyrimidinyl and pyrrolo[2,3-d]pyridinyl acrylamides and analogues thereof. Such compounds are useful for inhibiting Janus Kinase (JAK). This invention also is directed to compositions comprising methods for making such compounds, and methods for treating and preventing conditions mediated by JAK.
METHYLPYRROLOPYRIMIDINECARBOXAMIDES
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Page/Page column 109, (2012/06/18)
The compounds of Formula (I), wherein R1, R2, R21, R22, R23, R24, Y and R3 have the meanings as given in the description, the salts thereof, the stereoisomers of the compounds and the salts thereof are effective inhibitors of the type 5 phosphodiesterase.