443955-98-4 Usage
General Description
The chemical trans-4-Amino-1-Boc-3-hydroxypiperidine is a compound with the molecular formula C11H22N2O3. It is a derivative of 4-Aminopiperidine and is commonly used as a building block in organic synthesis. The Boc (tert-butoxycarbonyl) protecting group attached to the amino group is often used to block the reactivity of the amino group in chemical reactions. The compound plays a crucial role in the synthesis of various pharmaceuticals and organic compounds due to its versatile reactivity and functional group tolerance. It is also used in the development of new chemical entities and drug discovery processes in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 443955-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,9,5 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 443955-98:
(8*4)+(7*4)+(6*3)+(5*9)+(4*5)+(3*5)+(2*9)+(1*8)=184
184 % 10 = 4
So 443955-98-4 is a valid CAS Registry Number.
443955-98-4Relevant 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.
