224431-84-9 Usage
Uses
Used in Pharmaceutical Industry:
4-Hydroxy-1-piperidineethanol 96 is used as a building block for the synthesis of various pharmaceuticals and organic compounds. Its role in creating enantiomerically pure molecules makes it a crucial component in the development of high-quality drugs and medicinal products.
Used in Asymmetric Synthesis:
4-Hydroxy-1-piperidineethanol 96 is used as a chiral auxiliary in asymmetric synthesis. This application is vital for producing molecules with specific stereochemistry, which is essential for the effectiveness, safety, and selectivity of pharmaceutical compounds.
Used in Chemical Industry:
4-Hydroxy-1-piperidineethanol 96 is utilized in the development of new synthetic methodologies. Its versatility as an intermediate allows for the creation of innovative chemical processes and the synthesis of a wide range of organic compounds.
Used in Research and Development:
4-Hydroxy-1-piperidineethanol 96 is employed in research and development for its potential applications in various fields. Its unique properties and reactivity make it an interesting subject for scientific exploration and the advancement of chemical knowledge.
Check Digit Verification of cas no
The CAS Registry Mumber 224431-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,4,4,3 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 224431-84:
(8*2)+(7*2)+(6*4)+(5*4)+(4*3)+(3*1)+(2*8)+(1*4)=109
109 % 10 = 9
So 224431-84-9 is a valid CAS Registry Number.
224431-84-9Relevant articles and documents
CHEMOKINE RECEPTOR ANTAGONISTS
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Page/Page column 27; 37, (2010/02/13)
A compound of formula (I) or a pharmaceutically acceptable salt or prodrug ester thereof, wherein the variants R, R9, Z, X, Q and Y are defined in the specification.
Estrogen receptor ligands. Part 8: Dihydrobenzoxathiin SERAMs with heteroatom-substituted side chains
Blizzard, Timothy A.,DiNinno, Frank,Morgan II, Jerry D.,Wu, Jane Y.,Chen, Helen Y.,Kim, Seongkon,Chan, Wanda,Birzin, Elizabeth T.,Yang, Yi Tien,Pai, Lee-Yuh,Zhang, Zhoupeng,Hayes, Edward C.,DaSilva, Carolyn A.,Tang, Wei,Rohrer, Susan P.,Schaeffer, James M.,Hammond, Milton L.
, p. 3865 - 3868 (2007/10/03)
A series of benzoxathiin SERAMs with heteroatom-substituted amine side chains was prepared. Minor modifications in the side chain resulted in significant effects on biological activity, especially in uterine tissue.
