55883-24-4 Usage
Uses
Used in Pharmaceutical Research:
1-(4-chlorophenoxy)-3-(piperidin-1-yl)propan-2-ol is used as a research compound for exploring its potential as a beta-adrenergic agonist or antagonist, which could be significant in the development of medications targeting the cardiovascular system.
Used in Organic Synthesis:
As a building block in organic synthesis, 1-(4-chlorophenoxy)-3-(piperidin-1-yl)propan-2-ol is used for creating more complex molecules that may have various applications in the chemical and pharmaceutical industries.
Used in the Treatment of Cardiovascular Disorders:
1-(4-chlorophenoxy)-3-(piperidin-1-yl)propan-2-ol is used as a potential therapeutic agent for cardiovascular conditions, given its possible beta-adrenergic activity.
Used in the Treatment of Neurological Disorders:
1-(4-chlorophenoxy)-3-(piperidin-1-yl)propan-2-ol is also used as a potential therapeutic agent for neurological disorders, possibly due to its central nervous system depressant properties.
Check Digit Verification of cas no
The CAS Registry Mumber 55883-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,8 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55883-24:
(7*5)+(6*5)+(5*8)+(4*8)+(3*3)+(2*2)+(1*4)=154
154 % 10 = 4
So 55883-24-4 is a valid CAS Registry Number.
55883-24-4Relevant articles and documents
Phenalenyl in a different role: Catalytic activation through the nonbonding molecular orbital
Raha Roy, Sudipta,Nijamudheen,Pariyar, Anand,Ghosh, Anup,Vardhanapu, Pavan K.,Mandal, Prasun K.,Datta, Ayan,Mandal, Swadhin K.
, p. 4307 - 4319 (2015/02/19)
We have demonstrated that the nonbonding molecular orbital (NBMO) of the phenalenyl (PLY) cation can be used as a Lewis acid catalyst for different organic transformations. Detailed computational and spectroscopic studies for the aminolysis reaction of ep
Process for the solid state synthesis of enantiopure B-aminoalcohols from racemic epoxides
-
, (2008/06/13)
The invention relates to a process for the solid state synthesis of enantiopure β-aminoalcohols by preparing inclusion complexes of aryloxyepoxide with cyclodextrin by adding an epoxide in equimolar ratio in an organic solvent to an aqueous solution of cyclodextrin, reacting the cyclodextrin complex of aryloxyepoxide with a nucleophile in solid state by intimately grinding the mixture using a mortar and pestle, continuing the mixing till the starting epoxide disappeared on tic, removing excess amines under vacuum, extracting the β-aminoalcohols produced with a solvent with yields of more than 50% and enantioselectivity of upto 100%.
