86941-24-4 Usage
Description
1-(4-2-[2-(4-fluorophenyl)ethoxy]ethoxyphenoxy)-3-(propan-2-ylamino)propan-2-ol is a complex organic compound characterized by its multiple functional groups, including a primary alcohol group, an amino group, and an ether linkage. 1-(4-2-[2-(4-fluorophenyl)ethoxy]ethoxyphenoxy)-3-(propan-2-ylamino)propan-2-ol features a central propanol backbone with a substituted phenyl ring connected to two ethylene glycol chains and a propan-2-ylamine group. Its structural complexity renders it a promising candidate for various pharmacological and medicinal applications, particularly in the treatment of cardiovascular or neurological disorders.
Uses
Used in Pharmaceutical Industry:
1-(4-2-[2-(4-fluorophenyl)ethoxy]ethoxyphenoxy)-3-(propan-2-ylamino)propan-2-ol is used as a potential therapeutic agent for the treatment of cardiovascular or neurological disorders due to its complex structure and multiple functional groups, which may interact with various biological targets.
Used in Drug Development:
In the field of drug development, 1-(4-2-[2-(4-fluorophenyl)ethoxy]ethoxyphenoxy)-3-(propan-2-ylamino)propan-2-ol can be utilized as a lead compound for the design and synthesis of new drugs targeting specific receptors or enzymes involved in cardiovascular and neurological conditions. Its structural features may be optimized to enhance potency, selectivity, and pharmacokinetic properties.
Used in Medicinal Chemistry Research:
1-(4-2-[2-(4-fluorophenyl)ethoxy]ethoxyphenoxy)-3-(propan-2-ylamino)propan-2-ol serves as a valuable compound in medicinal chemistry research for understanding the structure-activity relationships of various biologically active molecules. Its unique structural elements can provide insights into the design of more effective and safer drugs for treating different diseases.
Used in Chemical Synthesis:
1-(4-2-[2-(4-fluorophenyl)ethoxy]ethoxyphenoxy)-3-(propan-2-ylamino)propan-2-ol can also be employed as a synthetic building block or intermediate in the preparation of other complex organic molecules, particularly those with potential applications in the pharmaceutical and chemical industries. Its versatile functional groups allow for further chemical modifications and the creation of novel compounds with tailored properties.
Check Digit Verification of cas no
The CAS Registry Mumber 86941-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,4 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86941-24:
(7*8)+(6*6)+(5*9)+(4*4)+(3*1)+(2*2)+(1*4)=164
164 % 10 = 4
So 86941-24-4 is a valid CAS Registry Number.
86941-24-4Relevant articles and documents
β1-Selective Adrenoceptor Antagonists. 2. 4-Ether-Linked Phenoxypropanolamines
Machin, Peter J.,Hurst, David N.,Bradshaw, Rachel M.,Blaber, Leslie C.,Burden, David T.,et al.
, p. 1570 - 1576 (2007/10/02)
A series of 4-substituted phenoxypropanolamines was prepared and examined for β-adrenoceptor activity.Some of the compounds, especially the oxy>ethoxy>phenoxy>propanolamines (14, 15, and 24), showed potent β1-blo
