1025437-77-7 Usage
Description
[1,1'-Biphenyl]-4-carboxamide, 4'-chloro-N-[(1S)-3-(dimethylamino)-1-(2-naphthalenyl)propyl]is a complex organic chemical compound characterized by its molecular formula C28H27ClN2O. It is a derivative of biphenyl, featuring a carboxamide group, a chloro substituent, a dimethylamino group, and a naphthalenyl moiety. [1,1'-Biphenyl]-4-carboxamide, 4'-chloro-N-[(1S)-3-(dimethylamino)-1-(2-naphthalenyl)propyl]-'s stereochemistry is defined by the (1S) configuration at the chiral center, which may influence its potential applications in various fields, including pharmaceutical research.
Uses
Since the provided materials do not specify the uses of [1,1'-Biphenyl]-4-carboxamide, 4'-chloro-N-[(1S)-3-(dimethylamino)-1-(2-naphthalenyl)propyl]-, we can only hypothesize potential applications based on its structural features and the general utility of similar compounds:
Used in Pharmaceutical Research:
[1,1'-Biphenyl]-4-carboxamide, 4'-chloro-N-[(1S)-3-(dimethylamino)-1-(2-naphthalenyl)propyl]may be used as a research compound for the development of new pharmaceuticals, given its unique structural features and the potential for interaction with biological targets due to its various functional groups.
Used in Chemical Synthesis:
[1,1'-Biphenyl]-4-carboxamide, 4'-chloro-N-[(1S)-3-(dimethylamino)-1-(2-naphthalenyl)propyl]could also be utilized as an intermediate or building block in the synthesis of more complex molecules, particularly in the fields of organic chemistry and materials science.
Used in Analytical Chemistry:
Due to its specific stereochemistry and functional groups, [1,1'-Biphenyl]-4-carboxamide, 4'-chloro-N-[(1S)-3-(dimethylamino)-1-(2-naphthalenyl)propyl]might be employed in analytical chemistry for the development of new methods or techniques for the separation, detection, or analysis of chiral compounds.
Please note that these uses are speculative and would require further research and validation to confirm their applicability.
Check Digit Verification of cas no
The CAS Registry Mumber 1025437-77-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,4,3 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1025437-77:
(9*1)+(8*0)+(7*2)+(6*5)+(5*4)+(4*3)+(3*7)+(2*7)+(1*7)=127
127 % 10 = 7
So 1025437-77-7 is a valid CAS Registry Number.
1025437-77-7Relevant articles and documents
Novel and potent small-molecule urotensin II receptor agonists
Lehmann, Fredrik,Currier, Erika A.,Clemons, Bryan,Hansen, Lars K.,Olsson, Roger,Hacksell, Uli,Luthman, Kristina
experimental part, p. 4657 - 4665 (2009/12/06)
A series of analogs of the non-peptidic urotensin II receptor agonist N-[1-(4-chlorophenyl)-3-(dimethylamino)propyl]-4-phenylbenzamide (FL104) has been synthesized and evaluated pharmacologically. The enantiomers of the two most potent racemic analogues were obtained from the corresponding diastereomeric mandelic amides. In agreement with previously observed SAR, most of the agonist potency resided in the (S) enantiomers. The most potent UII receptor agonist in the new series was (S)-N-[3-dimethylamino-1-(2-naphthyl)propyl]-4-(4-chlorophenyl)benzamide (EC50 = 23 nM at the urotensin II receptor).
