102151-71-3 Usage
Uses
Used in Veterinary Medicine:
2-(4-methoxyphenyl)-1H-Imidazole-5-carboxamide is used as an anti-inflammatory agent for the treatment of pain and inflammation associated with conditions such as osteoarthritis in dogs and cats. It is particularly effective in relieving pain and inflammation in animal studies and is commonly used for the management of musculoskeletal conditions in pets.
Used in Pain and Inflammation Management:
2-(4-methoxyphenyl)-1H-Imidazole-5-carboxamide is used as a therapeutic agent for managing pain and inflammation in animals, providing relief from discomfort and improving the quality of life for pets suffering from musculoskeletal conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 102151-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,5 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102151-71:
(8*1)+(7*0)+(6*2)+(5*1)+(4*5)+(3*1)+(2*7)+(1*1)=63
63 % 10 = 3
So 102151-71-3 is a valid CAS Registry Number.
102151-71-3Relevant academic research and scientific papers
BETA-BLOCKING SUBSTITUTED IMIDAZOLES
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, (2008/06/13)
Novel substituted imidazoles and methods for their preparation are disclosed. These imidazoles, and their salts, exhibit pharmacological activity which includes antihypertensive activity and β-adrenergic blocking activity.
BETA-ADRENERGIC BLOCKING IMIDAZOLYLPHENOXY PROPANOLAMINES
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, (2008/06/13)
Substituted imidazoles and methods for their preparation are disclosed. These imidazoles, and their salts, exhibit pharmacological activity which includes antihypertensive activity and β-adrenergic blocking activity. STR1
β1-Selective Adrenoceptor Antagonists: Examples of the 2-phenyl>imidazole Class. 2
Baldwin, John J.,Christy, Marcia E.,Denny, George H.,Habecker, Charles N.,Freedman, Mark B.,et al.
, p. 1065 - 1080 (2007/10/02)
An attempt to develop a highly cardioselective β-adrenoceptor antagonist devoid of intrinsic sympathomimetic activity (ISA) focused on exploring structure-activity relationships around (S)--amino>-2-hydroxypropoxy>phen
