26594-41-2 Usage
Description
(5R)-6-(dimethylamino)-5-methyl-4,4-diphenylhexan-3-one is a chiral ketone belonging to the class of organic compounds. As a chiral compound, it possesses a non-superimposable mirror image, which is significant in the field of stereochemistry. Known for its pharmacological properties, this compound has been explored for its potential as a pharmaceutical drug. It is widely utilized in chemical research and development, serving as a reference standard for analytical instrumentation and as a building block for synthesizing other compounds. Its unique structure also contributes to the study of molecular interactions.
Uses
Used in Pharmaceutical Research and Development:
(5R)-6-(dimethylamino)-5-methyl-4,4-diphenylhexan-3-one is used as a pharmaceutical candidate for its potential therapeutic applications. Its pharmacological properties make it a valuable compound for the development of new drugs.
Used in Chemical Research and Development:
In the chemical research and development industry, (5R)-6-(dimethylamino)-5-methyl-4,4-diphenylhexan-3-one is used as a reference standard for analytical instrumentation. Its unique structure and properties allow for accurate measurements and analysis in various chemical processes.
Used in the Synthesis of Other Compounds:
(5R)-6-(dimethylamino)-5-methyl-4,4-diphenylhexan-3-one is used as a building block in the synthesis of other compounds. Its versatile structure enables the creation of new molecules with potential applications in various fields.
Used in the Study of Stereochemistry:
(5R)-6-(dimethylamino)-5-methyl-4,4-diphenylhexan-3-one is used in the study of stereochemistry due to its chiral nature. Understanding the behavior and properties of chiral compounds is crucial for advancing knowledge in chemistry and related fields.
Used in the Study of Molecular Interactions:
(5R)-6-(dimethylamino)-5-methyl-4,4-diphenylhexan-3-one is also used in the study of molecular interactions, as its unique structure provides insights into how molecules interact with each other. This knowledge is essential for developing new materials and understanding biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 26594-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,9 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26594-41:
(7*2)+(6*6)+(5*5)+(4*9)+(3*4)+(2*4)+(1*1)=132
132 % 10 = 2
So 26594-41-2 is a valid CAS Registry Number.