1415380-62-9 Usage
Description
(S)-1-(2,3-DIFLUOROPHENYL)ETHANAMINE, also known as 2,3-Difluoro-N-(1-phenylethyl)benzenemethanamine, is a chemical compound with the molecular formula C8H10F2N. It is an amine derivative characterized by its 2,3-difluorophenyl and ethanolamine functional groups. (S)-1-(2,3-DIFLUOROPHENYL)ETHANAMINE is commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical products, including potential drugs for the treatment of different medical conditions. Its unique properties and structure make it a versatile and valuable component in the development of new medications, with potential applications in neuroscience, oncology, and infectious diseases.
Uses
Used in Pharmaceutical Industry:
(S)-1-(2,3-DIFLUOROPHENYL)ETHANAMINE is used as a building block for the synthesis of pharmaceutical products for the treatment of various medical conditions. Its unique structure and properties make it a valuable component in the development of new medications.
Used in Neuroscience Applications:
In the field of neuroscience, (S)-1-(2,3-DIFLUOROPHENYL)ETHANAMINE is used as a key component in the development of drugs targeting neurological disorders. Its structure allows for the creation of compounds that can interact with specific receptors or pathways in the nervous system, potentially leading to novel treatments for conditions such as Alzheimer's, Parkinson's, or epilepsy.
Used in Oncology Applications:
In oncology, (S)-1-(2,3-DIFLUOROPHENYL)ETHANAMINE is used as a building block for the synthesis of anticancer drugs. Its unique properties enable the development of compounds that can target cancer cells specifically, potentially leading to more effective and less toxic treatments for various types of cancer.
Used in Infectious Disease Applications:
(S)-1-(2,3-DIFLUOROPHENYL)ETHANAMINE is also used in the development of drugs for the treatment of infectious diseases. Its structure allows for the creation of compounds that can target specific pathogens or disrupt their mechanisms, potentially leading to new treatments for bacterial, viral, or parasitic infections.
Check Digit Verification of cas no
The CAS Registry Mumber 1415380-62-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,3,8 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1415380-62:
(9*1)+(8*4)+(7*1)+(6*5)+(5*3)+(4*8)+(3*0)+(2*6)+(1*2)=139
139 % 10 = 9
So 1415380-62-9 is a valid CAS Registry Number.
1415380-62-9Relevant articles and documents
PROCESS FOR THE PREPARATION OF CHIRAL AMINES FROM PROCHIRAL KETONES
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Page/Page column 5; 6, (2015/12/11)
There is provided a method for the preparation of an enantiomerically enriched amine from a prochiral ketone.
