325152-99-6 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-2-Amino-2-(3-trifluoromethylphenyl)ethanol is used as an intermediate in the pharmaceutical industry for the synthesis of various pharmaceutical compounds. Its unique structure, including the trifluoromethyl group, allows for the creation of molecules with specific biological activities and properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-2-Amino-2-(3-trifluoromethylphenyl)ethanol serves as a valuable building block for designing and developing new drugs. Its chiral nature and functional groups enable the creation of enantiomerically pure compounds with potential therapeutic applications.
Used in Drug Development:
(S)-2-Amino-2-(3-trifluoromethylphenyl)ethanol is also utilized in drug development, where it can be employed to create novel drug candidates with improved pharmacological profiles. (S)-2-AMino-2-(3-trifluoroMethylphenyl)ethanol's interactions with biological targets can be fine-tuned through structural modifications, potentially leading to more effective and safer medications.
Note: Since the provided materials do not specify particular applications in different industries, the uses listed above are general applications based on the compound's properties and potential in the pharmaceutical and medicinal chemistry fields.
Check Digit Verification of cas no
The CAS Registry Mumber 325152-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,5,1,5 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 325152-99:
(8*3)+(7*2)+(6*5)+(5*1)+(4*5)+(3*2)+(2*9)+(1*9)=126
126 % 10 = 6
So 325152-99-6 is a valid CAS Registry Number.
325152-99-6Relevant articles and documents
A general asymmetric synthesis of phenylglycinols
Pan, Xingang,Jia, Liangbin,Liu, Xuejian,Ma, Haikuo,Yang, Wenqian,Schwarz, Jacob B.
, p. 329 - 337 (2011/05/17)
Hydride reduction and deprotection of siloxymethyl sulfinimines 2 reliably furnished chiral phenylglycinols 1 or 10 in high overall yield and enantiomeric purity.
