1064076-86-3 Usage
Uses
Used in Pharmaceutical Research:
(2S)-4-fluoro-4-methyl-2-((1S)-2,2,2-trifluoro-1-[4'-(methylsulfonyl)biphenyl-4-yl]ethylamino)pentanoic acid dicyclohexylamine salt is used as a research compound for exploring its potential therapeutic properties and applications in the pharmaceutical industry.
Used in Drug Development:
In the drug development industry, (2S)-4-fluoro-4-methyl-2-((1S)-2,2,2-trifluoro-1-[4'-(methylsulfonyl)biphenyl-4-yl]ethylamino)pentanoic acid dicyclohexylamine salt is utilized as a candidate molecule for the development of new medications, given its potential biomedical applications.
Note: The specific applications and industries for (2S)-4-fluoro-4-methyl-2-({(1S)-2,2,2-trifluoro-1-[4'-(methylsulfonyl)biphenyl-4-yl]ethyl}amino)pentanoic acid dicyclohexylamine salt are not provided in the materials. The uses listed above are general and based on the potential pharmaceutical applications mentioned. Further research and development would be required to determine the exact uses and industries where (2S)-4-fluoro-4-methyl-2-({(1S)-2,2,2-trifluoro-1-[4'-(methylsulfonyl)biphenyl-4-yl]ethyl}amino)pentanoic acid dicyclohexylamine salt could be applied.
Check Digit Verification of cas no
The CAS Registry Mumber 1064076-86-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,4,0,7 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1064076-86:
(9*1)+(8*0)+(7*6)+(6*4)+(5*0)+(4*7)+(3*6)+(2*8)+(1*6)=143
143 % 10 = 3
So 1064076-86-3 is a valid CAS Registry Number.
1064076-86-3Relevant academic research and scientific papers
AMIDATION PROCESS
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, (2012/11/13)
This invention describes an amidation process whereby perfluorinated amino acids can be activated and treated with an amine in the presence of a coupling agent and a pyridine derivative to yield amides, without loss of optical purity.
AMIDATION PROCESS FOR THE PREPARATION OF CATHEPSIN K INHIBITORS
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Page/Page column 7-8, (2008/12/04)
This invention describes an amidation process whereby amino acids of the Formulae IIA or IIB can be activated and treated with an amine in the presence of a base to yield amides of the Formula (I), without loss of optical purity.
Diastereoselective reductive amination process
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Page/Page column 10, (2010/02/15)
This invention describes a reductive amination process whereby perfluorinated ketones or ketals are combined with α-aminoesters under basic conditions to form metal carboxylates. Diastereoselective reductions of the metal carboxylates enable access to two
