914082-74-9 Usage
Uses
Used in Pharmaceutical Industry:
(2S)-2-amino-2-[3-(trifluoromethyl)bicyclo[1.1.1]pent-1-yl]ethanoic acid is used as a building block for the development of novel pharmaceutical compounds due to its unique structure and functional groups. The trifluoromethyl group may impart specific properties that can enhance the activity or selectivity of the resulting drug molecules.
Used in Chemical Research:
In the field of chemical research, (2S)-2-amino-2-[3-(trifluoromethyl)bicyclo[1.1.1]pent-1-yl]ethanoic acid serves as a valuable intermediate or reactant in the synthesis of complex organic molecules. Its unique structure and reactivity can be exploited to explore new chemical reactions and pathways, contributing to the advancement of synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 914082-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,0,8 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 914082-74:
(8*9)+(7*1)+(6*4)+(5*0)+(4*8)+(3*2)+(2*7)+(1*4)=159
159 % 10 = 9
So 914082-74-9 is a valid CAS Registry Number.
914082-74-9Relevant academic research and scientific papers
An optimized protocol for the multigram synthesis of 3-(trifluoromethyl)bicyclo[1.1.1]pent-1-ylglycine (CF3-Bpg)
Mykhailiuk, Pavel K.,Voievoda, Nataliia M.,Afonin, Sergii,Ulrich, Anne S.,Komarov, Igor V.
experimental part, p. 217 - 220 (2010/04/30)
An optimized procedure for the multigram synthesis of 3-(trifluoromethyl)bicyclo[1.1.1]pent-1-ylglycine (CF3-Bpg) has been developed. The overall yield of the synthesis for the optimized up-scaling was increased from 35% to 53%. Moreover, conditions for separating the key isomeric aminonitriles 7 and 8 by crystallization were found, which greatly facilitated the isolation of 8 on a multigram scale. Following this optimized protocol, 100 g of optically pure CF3-Bpg have been synthesized. Crown Copyright
