849107-00-2 Usage
Uses
Used in Pharmaceutical Research:
(S)-tert-butyl 3-(isopropylamino)pyrrolidine-1-carboxylate is used as a building block in the synthesis of peptides and proteins for pharmaceutical research. Its steric hindrance and structural stability make it an important component in the development of bioactive molecules with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-tert-butyl 3-(isopropylamino)pyrrolidine-1-carboxylate is used as a key intermediate for the preparation of various complex organic compounds. Its unique structural features facilitate the synthesis of target molecules with specific properties and functions.
Used in Medicinal Chemistry:
(S)-tert-butyl 3-(isopropylamino)pyrrolidine-1-carboxylate is employed as a structural element in the design of novel bioactive molecules for medicinal chemistry. Its ability to control stereochemistry and provide stability makes it a valuable tool in the development of new drugs with improved efficacy and selectivity.
Used in Drug Discovery:
In drug discovery, (S)-tert-butyl 3-(isopropylamino)pyrrolidine-1-carboxylate is utilized as a starting material for the development of new pharmaceutical agents. Its versatility and structural features enable the exploration of diverse chemical space and the identification of potential drug candidates with novel mechanisms of action.
Used in Stereochemistry Control:
(S)-tert-butyl 3-(isopropylamino)pyrrolidine-1-carboxylate is used as a chiral auxiliary in controlling the stereochemistry of chemical reactions. Its presence helps to dictate the spatial arrangement of atoms in the synthesis of enantiomerically pure compounds, which is crucial for the development of chiral drugs with desired biological activities.
Used in Bioactive Molecule Design:
In the design of bioactive molecules, (S)-tert-butyl 3-(isopropylamino)pyrrolidine-1-carboxylate is used as a structural motif to impart stability and rigidity. Its incorporation into molecular frameworks can enhance the binding affinity and selectivity of drug candidates, leading to improved therapeutic outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 849107-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,1,0 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 849107-00:
(8*8)+(7*4)+(6*9)+(5*1)+(4*0)+(3*7)+(2*0)+(1*0)=172
172 % 10 = 2
So 849107-00-2 is a valid CAS Registry Number.
849107-00-2Relevant academic research and scientific papers
HETEROCYCLIC COMPOUNDS
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Paragraph 00241, (2015/10/05)
Provided herein are compounds of formula I and compositions containing the compounds. The compounds and compositions are useful in the methods of inhibiting the action of ERK5, a BET family protein or both. In certain embodiments, the compounds and compositions are useful in the prevention, amelioration or treatment of a ERK5-mediated disease, a BET protein-mediated disease or both
AMINOPYRIMIDINES USEFUL AS KINASE INHIBITORS
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Page/Page column 31, (2010/06/16)
The present invention relates to compounds useful as inhibitors of Aurora protein kinases. The invention also provides pharmaceutically acceptable compositions comprising those compounds and methods of using the compounds and compositions in the treatment
