17245-60-2 Usage
Uses
Used in Pharmaceutical Industry:
3-methyl-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid is used as a key intermediate in the synthesis of pharmaceuticals for its role in creating the molecular structures of various drugs. Its presence in drug molecules can contribute to their therapeutic effects and pharmacological properties.
Used in Drug Development:
In the realm of drug development, 3-methyl-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid is employed as a building block to construct new drug candidates. Its incorporation into drug molecules can enhance their efficacy, selectivity, and potential for treating a range of diseases and conditions.
Used in Medicinal Chemistry Research:
3-methyl-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid is utilized in medicinal chemistry research to explore its potential interactions with biological targets. This can lead to the discovery of new mechanisms of action and the development of innovative therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 17245-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,4 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17245-60:
(7*1)+(6*7)+(5*2)+(4*4)+(3*5)+(2*6)+(1*0)=102
102 % 10 = 2
So 17245-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O3/c1-7-3(4(8)9)2-6-5(7)10/h2H,1H3,(H,6,10)(H,8,9)
17245-60-2Relevant academic research and scientific papers
AMINE-LINKED C3-GLUTARIMIDE DEGRONIMERS FOR TARGET PROTEIN DEGRADATION
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Page/Page column 359-360, (2017/12/01)
This invention provides amine-linked C3-glutarimide Degronimers and Degrons for therapeutic applications as described further herein, and methods of use and compositions thereof as well as methods for their preparation.
Bioinspired total synthesis of agelastatin A
Reyes, Jeremy Chris P.,Romo, Daniel
supporting information; experimental part, p. 6870 - 6873 (2012/10/08)
A one-two punch: Two potentially biosynthetically relevant cyclizations of a keramadine analogue give agelastatin A (see scheme). A diastereoselective C-ring formation, which proceeds through a 5-exo-trig cyclization or a Nazarov cyclization of a red-colored N-acyliminium intermediate, generates the three contiguous stereocenters of the cyclopentane core. A silica gel assisted cyclization of a nagelamide J analogue gives agelastatin A. Copyright
