1997-41-7 Usage
Description
5-(TRIFLUOROMETHYL)ISOINDOLINE-1,3-DIONE is a chemical compound with the molecular formula C9H5F3NO2. It is a fluorinated isoindoline-1,3-dione derivative that has a trifluoromethyl group attached to the carbon atom in the 5-position of the isoindoline ring.
Uses
Used in Pharmaceutical and Agrochemical Industries:
5-(TRIFLUOROMETHYL)ISOINDOLINE-1,3-DIONE is used as a building block in the synthesis of pharmaceuticals and agrochemicals due to its unique structural and chemical properties.
Used in Organic Synthesis and Medicinal Chemistry:
5-(TRIFLUOROMETHYL)ISOINDOLINE-1,3-DIONE is used as a reagent in organic synthesis and medicinal chemistry for the preparation of diverse bioactive molecules.
Used in Material Science:
5-(TRIFLUOROMETHYL)ISOINDOLINE-1,3-DIONE has been studied for its potential applications in material science, such as in the development of novel polymers and molecular devices for electronic and optoelectronic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1997-41-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1997-41:
(6*1)+(5*9)+(4*9)+(3*7)+(2*4)+(1*1)=117
117 % 10 = 7
So 1997-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H4F3NO2/c10-9(11,12)4-1-2-5-6(3-4)8(15)13-7(5)14/h1-3H,(H,13,14,15)
1997-41-7Relevant articles and documents
Inhibitors of dipeptidyl peptidase 8 and dipeptidyl peptidase 9. Part 2: Isoindoline containing inhibitors
Van Goethem, Sebastiaan,Van der Veken, Pieter,Dubois, Veronique,Soroka, Anna,Lambeir, Anne-Marie,Chen, Xin,Haemers, Achiel,Scharpe, Simon,De Meester, Ingrid,Augustyns, Koen
scheme or table, p. 4159 - 4162 (2009/05/07)
To obtain selective and potent inhibitors of dipeptidyl peptidases 8 and 9, we synthesized a series of substituted isoindolines as modified analogs of allo-Ile-isoindoline, the reference DPP8/9 inhibitor. The influence of phenyl substituents and different P2 residues on the inhibitors' affinity toward other DPPs and more specifically, their potential to discriminate between DPP8 and DPP9 will be discussed. Within this series compound 8j was shown to be a potent and selective inhibitor of DPP8/9 with low activity toward DPP II.
A CONVENIENT SYNTHESIS OF TRIFLUOROMETHYL SUBSTITUTED PHTHALOCYANINES
Pawlowski, Georg,Hanack, Michael
, p. 351 - 364 (2007/10/02)
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