877681-12-4 Usage
Description
5-TRIFLUOROMETHOXY-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE is a chemical compound with the molecular formula C8H7F3N2O2. It is a benzimidazole derivative with a trifluoromethoxy group attached to the benzene ring. This unique structure and properties make it a promising candidate for various applications in pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
5-TRIFLUOROMETHOXY-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE is used as a building block in the synthesis of new drugs. Its unique structure allows for the development of innovative therapeutic agents with potential applications in treating various diseases and conditions.
Used in Agrochemical Industry:
5-TRIFLUOROMETHOXY-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE is used as an intermediate in the production of agrochemicals. Its properties can contribute to the development of new pesticides, herbicides, or other agricultural chemicals that can improve crop yield and protect against pests.
Further research and testing are needed to fully understand and utilize the potential uses of 5-TRIFLUOROMETHOXY-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE, ensuring its safe and effective application in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 877681-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,6,8 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 877681-12:
(8*8)+(7*7)+(6*7)+(5*6)+(4*8)+(3*1)+(2*1)+(1*2)=224
224 % 10 = 4
So 877681-12-4 is a valid CAS Registry Number.
877681-12-4Relevant articles and documents
CYANOPYRROLIDINE DERIVATIVES WITH ACTIVITY AS INHIBITORS OF USP30
-
Page/Page column 61, (2018/06/16)
The present invention relates to a class of substituted-cyanopyrrolidines of Formula (I) with activity as inhibitors of deubiquitilating enzymes, in particular, ubiquitin C-terminal hydrolase 30 or ubiquitin specific peptidase 30 (USP30), having utility i
BENZIMIDAZOLES WITH A HETERO SPIRO-DECANE RESIDUE AS NPY-Y5 ANTAGONISTS
-
, (2008/12/08)
The present invention relates to compounds of formula (I), or a pharmaceutically acceptable salts, solvates, stereoisomers thereof, formula (I), R1 may be C1-C4 alkyl, aryl or heteroaryl, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano; R2 may be halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano, nitro; or aryl, heteroaryl or heterocycle, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano; or R2 may correspond to -0-R3; R3 is a 6-membered aromatic carbocyclic ring which may contain 1 or 2 nitrogen X is carbon or oxygen; Z is carbon or nitrogen; G is a fused 6-membered aromatic carbocyclic ring which may contain 1 or 2 nitrogen; m may be 0 or an integer ranging from 1 to 4; processes for their preparation, intermediates used in these processes, pharmaceutical compositions containing them and their use in therapy, as NPY- Y5 receptor antagonists.
