220239-67-8 Usage
Uses
Used in Pharmaceutical Industry:
2-(Trifluoromethoxy)phenylacetic acid is utilized as a building block in the synthesis of various pharmaceutical compounds for its anti-inflammatory and analgesic properties. It plays a crucial role in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other therapeutic agents, contributing to the treatment of various conditions that require pain relief and inflammation reduction.
Used in Agricultural Applications:
In the agricultural sector, 2-(Trifluoromethoxy)phenylacetic acid has been studied for its potential use as a herbicide. Its application aims to control and manage unwanted plant growth, thereby enhancing crop productivity and quality. 2-(Trifluoromethoxy)phenylacetic acid's effectiveness in this context is under investigation to ensure its safety and efficacy as an agricultural chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 220239-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,2,3 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 220239-67:
(8*2)+(7*2)+(6*0)+(5*2)+(4*3)+(3*9)+(2*6)+(1*7)=98
98 % 10 = 8
So 220239-67-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3O3/c10-9(11,12)15-7-4-2-1-3-6(7)5-8(13)14/h1-4H,5H2,(H,13,14)
220239-67-8Relevant articles and documents
Tocolytic oxytocin receptor antagonists
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, (2008/06/13)
This invention relates to certain novel benzoxazinone compounds and derivatives thereof, their synthesis, and their use as oxytocin receptor antagonists. One application of these compounds is in the treatment of preterm labor in mammals, especially humans. The ability of the compounds to relax uterine contractions in mammals also makes them useful for treating dysmenorrhea and stopping labor prior to cesarean delivery.
PIPERAZINE OXYTOCIN RECEPTOR ANTAGONISTS
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, (2008/06/13)
This invention relates to certain novel piperazine compounds and derivatives thereof, their synthesis, and their use as oxytocin receptor antagonists. One application of these compounds is in the treatment of preterm labor in mammals, especially humans. The ability of the compounds to relax uterine contractions in mammals also makes them useful for treating dysmenorrhea and stopping labor prior to cesarean delivery.