601513-26-2 Usage
General Description
2-Chloro-4-(trifluoromethyl)phenylacetic acid is a chemical compound with the molecular formula C9H6ClF3O2. It is a derivative of phenylacetic acid and contains a chloro and trifluoromethyl group. 2-CHLORO-4-(TRIFLUOROMETHYL)PHENYLACETIC ACID is used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceuticals. It may also have potential applications in the field of agrochemicals. Due to its unique structure, 2-Chloro-4-(trifluoromethyl)phenylacetic acid has the potential to exhibit diverse chemical and biological properties, making it an interesting target for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 601513-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,1,5,1 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 601513-26:
(8*6)+(7*0)+(6*1)+(5*5)+(4*1)+(3*3)+(2*2)+(1*6)=102
102 % 10 = 2
So 601513-26-2 is a valid CAS Registry Number.
601513-26-2Relevant articles and documents
HETEROCYCLIC AMIDE DERIVATIVES AS P2X7 RECEPTOR ANTAGONISTS
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Page/Page column, (2014/06/24)
The invention relates to heterocyclic amide derivatives of formula (I), wherein R1, R2, R3, R4, R5, X, Y and n are as defined in the description, their preparation and their use as pharmaceutically active compounds.
BICYCLIC PYRIMIDIN-4-(3H)-ONES AND ANALOGUES AND DERIVATIVES THEREOF WHICH MODULATE THE FUNCTION OF THE VANILLOID-1 RECEPTOR (VR1)
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Page/Page column 49, (2010/02/12)
Compounds of formula (I); which are useful as therapeutic compounds, particularly in the treatment of pain and other conditions ameliorated by the modulation of the function of the vanilloid-1 receptor (VR1).
Benzopyrazone compounds, compositions thereof, and methods of treatment therewith
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, (2008/06/13)
Benzopyranone compounds having the following structure: wherein R1, X, Y and n are as defined here, are disclosed. The compounds of formula (I), wherein R1is H, can be prepared by demethylation of the corresponding phenolic methyl et