1020325-22-7 Usage
Description
BenzeneMethanol, 3-[[5-(trifluoroMethyl)-2-pyridinyl]oxy]is a chemical compound that features a benzene ring connected to a methanol molecule, with a 3-[[5-(trifluoroMethyl)-2-pyridinyl]oxy] side chain. BenzeneMethanol, 3-[[5-(trifluoroMethyl)-2-pyridinyl]oxy]is known for its potential applications in the pharmaceutical industry and as a possible antiviral and antifungal agent.
Uses
Used in Pharmaceutical Industry:
BenzeneMethanol, 3-[[5-(trifluoroMethyl)-2-pyridinyl]oxy]is utilized as an intermediate in the synthesis of various drugs and other organic compounds, playing a crucial role in the development of new medications.
Used in Antiviral Applications:
BenzeneMethanol, 3-[[5-(trifluoroMethyl)-2-pyridinyl]oxy]has been studied for its potential as an antiviral agent, indicating its possible use in combating viral infections and contributing to the development of antiviral medications.
Used in Antifungal Applications:
BenzeneMethanol, 3-[[5-(trifluoroMethyl)-2-pyridinyl]oxy]has also shown promise as an antifungal agent, suggesting its potential use in treating fungal infections and being incorporated into antifungal products.
It is important to handle BenzeneMethanol, 3-[[5-(trifluoroMethyl)-2-pyridinyl]oxy]with care, as it is considered hazardous and may pose risks to human health and the environment if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 1020325-22-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,3,2 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1020325-22:
(9*1)+(8*0)+(7*2)+(6*0)+(5*3)+(4*2)+(3*5)+(2*2)+(1*2)=67
67 % 10 = 7
So 1020325-22-7 is a valid CAS Registry Number.
1020325-22-7Relevant articles and documents
Discovery and evaluation of novel FAAH inhibitors in neuropathic pain model
Bhuniya, Debnath,Kharul, Rajendra K.,Hajare, Atul,Shaikh, Nadim,Bhosale, Sandeep,Balwe, Sandip,Begum, Fouzia,De, Siddhartha,Athavankar, Sonalee,Joshi, Dhananjay,Madgula, Vamsi,Joshi, Kaushal,Raje, Amol A.,Meru, Ashwinkumar V.,Magdum, Amol,Mookhtiar, Kasim A.,Barbhaiya, Rashmi
, p. 238 - 243 (2018/12/05)
Conceptual design and modification of urea moiety in chemotype PF-3845/04457845, the bench marking irreversible inhibitor of fatty acid amide hydrolase (FAAH), led to discovery of a novel nicotinamide-based lead 12a having reversible mechanism of action.
AMIDE COMPOUNDS, COMPOSITIONS AND APPLICATIONS THEREOF
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, (2013/04/10)
The present disclosure relates to substituted amide compounds that are inhibitors of Fatty Acid Amide Hydrolase (FAAH), their stereoisomers, tautomers, prodrugs, polymorphs, solvates, pharmaceutically acceptable salts, and pharmaceutical compositions cont
4- [3- (ARYLOXY) BENZYLIDENE] -3-METHYL PIPERIDINE ARYL CARBOXAMIDE COMPOUNDS USEFUL AS FAAH INHIBITORS
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Page/Page column 24; 25, (2009/12/02)
The present invention relates to compounds of Formula (I), wherein Ar is optionally substituted phenyl or heteroaryl and X, Y and Z are independently N or CH; or a pharmaceutically acceptable salt thereof; processes for the preparation of the compounds; intermediates used in the preparation of the compounds; compositions containing the compounds; and uses of the compounds in treating diseases or conditions associated with fatty acid amide hydrolase (FAAH) activity.
