175205-63-7 Usage
General Description
3-Chloromethyl-5-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole is a chemical compound with the molecular formula C9H6ClF3N2O. It is a heterocyclic compound containing an oxadiazole ring with a chloromethyl and a trifluoromethylphenyl group attached to it. 3-Chloromethyl-5-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole has various potential applications in the fields of pharmaceuticals, agrochemicals, and materials science due to its diverse biological and chemical properties. It can be used as a building block for the synthesis of new drugs, agrochemicals, and materials with desired properties. Additionally, it exhibits potential biological activities such as antifungal, antibacterial, antiviral, and anticancer properties, making it a promising candidate for drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 175205-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,0 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 175205-63:
(8*1)+(7*7)+(6*5)+(5*2)+(4*0)+(3*5)+(2*6)+(1*3)=127
127 % 10 = 7
So 175205-63-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO3/c1-2-10-6(8)5-3-9-4-7-5/h3-4H,2H2,1H3
175205-63-7Relevant articles and documents
Novel 1,3-dipropyl-8-(1-heteroarylmethyl-1H-pyrazol-4-yl)-xanthine derivatives as high affinity and selective A2B adenosine receptor antagonists
Elzein, Elfatih,Kalla, Rao,Li, Xiaofen,Perry, Thao,Parkhill, Eric,Palle, Venkata,Varkhedkar, Vaibahv,Gimbel, Art,Zeng, Dewan,Lustig, David,Leung, Kwan,Zablocki, Jeff
, p. 302 - 306 (2007/10/03)
A series of new 1,3-dipropyl-8-(1-heteroarylmethyl-1H-pyrazol-4-yl)- xanthine derivatives as A2B-AdoR antagonists have been synthesized and evaluated for their binding affinities for the A2B, A 1, A2A, and A3-AdoRs. 8-(1-((3-phenyl-1,2,4- oxadiazol-5-yl)methyl)-1H-pyrazol-4-yl)-1,3-dipropyl-1H-purine-2,6(3H,7H)-dione (4) displayed high affinity (Ki = 1 nM) and selectivity for the A2B-AdoR versus A1, A2A, and A 3-AdoRs (A1/A2B, A2A/A2B, and A3/A2B selectivity ratios of 370, 1100, and 480, respectively). The synthesis and SAR of this novel class of compounds are presented herein.