1283595-65-2 Usage
Chemical structure
1-methyl-2-(2-oxazolyl)-1H-Benzimidazole
Classification
Benzimidazole anthelmintic drug
Function
Treats parasitic worm infections
Target parasites
Pinworm, roundworm, whipworm, and hookworm
Mechanism of action
Inhibits the polymerization of tubulin
Effect on parasites
Disrupts the functioning of microtubules, leading to death
Administration route
Oral
Absorption
Well-absorbed in the gastrointestinal tract
Safety and efficacy
Considered safe and effective with few reported side effects
Drug interactions
May interact with certain medications
Caution
Should be used with caution in individuals with liver disease
Check Digit Verification of cas no
The CAS Registry Mumber 1283595-65-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,3,5,9 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1283595-65:
(9*1)+(8*2)+(7*8)+(6*3)+(5*5)+(4*9)+(3*5)+(2*6)+(1*5)=192
192 % 10 = 2
So 1283595-65-2 is a valid CAS Registry Number.
1283595-65-2Relevant articles and documents
Palladium-catalyzed dehydrogenative cross-couplings of benzazoles with azoles
Han, Wei,Mayer, Peter,Ofial, Armin R.
supporting information; experimental part, p. 2178 - 2182 (2011/04/17)
Different enough: Palladium-catalyzed cross-couplings of benzazoles with imidazoles, oxazoles, and thiazoles furnish unsymmetrical 2,2′- bisheteroaryls in high yield (see scheme). These oxidative Ci-C bond formations use the selective cleavage of the Ci-H bond at C2 in the two coupling partners and are robust enough to be conducted under normal air atmosphere.
