1050886-21-9 Usage
Type of compound
Oxime derivative
Parent compound
1-(4-difluoromethoxy-3-methoxy-phenyl)-ethanone
Structural feature
Contains a nitrogen-oxygen double bond
Potential applications
Medicinal chemistry and pharmaceutical research
Biological activity
Can reactivate organophosphate-inhibited acetylcholinesterase enzymes
Substituents
Difluoromethoxy and methoxy groups on the phenyl ring
Electronic properties
Influenced by difluoromethoxy and methoxy substituents
Steric properties
Influenced by difluoromethoxy and methoxy substituents
Further research
Necessary to explore potential uses and properties
Check Digit Verification of cas no
The CAS Registry Mumber 1050886-21-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,0,8,8 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1050886-21:
(9*1)+(8*0)+(7*5)+(6*0)+(5*8)+(4*8)+(3*6)+(2*2)+(1*1)=139
139 % 10 = 9
So 1050886-21-9 is a valid CAS Registry Number.
1050886-21-9Relevant articles and documents
Synthesis of benzylaminopyrimidines and their fungicidal activities against wheat brown rust and barley powdery mildew
Yamanaka,Moritomo,Fujii,Tanaka,Fukuda,Nishimura
, p. 223 - 229 (2007/10/03)
Members of a new class of fungicide containing benzyl-aminopyrimidine as a core structure were synthesized and their fungicidal potencies against wheat brown rust, Puccinia recondita, and barley powdery mildew, Erysiphe graminis, were assessed. Among these fungicides, N-(fluoroalkoxy or fluorophenoxybenzyl)-4-pyrimidinamines showed notable preventive activities. The potency of the new pyrimidines was increased when a difluoromethoxy or tetrafluorophenoxy group was introduced at the 4- or 3-position of the phenyl moiety and a methyl or ethyl group was introduced at the benzyl position. Structure-activity relationships are discussed.
