149774-14-1 Usage
Chemical class
Oxime
Derived from
4-difluoromethoxy-phenyl moiety and ethanone
Potential applications
Pharmaceutical and medicinal chemistry
Interaction with biological targets
Yes
Chemical structure
Contains an oxime functional group
Coordination chemistry
Can form stable complexes with metal ions
Metal-based pharmaceuticals
Useful in the development of
Biological activities
Potential (may serve as a precursor for the synthesis of bioactive compounds)
These properties and contents are based on the information provided in the material, which highlights the chemical class, common name, derivation, potential applications, interaction with biological targets, chemical structure, coordination chemistry, and potential biological activities of DFMO-oxime.
Check Digit Verification of cas no
The CAS Registry Mumber 149774-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,7,7 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 149774-14:
(8*1)+(7*4)+(6*9)+(5*7)+(4*7)+(3*4)+(2*1)+(1*4)=171
171 % 10 = 1
So 149774-14-1 is a valid CAS Registry Number.
149774-14-1Relevant 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.
