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dl-5-Chloro-6-methyl-4-(α-methyl-4-difluoromethoxybenzyl-amino)pyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130362-01-5

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130362-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130362-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,3,6 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 130362-01:
(8*1)+(7*3)+(6*0)+(5*3)+(4*6)+(3*2)+(2*0)+(1*1)=75
75 % 10 = 5
So 130362-01-5 is a valid CAS Registry Number.

130362-01-5Relevant academic research and scientific papers

Quantitative structure-fungicidal activity relationships of N-(4- difluoromethoxybenzyl)pyrimidin-4-amines against wheat and barley fungi

Yamanaka,Moritomo,Fujii,Tanaka,Fukuda,Nishimura

, p. 896 - 902 (2007/10/03)

A set of N-(4-difluoromethoxybenzyl)pyrimidinamines with various substituents at the 4- and 5-positions of the pyrimidine ring and at the benzyl position were prepared, and their fungicidal activities against wheat brown rust, Puccinia recondita, and barley powdery mildew, Erisiphe graminis, were measured. Variations in each of these activities were quantitatively analysed by the use of physicochemical substituent parameters and a regression analysis. Each of these activities was parabolically correlated with the steric bulkiness of the pyrimidine substituents and with the bulkiness or the hydrophobicity of the benzylic substituents.

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.

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