1019372-32-7 Usage
Physical appearance
White crystalline solid The compound forms a white, crystal-like structure when in its solid state.
Solubility
Soluble in organic solvents, insoluble in water The compound dissolves easily in organic solvents but does not dissolve in water.
Usage
Herbicide 2-(3-chlorophenoxy)-3-methylbutanoic acid is commonly used to control broadleaf weeds in various crops.
Selectivity
Selective herbicide The compound specifically targets broadleaf weeds without harming the desired crops.
Mode of action
Inhibits plant growth The herbicide works by inhibiting the growth of targeted plants, making it effective in controlling weeds.
Applications
Agricultural and horticultural The compound is widely used in both agricultural and horticultural settings to manage weeds.
Potency
Potent and effective 2-(3-chlorophenoxy)-3-methylbutanoic acid is considered a strong and efficient herbicide.
Safety precautions
Handle with care, follow safety guidelines Due to its potential toxicity, it is important to handle the compound carefully and use it according to the recommended safety guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 1019372-32-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,9,3,7 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1019372-32:
(9*1)+(8*0)+(7*1)+(6*9)+(5*3)+(4*7)+(3*2)+(2*3)+(1*2)=127
127 % 10 = 7
So 1019372-32-7 is a valid CAS Registry Number.
1019372-32-7Relevant articles and documents
Quantitative structure activity relationship studies in pyrethroid esters derived from substituted 3-methyl-2-phenoxybutanoic acids against Culex quinquefasciatus
Mathew, Nisha,Subramanian,Kalyanasundaram
, p. 40 - 44 (2007/10/03)
QSAR studies in relation to three physicochemical substituent parameters, lipophilicity, electronic and steric factors have been carried out with pyrethroid esters derived from substituted 3-methyl-2-phenoxybutanoic acids against Culex quinquefasciatus applying multiple regression analysis by grouping the esters into three based on their alcohol moiety. In the case of 3-phenoxybenzyl and α-cyano-3-phenoxybenzyl esters the larvicidal activity is mainly influenced by the lipophilic and electronic nature of the substituent at 4-position of the phenyl ring of the acid moiety. For adulticidal activity the lipophilicity of the substituent at 4-position followed by that of the substituents at 2-and 3-positions along with the steric effect are the important factors for 3-phenoxybenzyl and α-cyano-3-phenoxybenzyl esters. The larvicidal and adulticidal activities of 3,4-methylenedioxybenzyl esters are influenced by electronic factor followed by steric effect of the substituent.
