41191-04-2 Usage
Description
Triazinate is a class of selective herbicides that contain the active ingredient atrazine, a broad-spectrum herbicide known for its effectiveness and persistence in the environment. It is commonly used to control broadleaf and grassy weeds in agricultural crops, turf, and non-crop areas by inhibiting the photosynthesis process in susceptible plants, leading to the death of the targeted weeds.
Uses
Used in Agricultural Industry:
Triazinate is used as a selective herbicide for controlling broadleaf and grassy weeds in agricultural crops. It is effective in managing weed growth, thereby improving crop yield and quality.
Used in Turf and Non-Crop Areas:
Triazinate is used as a weed control agent in turf and non-crop areas to maintain a clean and healthy environment. Its selective action ensures that only the targeted weeds are eliminated, preserving the desired vegetation.
Despite the effectiveness and cost efficiency of Triazinate, it has been linked to some environmental and health concerns, leading to restrictions on its use in certain regions. However, it continues to be widely used in weed control due to its proven benefits in managing weed growth and improving the overall health of the areas it is applied to.
Check Digit Verification of cas no
The CAS Registry Mumber 41191-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,9 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41191-04:
(7*4)+(6*1)+(5*1)+(4*9)+(3*1)+(2*0)+(1*4)=82
82 % 10 = 2
So 41191-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H25ClN6O2/c1-21(2)26-19(23)25-20(24)28(21)15-8-9-17(16(22)11-15)30-12-13-6-5-7-14(10-13)18(29)27(3)4/h5-11H,12H2,1-4H3,(H4,23,24,25,26)
41191-04-2Relevant articles and documents
Metal-Free Amidation of Acids with Formamides and T3P
Bannwart, Linda,Abele, Stefan,Tortoioli, Simone
, p. 2069 - 2078 (2016/07/06)
A new, simple and metal-free method for the direct formation of dialkylamides from carboxylic acids employing N,N-dialkylformamides as amine source is described. The one-pot reaction is promoted by propylphosphonic anhydride (T3P) in the presence of 0.5 equivalents of HCl.
