115540-88-0 Usage
Use
Herbicide for controlling broadleaf weeds and woody plants in agricultural and non-crop areas
Mechanism of action
Inhibits weed growth and interferes with photosynthesis
Stability in soil
Relatively stable
Risk of leaching
Low risk of leaching into groundwater
Toxicity
Toxic to aquatic organisms, may cause skin and eye irritation in humans
Environmental impact
Negative effects on wildlife, may bioaccumulate
Handling and disposal
Proper handling and disposal procedures are necessary
Check Digit Verification of cas no
The CAS Registry Mumber 115540-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,5,4 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 115540-88:
(8*1)+(7*1)+(6*5)+(5*5)+(4*4)+(3*0)+(2*8)+(1*8)=110
110 % 10 = 0
So 115540-88-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H7Cl2NOS/c9-5-2-1-3-6(8(5)10)12-4-7(11)13/h1-3H,4H2,(H2,11,13)
115540-88-0Relevant articles and documents
Synthesis and Antitubercular Activity of 4-(5-Nitro-2-furyl/2-pyrazinyl/1-adamantyl)-2-(alkyl/aryl/arylamino)thiazoles
Khadse, B. G.,Lokhande, S. R.,Bhamaria, R. P.,Prabhu, S. R.
, p. 856 - 860 (2007/10/02)
The reaction of haloketones, obtained from Arndt-Eistert reaction on the acid chlorides of 1-adamantane, 5-nitrofuroic acid and pyrazine-2-carboxylic acid, with different thioamides and thioureas affords the title thiazoles (I-III).Some of them exhibit interesting antitubercular activity at 6.25 to 0.38 μg/ml concentration against H37Rv strain of M. tubercolosis in vitro testing.The structure activity relationship (SAR) has also been discussed.