2211-96-3 Usage
Chemical structure
A synthetic organic compound with a triclorophenoxymethyl group attached to an oxirane ring.
Usage
Primarily used as a herbicide to control various types of weeds and woody plants.
Mechanism of action
Disrupts plant growth and causes the plants to die.
Effectiveness
Highly effective in both agricultural and residential settings.
Mammalian toxicity
Considered to have low toxicity to mammals.
Environmental degradation
Rapidly broken down in the environment, reducing its potential for long-term environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 2211-96-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2211-96:
(6*2)+(5*2)+(4*1)+(3*1)+(2*9)+(1*6)=53
53 % 10 = 3
So 2211-96-3 is a valid CAS Registry Number.
2211-96-3Relevant academic research and scientific papers
A NEW APPLICATION OF CORRELATION EQUATIONS. INFLUENCE OF SUBSTITUENT ON BASICITY OF A SERIES OF CHLOROPHENYL GLYCIDYL ETHERS
Stolarzewicz, Andrzej,Dworak, Andrzej,Jedlinski, Zbigniew
, p. 2517 - 2523 (2007/10/02)
The relation between the basicity of simple oxiranes and substituent constants was described earlier by the common equation pKb=co+c1?.It has been shown that this equation is not satisfied in the case of chlorophenyl glycidyl ethers, when the pKa values of chlorophenols have been taken as a measure of the inductive effect of chlorophenoxy substituent and pKb have been estimated from infrared measurements.The modification of the equation to the following form: pKb=co+(c1+c2Sk)pKa by considerarion of the conformation factor Sk make a good correlation possible.The possibility of the existence of some chlorophenyl glycidyl ethers rotameres has been also discussed on the above basis.
