7462-17-1 Usage
Chemical Class
The compound belongs to the class of acetamides.
Functional Groups
It contains the functional groups chlorophenyl, hydroxyethyl, and acetamide.
Usage
It is commonly used as a herbicide to selectively control weeds in various crops.
Mechanism of Action
It works by interfering with the growth of the weed plants, ultimately leading to their death.
Mammalian and Avian Toxicity
It has been found to have low toxicity towards mammals and birds.
Industrial Applications
It is also used in the pharmaceutical industry for its potential medicinal properties.
Versatility
2-(4-chlorophenoxy)-N-(2-hydroxyethyl)acetamide is a versatile compound with applications in both agriculture and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 7462-17-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7462-17:
(6*7)+(5*4)+(4*6)+(3*2)+(2*1)+(1*7)=101
101 % 10 = 1
So 7462-17-1 is a valid CAS Registry Number.
7462-17-1Relevant academic research and scientific papers
CONJUGATES OF AUXIN ANALOGS
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Page/Page column 49; 50, (2020/10/28)
Described herein are methods of enhancing formation and/or growth of an adventitious root in a plant and/or plant tissue, and/or for promoting grafting unification, enhancing fruit size and/or reducing flowering in a plant. The method comprises contacting
Alkoxide-Accelerated Smiles Rearrangements. Synthesis of N-(2-Hydroxyethyl)anilines from N-(2-Hydroxyethyl)(aryloxy)acetamides
Baker, William R.
, p. 5140 - 5143 (2007/10/02)
The first example of an alkoxide-accelerated Smiles rearrangement is reported.The rearrangement of N-(2-hydroxyethyl)(aryloxy)acetamides in dimethylformamide or tetrahydrofuran-18-crown-6 and potassium hydride produces useful yields of substituted N-(2-hydroxyethyl)anilines.
