14676-37-0 Usage
Synthetic organic compound
It is a man-made chemical substance that is created through chemical synthesis, as opposed to being derived from natural sources.
Derivative of acetamide
2,2-dichloro-N-(2-methoxyphenyl)acetamide is derived from acetamide, which is a simple organic compound with the molecular formula CH3CONH2.
Two chlorine atoms
The compound has two chlorine atoms (Cl) attached to the molecule, which contributes to its insecticidal and herbicidal properties.
Methoxyphenyl group
A methoxy group (-OCH3) is attached to the phenyl ring (a six-carbon ring structure with alternating single and double bonds) in the compound, further enhancing its effectiveness as an insecticide and herbicide.
Insecticide and herbicide
The compound is commonly used in agriculture to control pests (insects) and unwanted vegetation (weeds) by disrupting the nervous system of insects and inhibiting the growth of weeds.
Toxic to aquatic organisms
The chemical can be harmful to aquatic life, such as fish and other water-dwelling creatures, making it important to use and dispose of it responsibly.
Potential risks to human health and the environment
Due to its toxic nature, improper handling and disposal of 2,2-dichloro-N-(2-methoxyphenyl)acetamide can pose risks to human health and the environment.
Proper handling and disposal
To prevent harmful effects, it is essential to follow safety guidelines and regulations when using, storing, and disposing of this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 14676-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14676-37:
(7*1)+(6*4)+(5*6)+(4*7)+(3*6)+(2*3)+(1*7)=120
120 % 10 = 0
So 14676-37-0 is a valid CAS Registry Number.
14676-37-0Relevant articles and documents
Approach for the direct synthesis of β-dichlorosubstituted acetanilides using iodine trichloride (ICl3) as the oxidant and catalyst
Zhang, Qing,Liu, Weibing,Chen, Cui,Tan, Liquan
, p. 453 - 455 (2013)
A reliable method for direct synthesis of β-dichlorosubstituted acetanilides is reported. The key transformation involves the oxidative and catalytic cleavage of a carbon-carbon bond in the presence of iodine trichloride (ICl3). In this protoco
Organic synthesis using (diacetoxyiodo)benzene (DIB): Unexpected and novel oxidation of 3-oxobutanamides to 2,2-dihalo-N-phenylacetamides
Liu, Wei-Bing,Chen, Cui,Zhang, Qing,Zhu, Zhi-Bo
supporting information; experimental part, p. 344 - 348 (2012/05/04)
A novel and reliable method for the direct preparation of 2,2-dihalo-N-phenylacetamides is reported. The key transformation involves the cleavage of a carbon-carbon bond in the presence of DIB and a Lewis acid as the halogen source, and thus this method s
