2281-78-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
It is a chemical compound derived from urea, which is an organic compound with the formula NH2CONH2.
Explanation
It is commonly used in the agriculture industry to control the growth of unwanted plants.
Explanation
The chemical works by disrupting the electron transport process in the photosynthetic system II of target plants, leading to their eventual death.
Explanation
It is effective against a wide range of weeds, making it a versatile herbicide.
Explanation
It is frequently combined with other herbicides to enhance its effectiveness in controlling various types of weeds.
Explanation
The chemical can be harmful to aquatic life, so care should be taken to minimize its impact on water bodies.
Explanation
If not handled and used correctly, the chemical can pose risks to human health, so proper safety measures should be followed.
Derivative of urea
Yes
Application
Herbicide in agriculture
Mode of action
Inhibits photosynthetic system II electron transport
Effectiveness
Broad spectrum
Combination use
Often used with other herbicides
Toxicity
Toxic to aquatic organisms
Human health risk
Adverse effects if not used properly
Check Digit Verification of cas no
The CAS Registry Mumber 2281-78-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,8 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2281-78:
(6*2)+(5*2)+(4*8)+(3*1)+(2*7)+(1*8)=79
79 % 10 = 9
So 2281-78-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H13ClN2O3S/c1-7(2)12-10(14)13-17(15,16)9-5-3-8(11)4-6-9/h3-7H,1-2H3,(H2,12,13,14)
2281-78-9Relevant articles and documents
A facile synthesis of sulfonylureas: Via water assisted preparation of carbamates
Tanwar, Dinesh Kumar,Ratan, Anjali,Gill, Manjinder Singh
, p. 4992 - 4999 (2017/07/11)
A novel and simple approach to the synthesis of sulfonylureas has been reported. It involved the reaction of various amines with diphenyl carbonate to yield the corresponding carbamates, which subsequently reacted with different sulphonamides to produce different sulfonylureas in excellent yields. The first reaction of diphenyl carbonate with amines was carried out in aqueous:organic (H2O:THF, 90:10) medium at room temperature to produce carbamates that paved a straightforward route to sulfonylureas after reaction with sulfonamides. The above process avoided traditional multistep protocols and the use of hazardous, irritant, toxic and moisture sensitive reagents such as phosgene, isocyanates and/or chloroformates.
