5465-96-3 Usage
Description
2-Nitroaminoimidazoline is an organic compound characterized by its nitroamino and imidazoline functional groups. It is a neonicotinoid substituent known for its ability to form water bridges at the nicotinic acetylcholine receptor, which plays a crucial role in its biological activity.
Uses
Used in Pesticide Industry:
2-Nitroaminoimidazoline is used as an active ingredient in neonicotinoid insecticides for its ability to effectively control a wide range of pests. Its mode of action involves forming water bridges at the nicotinic acetylcholine receptor, leading to paralysis and death of the insects.
Used in Crop Protection:
2-Nitroaminoimidazoline is used as a component in crop protection products to enhance their efficacy against various pests. Its incorporation into these products helps to improve the overall protection of crops, leading to increased yield and reduced damage from insect infestations.
Used in Integrated Pest Management (IPM):
2-Nitroaminoimidazoline is utilized as a part of integrated pest management strategies, where it is combined with other pest control methods such as biological control, cultural practices, and monitoring. This holistic approach aims to reduce the reliance on chemical pesticides and promote sustainable agriculture.
Used in Research and Development:
2-Nitroaminoimidazoline is employed in the research and development of new neonicotinoid insecticides and other related compounds. Its unique properties make it a valuable tool for understanding the mechanisms of action and potential applications in pest control and crop protection.
Check Digit Verification of cas no
The CAS Registry Mumber 5465-96-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5465-96:
(6*5)+(5*4)+(4*6)+(3*5)+(2*9)+(1*6)=113
113 % 10 = 3
So 5465-96-3 is a valid CAS Registry Number.
InChI:InChI=1/C3H6N4O2/c8-7(9)6-3-4-1-2-5-3/h1-2H2,(H2,4,5,6)/p+1
5465-96-3Relevant articles and documents
Quinoline and 2-nitroimino-1, 3-diazacycloalkane hybrids: Design, synthesis and insecticidal activity
Sowmya, Jonnalagadda,Padma, Banda,Leelavathi, Panaganti
, (2021/12/09)
A library of new hybrid molecules comprising quinoline, 2-nitroimino-1, 3-diazacycloalkane motifs were designed and synthesized as plausible neonicotinoid analogues. These compounds were synthesized from 2-chloro/aryloxy-3-formyl quinolines and guanidine nitrate with the coupling of 2-chloro/aryloxy-3-(chloromethyl)quinolines, 2-nitroimino-1, 3-diazacycloalkanes under phase transfer catalysis (PTC) as crucial step. All the compounds were obtained in excellent yields (80–90%) and were characterized by 1H, 13C NMR and mass spectrometry. The newly generated compounds were screened for insecticidal activity against aphids in safflower field and some of them displayed moderate activity.
A MANUFACTURING PROCESS FOR 2-NITROIMINO HETEROCYCLIC COMPOUNDS
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Page/Page column 23-26, (2020/04/25)
The present invention relates to a process for manufacture of 2-nitroimino heterocyclic compounds and intermediates thereof. More particularly, the present invention relates to a convenient manufacturing process for preparation of 2-nitroimino imidazolidine compounds.
Efficient synthesis of N-allylated 2-nitroiminoimidazolidine analogues from Baylis–Hillman bromides
Kumar, Sriramoju Bharath,Pavan Kumar, Chebolu Naga Sesha Sai,Santhoshi, Amlipur,Kumar, Koochana Pranay,Murthy,Jayathirtha Rao, Vaidya
supporting information, p. 131 - 136 (2017/01/11)
Various Baylis–Hillman–derived new N-allylated 2-nitroiminoimidazolidine analogs were efficiently prepared using potassium carbonate as base. Simple workup procedure, excellent yields, and mild reaction conditions are the salient features of this method. All the synthesized compounds are screened for their larvicidal activity on fourth instar mosquito larvae, Culex quinquefasciatus.