104098-48-8 | Imazapic

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$58.00	$40.00
500mg	95%	in stock	$115.00	$80.00

Description

• Catalog Number: AX19992
• Chemical Name: Imazapic
• CAS Number: 104098-48-8
• Molecular Formula: C14H17N3O3
• Molecular Weight: 275.3031
• MDL Number: MFCD04307828
• SMILES: Cc1cnc(c(c1)C(=O)O)C1=NC(C(=O)N1)(C)C(C)C

Computed Properties

• Complexity: 461
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 20
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.6

Upstream Synthesis Route

Imazapic is widely utilized in chemical synthesis as a potent herbicide, specifically belonging to the imidazolinone family. Its chemical structure enables it to selectively target broadleaf weeds and grasses, making it a highly effective tool for weed control in agricultural settings. In organic synthesis, Imazapic is commonly employed for the preparation of various herbicidal formulations and can be utilized to create custom herbicide blends with specific target properties. Its ability to inhibit the growth of unwanted plant species while being relatively safe for desired crops makes Imazapic a valuable tool in modern agricultural practices. Additionally, its selective mode of action and environmentally friendly profile further enhance its appeal in chemical synthesis applications.

Literature

• 2-(4-Isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-methyl-nicotinic acid.

  Acta crystallographica. Section E, Structure reports online 20120601

• Toxicological responses of Cyprinus carpio after exposure to a commercial herbicide containing imazethapyr and imazapic.

  Ecotoxicology and environmental safety 20110301

• Bioavailability of diuron, imazapic and isoxaflutole in soils of contrasting textures.

  Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes 20091101

• Photolysis pathway of imazapic in aqueous solution: ultrahigh resolution mass spectrometry analysis of intermediates.

  Journal of agricultural and food chemistry 20071128

• Cross-resistance to imidazolinone herbicides in chlorsulfuron-resistant Raphanus raphanistrum.

  Pest management science 20020901