54610-73-0

Basic information

• Product Name: 2-FURANCARBOXIMIDAMIDE
• Synonyms: 2-FURANCARBOXIMIDAMIDE;2-Furancarboximidamide(9CI);2-furancarboximidamide(SALTDATA: HCl);furan-5-carboxamidine
• CAS NO: 54610-73-0
• Molecular Formula: C₅H₆N₂O
• Molecular Weight: 110.11
• Product Categories: AMIDINE
• Mol File: 54610-73-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 178.9°C at 760 mmHg
• Flash Point: 62°C
• Appearance: /
• Density: 1.3g/cm³
• Vapor Pressure: 0.965mmHg at 25°C
• Refractive Index: 1.585
• PKA: 11.48±0.40(Predicted)
• CAS DataBase Reference: 2-FURANCARBOXIMIDAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-FURANCARBOXIMIDAMIDE(54610-73-0)
• EPA Substance Registry System: 2-FURANCARBOXIMIDAMIDE(54610-73-0)

Safety Data

• Hazardous Substances Data: 54610-73-0(Hazardous Substances Data)

Usage

General Description

2-Furancarboximidamide, also known as furamid or N,N'-di-o-tolylurea, is a chemical compound used as a pesticide, specifically as a bird repellent. It is a white, odorless powder that is not soluble in water. 2-Furancarboximidamide is toxic to aquatic organisms and has been shown to have a harmful effect on honeybees. It is classified as a hazardous substance and should be handled with care. This chemical is commonly used in agriculture to protect crops from birds, and precautions should be taken to minimize its impact on the environment and non-target organisms.

InChI:InChI=1/C5H6N2O/c6-5(7)4-2-1-3-8-4/h1-3H,(H3,6,7)

Upstream product

• 617-90-3 2-furancarbonitrile 
• 54610-51-4 Furan-2-carboximidsaeure-aethylester-hydrochlorid 

Downstream Products

• 27568-26-9 2-furan-2-yl-5-phenyl-pyrimidine 
• 35345-16-5 2-furan-2-yl-4-(4-nitro-phenyl)-1⁽³⁾H-imidazole 
• 35345-14-3 4-(4-bromo-phenyl)-2-furan-2-yl-1⁽³⁾H-imidazole 
• 35345-10-9 2-furan-2-yl-4-methyl-1(3)H-imidazole 
• 29916-33-4 2-(furan-2-yl)-4,5-diphenyl-1H-imidazole 
• 27110-82-3 2-(furan-2-yl)pyrimidine 
• 104615-18-1 9-chloro-2-(2-furanyl)-[1,2,4]triazolo[1,5-C]quinazolin-5-amine 
• 3878-19-1 fuberidazole 
• 3688-57-1 N²-Phenylfuran-2-carboximidamide 
• 27568-58-7 1-[2-(5-nitro-furan-2-yl)-pyrimidin-5-yloxy]-2-(toluene-4-sulfonyloxy)-ethane 
• 23352-32-1 2-(5-nitro-furan-2-yl)-5-phenyl-pyrimidine 
• 67945-78-2 (α-amino-furfurylidene)-malononitrile 
• 59918-48-8 3,6-di(furan-2-yl)-1,2,4,5-tetrazine 

Relevant articles and documents

Synthesis of ultrahighly electron-deficient pyrrolo[3,4- d ]pyridazine-5,7-dione by inverse electron demand diels-alder reaction and its application as electrochromic materials

A new electron acceptor 6-alkylpyrrolo[3,4-d]pyridazine-5,7-dione (PPD) with a very low LUMO level has been synthesized via a challenging inverse electron demand Diels-Alder reaction between thiophene and furan-decorated tetrazine substrates and an electron-deficient 1-alkyl-1H-pyrrole-2,5-dione unit. The PPD monomer has been incorporated into a series of donor-acceptor-type conjugated polymers as electrochromic materials with good optical contrast, fast switching speed, and high coloration efficiency.

DIPEPTIDYL PEPTIDASE-IV INHIBITING COMPOUNDS, METHODS OF PREPARING THE SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME AS AN ACTIVE AGENT

The present invention relates to novel compounds exhibiting good inhibitory activity versus Dipeptidyl Peptidase-IV(DPP-IV), methods of preparing the same and pharmaceutical compositions containing the same as an active agent.