26172-44-1

Basic information

• Product Name: 2-furoylisothiocyanate
• Synonyms: 2-furoylisothiocyanate
• CAS NO: 26172-44-1
• Molecular Weight: 153.161
• Mol File: 26172-44-1.mol
• Article Data: 44

Chemical Properties

• CAS DataBase Reference: 2-furoylisothiocyanate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-furoylisothiocyanate(26172-44-1)
• EPA Substance Registry System: 2-furoylisothiocyanate(26172-44-1)

Safety Data

• Hazardous Substances Data: 26172-44-1(Hazardous Substances Data)

Upstream product

• 527-69-5 2-furancarbonyl chloride 
• 88-14-2 2-furanoic acid 
• 452-58-4 2,3-Diaminopyridine 
• 540-72-7 sodium thiocyanide 
• 1147550-11-5 ammonium thiocyanate 
• 333-20-0 potassium thioacyanate 
• 592-87-0 lead(II) thiocyanate 

Downstream Products

• 166274-70-0 Furan-2-carboxylic acid {N'-[2-(4-chloro-phenoxy)-acetyl]-hydrazinocarbothioyl}-amide 
• 166274-73-3 Furan-2-carboxylic acid [N'-(2-phenoxy-acetyl)-hydrazinocarbothioyl]-amide 
• 166274-76-6 Furan-2-carboxylic acid {N'-[2-(3-nitro-phenoxy)-acetyl]-hydrazinocarbothioyl}-amide 
• 166274-75-5 Furan-2-carboxylic acid {N'-[2-(2-nitro-phenoxy)-acetyl]-hydrazinocarbothioyl}-amide 
• 166274-74-4 Furan-2-carboxylic acid {N'-[2-(4-nitro-phenoxy)-acetyl]-hydrazinocarbothioyl}-amide 
• 166274-69-7 Furan-2-carboxylic acid [N'-(2-o-tolyloxy-acetyl)-hydrazinocarbothioyl]-amide 
• 166274-68-6 Furan-2-carboxylic acid [N'-(2-p-tolyloxy-acetyl)-hydrazinocarbothioyl]-amide 
• 166274-72-2 Furan-2-carboxylic acid {N'-[2-(4-methoxy-phenoxy)-acetyl]-hydrazinocarbothioyl}-amide 
• 82755-20-2 1-furoyl-3-(o-chlorophenyl)thiourea 
• 27349-25-3 5-furan-2-yl-2-phenyl-2,4-dihydro-[1,2,4]triazole-3-thione 
• 952614-77-6 {2-[4-(furan-2-carbonyl)-piperazin-1-yl]-4-furan-2-yl-thiazol-5-yl}-p-tolyl-methanone 

Relevant articles and documents

New N-(1,3,4-thiadiazol-2-yl)furan-2-carboxamide derivatives as potential inhibitors of the VEGFR-2

The present study reports the synthesis and biological evaluation of a new series of novel N-(1,3,4-thiadiazol-2-yl)furan-2-carboxamide derivatives. The reactions were executed under both conventional and microwave irradiation conditions. An enhancement i

Tunable Anticancer Activity of Furoylthiourea-Based RuII–Arene Complexes and Their Mechanism of Action

Fourteen new RuII–arene (p-cymene/benzene) complexes (C1–C14) have been synthesized by varying the N-terminal substituent in the furoylthiourea ligand and satisfactorily characterized by using analytical and spectroscopic techniques. Electrosta

O-benzyl-N-(2-furoyl)thiocarbamate

The O-benzyl-N-(2-furoyl)thiocarbamate (1) was obtained by direct reaction between furoyl isothiocyanate and benzyl alcohol. The X-ray diffraction analysis of 1 showed an orthorhombic system, with a = 7.811(4) A, b = 9.685(4) A, c = 33.562(15) A, and spac

Highly active copper(i) complexes of aroylthiourea ligands against cancer cells-synthetic and biological studies

The reaction of copper(i) bromide with aroylthiourea ligands (L) in the molar ratio 1?:?3 resulted in the formation of [CuBr(L)3]. The complexes were well characterized by analytical and spectroscopic (UV-visible, FT-IR, NMR and mass) technique

Electrochemical sensing of doxepin using acylthiourea-modified glassy carbon electrode

Acylthiourea (ATU) compounds 4-(3-(furan-2-carbonyl)thioureido)benzoic acid (1), 4-(3-(thiophene-2-carbonyl)thioureido)benzoic acid (2), and 4-(3-(benzoyl)thioureido)benzoic acid (3) were synthesized and characterized by NMR (1H and 13/su