80282-49-1

Basic information

• Product Name: 1-(1-(2-hydroxyphenyl)-2-methanone)-1H-imidazole
• Synonyms: 1-(1-(2-hydroxyphenyl)-2-methanone)-1H-imidazole
• CAS NO: 80282-49-1
• Molecular Weight: 188.186
• Mol File: 80282-49-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-(1-(2-hydroxyphenyl)-2-methanone)-1H-imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-(2-hydroxyphenyl)-2-methanone)-1H-imidazole(80282-49-1)
• EPA Substance Registry System: 1-(1-(2-hydroxyphenyl)-2-methanone)-1H-imidazole(80282-49-1)

Safety Data

• Hazardous Substances Data: 80282-49-1(Hazardous Substances Data)

Upstream product

• 288-32-4 1H-imidazole 
• 1441-87-8 salicyloyl chloride 
• 69-72-7 salicylic acid 
• 530-62-1 1,1'-carbonyldiimidazole 

Downstream Products

• 1469-94-9 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanedione 
• 138206-46-9 (E)-1-<1-(2-Hydroxyphenyl)-2-(methylthio)ethenyl>-1H-imidazole 
• 130773-02-3 (E)-1-[2-methylthio-1-[2-(pentyloxy)phenyl]ethenyl]-1H-imidazole hydrochloride 
• 1092940-82-3 2-azido-5'-O-[N-(2-hydroxybenzoyl)sulfamoyl]-2',3'-O-isopropylideneadenosine triethylammonium 
• 80282-50-4 ethyl thiosalicylate 
• 67410-90-6 2-hydroxy-N-(7-oxa-3-thia-1-aza-spiro[5.5]undec-1-en-2-yl)-benzamide 

Relevant articles and documents

Actinide sequestration using self-assembled monolayers on mesoporous supports

Surfactant templated synthesis of mesoporous ceramics provides a versatile foundation upon which to create high efficiency environmental sorbents. These nanoporous ceramic oxides condense a huge amount of surface area into a very small volume. The ceramic

Study of the Reaction of Hydroxybenzoyl Chlorides and Their Derivatives with Imidazole

The reaction of hydroxybenzoyl chlorides with imidazole was studied on an example of the Schotten-Baumann reaction of salicyloyl and acetylsalicyloyl chlorides with imidazole, which, according to soe published data, can take two different ways. It was sho

Chiral sulfinamide ligand as well as preparation method and application of chiral sulfinamide ligand

The invention relates to a chiral sulfinamide ligand as well as a preparation method and application of the chiral sulfinamide ligand. The ligand is further applied to asymmetric allylation reaction catalyzed by metal palladium. In dried tetrahydrofuran,