56836-51-2

Basic information

• Product Name: Carbamic acid, (2-hydroxyphenyl)-, ethyl ester
• CAS NO: 56836-51-2
• Molecular Formula: C9H11NO3
• Molecular Weight: 181.191
• Mol File: 56836-51-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Carbamic acid, (2-hydroxyphenyl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (2-hydroxyphenyl)-, ethyl ester(56836-51-2)
• EPA Substance Registry System: Carbamic acid, (2-hydroxyphenyl)-, ethyl ester(56836-51-2)

Safety Data

• Hazardous Substances Data: 56836-51-2(Hazardous Substances Data)

Upstream product

• 6132-42-9 o-nitrophenyl ethyl carbonate 
• 541-41-3 chloroformic acid ethyl ester 
• 95-55-6 2-amino-phenol 
• 19213-72-0 ethyl 1-imidazolecarboxylate 
• 15062-88-1 2-hydrazino-1,3-benzoxazole 
• 64-17-5 ethanol 
• 17280-90-9 2-oxo-benzooxazole-3-carboxylic acid ethyl ester 
• 101-99-5 N-carboethoxyaniline 
• 62-53-3 aniline 
• 88-75-5 2-hydroxynitrobenzene 
• 123-54-6 acetylacetone 

Downstream Products

• 35601-91-3 ethyl N-(o-methoxyphenyl) carbamate 
• 64-17-5 ethanol 
• 124-38-9 carbon dioxide 
• 95-55-6 2-amino-phenol 
• 376592-93-7 3′-amino-2′-hydroxy biphenyl-3-carboxylic acid 
• 5466-88-6 3,4-dihydro-3-oxo-2H-1,4-benzoxazine 
• 83855-47-4 [2-(2-Hydroxy-3-isopropylamino-propoxy)-phenyl]-carbamic acid ethyl ester 
• 52134-40-4 [2-(3-tert-Butylamino-2-hydroxy-propoxy)-phenyl]-carbamic acid ethyl ester 
• 871883-12-4 1-ethoxycarbonyloxy-2-butoxycarbonylamino-benzene 
• 52134-45-9 (2-Oxiranylmethoxy-phenyl)-carbamic acid ethyl ester 
• 17280-90-9 2-oxo-benzooxazole-3-carboxylic acid ethyl ester 
• 38191-26-3 4-(2-hydroxy-phenyl)-semicarbazide 
• 59-49-4 2-Benzoxazolinone 
• 132887-16-2 [2-(2-morpholino-ethoxy)-phenyl]-carbamic acid ethyl ester; hydrochloride 

Relevant articles and documents

Palladium catalyzed Csp2-H activation for direct aryl hydroxylation: The unprecedented role of 1,4-dioxane as a source of hydroxyl radicals

A novel strategy for direct aryl hydroxylation via Pd-catalysed Csp2-H activation through an unprecedented hydroxyl radical transfer from 1,4-dioxane, used as a solvent, is reported with bio relevant and sterically hindered heterocycles and various acyclic functionalities as versatile directing groups.

General and efficient synthesis of benzoxazol-2(3H)-ones: Evolution of their anti-cancer and anti-mycobacterial activities

A novel class of benzo[d]oxazol-2(3H)-one derivatives has been synthesized and their in vitro cytotoxicity against human pancreatic adenocarcinoma and human non-small cell lung carcinoma cancer cell lines was evaluated. Many of these compounds were found to display excellent to moderate activity. Among them, 6b, 6l, 6n and 6x were identified as lead molecules. In particular, 6l and 6n were found to be potent against the pancreatic adenocarcinoma cell line whereas the 6x was found to be effective against the human non-small cell lung carcinoma cell line. Conversely, the compounds 6l-x were found to be ineffective against Mycobacterium tuberculosis. Of the various molecules, 6h showed promising anti-mycobacterial activity, with an IC50 value equal to that of ciprofloxacin.

Synthesis of Carbamates Using Yttria-Zirconia Based Lewis Acid Catalyst

A variety of amines react with chloroformates in the presence of catalytic amount of yttria-zirconia based catalyst to afford the corresponding carbamates in excellent yields.