51679-85-7

Basic information

• Product Name: 2-{[ethoxy(oxo)acetyl]amino}benzoic acid
• Synonyms: 2-{[ethoxy(oxo)acetyl]amino}benzoic acid;2-(Ethoxycarbonylcarbonylamino)benzoic acid;2-[(2-ethoxy-1,2-dioxoethyl)amino]benzoic acid;2-[(2-ethoxy-2-keto-acetyl)amino]benzoic acid;2-[(2-ethoxy-2-oxoacetyl)amino]benzoic acid;2-[(2-ethoxy-2-oxo-acetyl)amino]benzoic acid;2-[(2-ethoxy-2-oxo-ethanoyl)amino]benzoic acid;Benzoic acid, 2-((ethoxyoxoacetyl)amino)- (9CI)
• CAS NO: 51679-85-7
• Molecular Formula: C₁₁H₁₁NO₅
• Molecular Weight: 237.21
• Mol File: 51679-85-7.mol
• Article Data: 14

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.382g/cm³
• Refractive Index: 1.597
• CAS DataBase Reference: 2-{[ethoxy(oxo)acetyl]amino}benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{[ethoxy(oxo)acetyl]amino}benzoic acid(51679-85-7)
• EPA Substance Registry System: 2-{[ethoxy(oxo)acetyl]amino}benzoic acid(51679-85-7)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 51679-85-7(Hazardous Substances Data)

Usage

General Description

2-{[ethoxy(oxo)acetyl]amino}benzoic acid is a chemical compound with the molecular formula C13H13NO5. It is a derivative of benzoic acid, with an ethoxy(oxo)acetylamine group attached to the benzene ring. 2-{[ethoxy(oxo)acetyl]amino}benzoic acid is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. It is also known for its anti-inflammatory and analgesic properties, making it a potential candidate for the development of new drugs. The ethoxy(oxo)acetylamine group contributes to the compound's reactivity and ability to form new chemical bonds, making it valuable for a variety of chemical reactions and applications.

InChI:InChI=1/C11H11NO5/c1-2-17-11(16)9(13)12-8-6-4-3-5-7(8)10(14)15/h3-6H,2H2,1H3,(H,12,13)(H,14,15)

Upstream product

• 144-62-7 oxalic acid 
• 118-92-3 anthranilic acid 
• 95-92-1 oxalic acid diethyl ester 
• 70258-72-9 2-ethoxycarbonyl-1,2-dihydroindol-3-one 
• 18631-77-1 2-hydroxy-3-oxo-2,3-dihydro-indole-2-carboxylic acid ethyl ester 
• 617-36-7 Ethyl oxamate 
• 4755-77-5 Ethyl oxalyl chloride 

Downstream Products

• 64-17-5 ethanol 
• 144-62-7 oxalic acid 
• 118-92-3 anthranilic acid 
• 72426-19-8 2-[(5-amino-[1,3,4]thiadiazole-2-sulfonylaminooxalyl)-amino]-benzoic acid 
• 51679-96-0 N₁-(2-carboxyphenyl)-N₂-(2-hydroxyethyl)oxalamide 
• 5651-01-4 2-(oxalamino)benzoic acid 
• 76508-91-3 2-{[(1S,2S)-2-Hydroxy-1-hydroxymethyl-2-(4-nitro-phenyl)-ethylaminooxalyl]-amino}-benzoic acid 
• 76508-91-3 2-{[(1R,2R)-2-Hydroxy-1-hydroxymethyl-2-(4-nitro-phenyl)-ethylaminooxalyl]-amino}-benzoic acid 
• 67472-16-6 2-(Hydroxyaminooxalyl-amino)-benzoic acid 
• 72117-60-3 2-Carboxyoxanilic acid hydrazide 

Relevant articles and documents

Synthesis and structure of a 1-D copper(II) coordination polymer bridged both by oxamido and carboxylate: In vitro anticancer activity and reactivity toward DNA and protein BSA

A 1-D copper(II) coordination polymer formulated as {[Cu2(bdpox)(dabt)](NO3)?H2O}n, where H3bdpox and dabt denote N-benzoate-N'-[3-(diethylamino)propyl]oxamide and 2,2'-diamino-4,4'-bithiazole, respec

Guanidinum chloride as dehydrocyclization agent in the synthesis of 2-fuctionalized (4H)-3,1-benzoxazine-4-ones

A facile and expedient route for the synthesis of 2-ethoxy- and 2-(ethylcarboxylate)-(4H)-3,1-benzoxazine-4-ones is described using guanidinium chloride as a safe and convenient dehydrocyclization agent. High yields of the products obtain under mild react

Reactions of ethyl oxamate and dialkyl oxalates with anthranilic acid derivatives

Ethyl oxamate reacted with anthranilic acid derivatives at the amide or the ester group leading to the formation of respective esters or amides. A simple method was developed for preparation of alkyl 3-amino-4-oxo-3,4- dihydroquinazoline-2-carboxylates. Nauka/Interperiodica 2007.