104356-42-5

Basic information

• Product Name: 5-(benzyloxy)-2-((ethoxycarbonyl)amino)benzoic acid
• Synonyms: 5-(benzyloxy)-2-((ethoxycarbonyl)amino)benzoic acid
• CAS NO: 104356-42-5
• Molecular Weight: 315.326
• Mol File: 104356-42-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-(benzyloxy)-2-((ethoxycarbonyl)amino)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(benzyloxy)-2-((ethoxycarbonyl)amino)benzoic acid(104356-42-5)
• EPA Substance Registry System: 5-(benzyloxy)-2-((ethoxycarbonyl)amino)benzoic acid(104356-42-5)

Safety Data

• Hazardous Substances Data: 104356-42-5(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 394-31-0 2-amino-5-hydroxybenzoic acid 
• 622829-44-1 benzyl 5-(benzyloxy)-2-((ethoxycarbonyl)amino)benzoate 

Downstream Products

• 929859-22-3 7-(benzyloxy)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one 
• 85654-22-4 2-hydroxy-7,8-dihydro-6H,11H-pyrrolo[2,1-b]quinazolin-11-one 
• 1539278-94-8 10-(benzyloxy)-13-methyl-13,13a-dihydro-5H-isoquinolino[1,2-b]quinazolin-8(6H)-one 
• 1615687-56-3 3-(benzyloxy)-14-methyl-7,8,13b,14-tetrahydroindolo[20,30:3,4]pyrido[2,1-b]quinazolin-5(13H)-one 
• 1615687-69-8 14-methyl-5,7,8,13,13b,14-hexahydroindolo[2',3':3,4]pyrido[2,1-b]quinazolin-3-yl(3-methoxyphenyl)carbamate 
• 1615687-68-7 14-methyl-5,7,8,13,13b,14-hexahydroindolo[2',3':3,4]pyrido[2,1-b]quinazolin-3-yl(4-isopropylphenyl)carbamate 
• 1615687-67-6 14-methyl-5,7,8,13,13b,14-hexahydroindolo[2',3':3,4]pyrido[2,1-b]quinazolin-3-ylbenzylcarbamate 
• 1615687-63-2 14-methyl-5-oxo-5,7,8,13,13b,14-hexahydroindolo[2',3':3,4]pyrido[2,1-b]quinazolin-3-yl(3-methoxyphenyl)carbamate 
• 1615687-62-1 14-methyl-5-oxo-5,7,8,13,13b,14-hexahydroindolo[2',3':3,4]pyrido[2,1-b]quinazolin-3-yl(4-isopropylphenyl)carbamate 
• 1615687-61-0 14-methyl-5,7,8,13,13b,14-hexahydroindolo[2',3':3,4]pyrido[2,1-b]quinazolin-3-ylbenzylcarbamate 
• 104356-44-7 ethyl [2-[[2-[4[ 2-(4-fluorophenyl)-1,3-dioxolan-2-yl]-1-piperidinyl]ethyl]aminocarbonyl]-4-(phenylmethoxy)phenyl]carbamate 

Relevant articles and documents

Synthesis, biological evaluation, and computational studies of Tri- and tetracyclic nitrogen-bridgehead compounds as potent dual-acting AChE inhibitors and h H3 receptor antagonists

Combination of AChE inhibiting and histamine H3 receptor antagonizing properties in a single molecule might show synergistic effects to improve cognitive deficits in Alzheimer's disease, since both pharmacological actions are able to enhance ch

Approach to the synthesis of (+)-ifforestine. Model studies directed at the tetracyclic framework

In order to design an effective asymmetric synthesis of (+)-ifforestine, model approaches to the construction of the tetracyclic ring system have been investigated. These studies have identified two key synthons, a functionalized isatoic anhydride and a p