6855-54-5

Basic information

• Product Name: 3-benzyloxy-2-nitrophenyl-acetic acid
• Synonyms: 3-benzyloxy-2-nitrophenyl-acetic acid
• CAS NO: 6855-54-5
• Molecular Weight: 287.272
• Mol File: 6855-54-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-benzyloxy-2-nitrophenyl-acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-benzyloxy-2-nitrophenyl-acetic acid(6855-54-5)
• EPA Substance Registry System: 3-benzyloxy-2-nitrophenyl-acetic acid(6855-54-5)

Safety Data

• Hazardous Substances Data: 6855-54-5(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 110655-06-6 (3-benzyloxy-2-nitro-phenyl)-pyruvic acid 
• 61535-21-5 1-(benzyloxy)-3-methyl-2-nitrobenzene 
• 4920-77-8 3-methyl-2-nitrophenol 
• 96564-49-7 C₁₈H₁₆NO₆^(1-)*K⁽¹⁺⁾ 
• 95-92-1 oxalic acid diethyl ester 

Downstream Products

• 74864-81-6 7-benzyloxy-2-indolinone 
• 110655-08-8 [7-Benzyloxy-2-oxo-1,2-dihydro-indol-(3E)-ylidene]-hydroxy-acetic acid 
• 110655-09-9 benzyl (7-benzyloxy-2-oxindolin-3-yl)glyoxylate 
• 1206201-48-0 methyl 2-(3-(benzyloxy)-2-nitrophenyl)ethanoate 
• 110655-09-9 C₂₄H₁₉NO₅ 
• 191730-78-6 7-benzyloxyindoline 

Relevant articles and documents

Synthesis of tetrahydropyrroloiminoquinone alkaloids based on electrochemically generated hypervalent iodine oxidative cyclization

[Chemical equation presented] An approach to the synthesis of the tetrahydropyrroloiminoquinone alkaloids has been developed and applied to the preparation of N-1-βD-ribofuranosyltetrahydropyrroloiminoquinones. The strategy utilizes oxidative cyclization

5-HT4 receptor agonists

Compounds of formula (I) and pharmaceutically acceptable salts thereof are selective agonists for 5-HT4 receptors. STR1 wherein Ak is a C3 -C6 alkyl group, and R is a C2 -C6 alkyl group, a C3 -C6 alkenyl group, a C3 -C6 alkynyl group, a C3 -C7 cycloalkyl group or a C3 -C6 cycloalkylmethyl group.