475215-88-4

Basic information

• Product Name: Methyl 4-amino-3-(benzyloxy)benzoate
• Synonyms: Methyl 4-amino-3-(benzyloxy)benzoate;methyl 4-amino-3-phenylmethoxybenzoate;Methyl 4-amino-3-(benzyloxy)benzenecarboxylate（WS204176）
• CAS NO: 475215-88-4
• Molecular Formula: C₁₅H₁₅NO₃
• Molecular Weight: 257.29
• Mol File: 475215-88-4.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl 4-amino-3-(benzyloxy)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 4-amino-3-(benzyloxy)benzoate(475215-88-4)
• EPA Substance Registry System: Methyl 4-amino-3-(benzyloxy)benzoate(475215-88-4)

Safety Data

• Hazardous Substances Data: 475215-88-4(Hazardous Substances Data)

Usage

General Description

Methyl 4-amino-3-(benzyloxy)benzoate is an organic compound that belongs to the class of benzoic acid derivatives. It is composed of a methyl ester group attached to a benzoic acid molecule, with an amino group at the 4-position and a benzyloxy group at the 3-position of the benzene ring. This chemical has potential applications in the pharmaceutical industry as a building block for the synthesis of various bioactive compounds. It may also be used as an intermediate in the production of dyes, pigments, and other organic substances. Additionally, it is important to handle this compound with care as it may present hazards if not used properly in a controlled environment.

Upstream product

• 209528-69-8 methyl 3-(benzyloxy)-4-nitrobenzoate 
• 941715-63-5 C₂₀H₂₃NO₅ 
• 100-39-0 benzyl bromide 
• 941715-62-4 methyl 4-(t-butoxycarbonylamino)-3-hydroxybenzoate 
• 63435-16-5 3-hydroxy-4-aminobenzoic acid methyl ester 
• 619-14-7 3-hydroxy-4-nitro-benzoic acid 

Downstream Products

• 881909-58-6 methyl 4-amino-3-benzyloxy-5-bromobenzoate 
• 911369-89-6 methyl 3-benzyloxy-5-bromo-4-[(trifluoroacetyl)amino]benzoate 
• 941715-72-6 methyl 4-acetamido-3-(benzyloxy)benzoate 
• 881909-62-2 methyl 3-ethyl-7-[(phenylmethyl)oxy]-1H-indole-5-carboxylate 
• 881909-60-0 methyl 3-bromo-4-[(2E,Z)-2-buten-1-yl(trifluoroacetyl)amino]-5-[(phenylmethyl)oxy]benzoate 
• 1058114-89-8 4-acetamido-3-(benzyloxy)benzoic acid 
• 1058114-27-4 C₁₆H₁₄ClNO₃ 
• 941715-73-7 C₂₄H₂₂N₂O₆ 
• 941715-74-8 C₃₁H₂₇FN₂O₆ 
• 1058114-95-6 C₃₀H₂₅FN₂O₆ 
• 941715-75-9 C₃₈H₃₂FN₃O₈ 
• 475215-89-5 3-benzyloxy-4-chlorosulfonyl-benzoic acid methyl ester 
• 1069130-70-6 methyl 3-benzyloxy-4-(4-methoxyphenylamino)benzoate 
• 1379520-51-0 methyl 3-(benzyloxy)-4-(3-benzyloxy-4-nitrobenzamido)-benzoate 

Relevant articles and documents

NEW CLASS OF DNA GYRASE AND/OR TOPOISOMERASE IV INHIBITORS WITH ACTIVITY AGAINST GRAM-POSITIVE AND GRAM-NEGATIVE BACTERIA

The present invention relates to compounds having a structure of general formula (I), processes for their preparation, pharmaceutical compositions containing them as the active ingredient, to their use as medicaments and to their use in the manufacture of medicaments for use in the treatment of bacterial infections in humans and warm-blooded animals.

Transition metals in organic synthesis. Part 101: Convergent total synthesis of 1,6-dioxygenated carbazole alkaloids

Using a palladium(II)-catalysed oxidative cyclisation as key step, we describe a highly efficient total synthesis of a series of naturally occurring 1,6-dioxygenated carbazole alkaloids: clausenine, 6-methoxymurrayanine, clausenol, clausine G, clausine I, clausine Z and methyl 1,6-dihydroxy-9H- carbazole-3-carboxylate.

Transition metals in organic synthesis, Part 85.1 A general approach to 1,6-dioxygenated carbazole alkaloids - first total synthesis of clausine G, clausine I, and clausine Z

Using the palladium-catalyzed construction of the carbazole framework, a highly efficient route to 1,6-dioxygenated carbazole alkaloids has been developed and applied to the total synthesis of clausenine, 6- methoxymurrayanine, clausenol, clausine G, clausine I, and clausine Z. The three latter natural products have been synthesized for the first time. Thieme Stuttgart.