212189-50-9

Basic information

• Product Name: METHYL 2-(4-NITROPHENOXY)BENZENECARBOXYLATE
• Synonyms: METHYL 2-(4-NITROPHENOXY)BENZENECARBOXYLATE
• CAS NO: 212189-50-9
• Molecular Formula: C₁₄H₁₁NO₅
• Molecular Weight: 273.24
• Mol File: 212189-50-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 74-77°C
• Appearance: /
• CAS DataBase Reference: METHYL 2-(4-NITROPHENOXY)BENZENECARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 2-(4-NITROPHENOXY)BENZENECARBOXYLATE(212189-50-9)
• EPA Substance Registry System: METHYL 2-(4-NITROPHENOXY)BENZENECARBOXYLATE(212189-50-9)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 212189-50-9(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 6082-87-7 o-carboxyphenyl p-nitrophenyl ether 
• 2444-29-3 1-methyl-2-(4-nitrophenoxy)benzene 
• 100-02-7 4-nitro-phenol 
• 118-91-2 ortho-chlorobenzoic acid 
• 350-46-9 4-Fluoronitrobenzene 
• 119-36-8 methyl salicylate 

Downstream Products

• 212189-58-7 methyl2-(4-aminophenoxy)benzoate 
• 1416568-24-5 methyl 2-[4-[[(4-quinolinylmethyl)amino]sulfonyl]phenoxy]-benzoate 
• 1416569-29-3 methyl 2-[4-(chlorosulfonyl)phenoxy]benzoate 
• 1596360-80-3 9H-fluoren-9-ylmethyl N-[(5S)-5-[[6-[[3-[4-(2-carbamoylphenoxy)phenyl]-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carbonyl]amino]-5-cyano-pentyl]carbamate 
• 1596360-37-0 N-[(1S)-5-amino-1-cyano-pentyl]-6-[[3-[4-(2-carbamoylphenoxy)phenyl]-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxamide 
• 1596360-93-8 methyl 2-{4-[(tert-butoxy)carbonylamino]phenoxy}benzoate 
• 1596360-94-9 2-{4-[(tert-butoxy)carbonylamino]phenoxy}benzoic acid 
• 1596360-95-0 2-{4-[(tert-butoxy)carbonylamino]phenoxy}benzamide 
• 1596360-96-1 ethyl2-{[4-(2-carbamoylphenoxy)phenyl]amino}acetate 
• 1596360-07-4 2-[4-(2,4-dioxo-1,3-diazolidinyl)phenoxy]benzamide 
• 307308-74-3 C₁₃H₁₂N₂O₂ 
• 1596360-57-4 methyl 6-[[3-[4-(2-carbamoylphenoxy)phenyl]-2,5-dioxo-imidazolidin-1-yl]methyl]-7-methyl-pyrrolo[2,3-d]pyrimidine-2-carboxylate 
• 6082-87-7 o-carboxyphenyl p-nitrophenyl ether 

Relevant articles and documents

A photoredox-neutral Smiles rearrangement of 2-aryloxybenzoic acids

We report on the use of visible light photoredox catalysis for the radical Smiles rearrangement of 2-aryloxybenzoic acids to obtain aryl salicylates. The method is free of noble metals and operationally simple and the reaction can be run under mild batch or flow conditions. Being a redox neutral process, no stoichiometric oxidants or reductants are needed.

HETEROCYCLIC COMPOUNDS FOR TREATING HELMINTH INFECTIONS

Disclosed are compounds of Formula 1, N-oxides, and salts thereof, wherein L is (CR13aR13b)t,, CR14=CR14, C≡C, CR15aR15bX, XCR15aR15b, CO, O, S(O)p, NR