Methyl 2-(4-nitrophenoxy)benzoate

Base Information

• Chemical Name: Methyl 2-(4-nitrophenoxy)benzoate
• CAS No.: 212189-50-9
• Molecular Formula: C14H11NO5
• Molecular Weight: 273.245
• Hs Code.: 2918990090
• DSSTox Substance ID: DTXSID80377166
• Wikidata: Q82166265
• Mol file: 212189-50-9.mol

Synonyms:methyl 2-(4-nitrophenoxy)benzoate;212189-50-9;methyl 2-(4-nitrophenoxy)benzenecarboxylate;Benzoic acid, 2-(4-nitrophenoxy)-, methyl ester;SCHEMBL10922122;DTXSID80377166;methyl2-(4-nitrophenoxy)benzoate;PVVIPSBIFWHOIX-UHFFFAOYSA-N;methyl 2-(4'-nitrophenoxy)benzoate;AB7560;MFCD04117807;AKOS001337572;CS-0301982;3X-0705;J-521849;Z52589691

Chemical Property of Methyl 2-(4-nitrophenoxy)benzoate

Chemical Property:

• Melting Point: 74-77°C
• PSA: 81.35000
• LogP: 3.69690
• XLogP3: 3.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 273.06372245
• Heavy Atom Count: 20
• Complexity: 346

Purity/Quality:

98%min ^*data from raw suppliers

Methyl 2-(4-nitrophenoxy)benzenecarboxylate >95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC(=O)C1=CC=CC=C1OC2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of Methyl 2-(4-nitrophenoxy)benzoate

There total 6 articles about Methyl 2-(4-nitrophenoxy)benzoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 78.0%

4-Fluoronitrobenzene (350-46-9,178603-76-4) + methyl salicylate (119-36-8,8024-54-2) → methyl2-(4-nitrophenoxy)benzoate (212189-50-9)

Guidance literature:

With potassium carbonate; In acetonitrile; at 80 ℃; for 24h;

DOI:10.1016/j.bmc.2014.02.002

Reference yield:

2-hydroxy methylbenzoate + 4-Fluoronitrobenzene (350-46-9,178603-76-4) → methyl2-(4-nitrophenoxy)benzoate (212189-50-9)

Guidance literature:

With caesium carbonate; In acetone; at 20 ℃; for 48h;

Reference yield:

methanol (67-56-1) + o-carboxyphenyl p-nitrophenyl ether (6082-87-7) → methyl2-(4-nitrophenoxy)benzoate (212189-50-9)

Guidance literature:

With hydrogenchloride;

DOI:10.1039/jr9510000757

upstream raw materials:

methanol

o-carboxyphenyl p-nitrophenyl ether

1-methyl-2-(4-nitrophenoxy)benzene

4-nitro-phenol

Downstream raw materials:

methyl 2-[4-[[(4-quinolinylmethyl)amino]sulfonyl]phenoxy]-benzoate

methyl 2-[4-(chlorosulfonyl)phenoxy]benzoate

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

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

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