1-Nitro-2-[3-(2-nitrophenoxy)propoxy]benzene

Base Information

• Chemical Name: 1-Nitro-2-[3-(2-nitrophenoxy)propoxy]benzene
• CAS No.: 14467-63-1
• Molecular Formula: C₁₅H₁₄N₂O₆
• Molecular Weight: 318.286
• European Community (EC) Number: 653-251-9

Synonyms:1-nitro-2-[3-(2-nitrophenoxy)propoxy]benzene;14467-63-1;SCHEMBL9642715;QFTHUUKTCANIBG-UHFFFAOYSA-N;AKOS024334070;SR-01000206948;SR-01000206948-1;1,1'-[propane-1,3-diylbis(oxy)]bis(2-nitrobenzene);Benzene, 1,1'-[1,3-propanediylbis(oxy)]bis[2-nitro-

Chemical Property of 1-Nitro-2-[3-(2-nitrophenoxy)propoxy]benzene

Chemical Property:

• XLogP3: 3.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 6
• Exact Mass: 318.08518617
• Heavy Atom Count: 23
• Complexity: 358

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)[N+](=O)[O-])OCCCOC2=CC=CC=C2[N+](=O)[O-]

Technology Process of 1-Nitro-2-[3-(2-nitrophenoxy)propoxy]benzene

There total 6 articles about 1-Nitro-2-[3-(2-nitrophenoxy)propoxy]benzene 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: 95.0%

1,3-dibromo-propane (109-64-8) + 2-hydroxynitrobenzene (88-75-5,78813-12-4) → 1,5-bis-(2-nitrophenyl)-1,5-dioxapentane (14467-63-1)

Guidance literature:

With 18-crown-6 ether; sodium carbonate; In N,N-dimethyl-formamide; at 140 ℃; for 5h;

Reference yield: 90.0%

1.3-chlorobromopropane (109-70-6) + 2-hydroxynitrobenzene (88-75-5,78813-12-4) → 1,5-bis-(2-nitrophenyl)-1,5-dioxapentane (14467-63-1)

Guidance literature:

2-hydroxynitrobenzene; With potassium carbonate; In N,N-dimethyl-formamide;

1.3-chlorobromopropane; With potassium iodide; In N,N-dimethyl-formamide; Heating;

In N,N-dimethyl-formamide; at 110 ℃; for 2h;

DOI:10.1002/ejoc.202100948

Reference yield: 72.0%

sodium o-nitrophenate (824-39-5) + 1,3-dibromo-propane (109-64-8) → 1,5-bis-(2-nitrophenyl)-1,5-dioxapentane (14467-63-1)

Guidance literature:

In N,N-dimethyl-formamide; for 2h; Heating;

upstream raw materials:

potassium 4-nitrophenolate

1,3-dibromo-propane

sodium o-nitrophenate

2-hydroxynitrobenzene

Downstream raw materials:

1,3-bis(o-aminophenoxy)propane-N,N,N',N'-tetraacetic acid

1,3-bis<2-amino>phenoxy>propane

2-[[2-(3-{2-[Bis-(2-hydroxy-ethyl)-amino]-phenoxy}-propoxy)-phenyl]-(2-hydroxy-ethyl)-amino]-ethanol

16-(Toluene-4-sulfonyl)-2,6-dioxa-13,16,19-triaza-tricyclo[18.4.0.0^7,12]tetracosa-1⁽²⁴⁾,7⁽¹²⁾,8,10,20,22-hexaene

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