3722-79-0

Basic information

• Product Name: 1-nitro-4-[3-(4-nitrophenoxy)propoxy]benzene
• CAS NO: 3722-79-0
• Molecular Formula: C₁₅H₁₄N₂O₆
• Molecular Weight: 318.286
• Mol File: 3722-79-0.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 1-nitro-4-[3-(4-nitrophenoxy)propoxy]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-nitro-4-[3-(4-nitrophenoxy)propoxy]benzene(3722-79-0)
• EPA Substance Registry System: 1-nitro-4-[3-(4-nitrophenoxy)propoxy]benzene(3722-79-0)

Safety Data

• Hazardous Substances Data: 3722-79-0(Hazardous Substances Data)

Usage

Description

1-nitro-4-[3-(4-nitrophenoxy)propoxy]benzene is a chemical compound with the molecular formula C18H15N3O7. It is a nitrobenzene derivative with a long chain of oxypropyl groups linked to the benzene ring. With multiple nitro and oxypropyl groups attached, this compound is highly reactive and potentially explosive.

Uses

Used in Organic Compounds Industry:
1-nitro-4-[3-(4-nitrophenoxy)propoxy]benzene is used as a raw material for the synthesis of various organic compounds due to its reactive nature and the presence of multiple functional groups.
Used in Dyes Industry:
1-nitro-4-[3-(4-nitrophenoxy)propoxy]benzene is used as an intermediate in the production of dyes, where its reactive groups can be utilized to create a wide range of colorants.
Used in Pharmaceuticals Industry:
1-nitro-4-[3-(4-nitrophenoxy)propoxy]benzene is used as a building block in the development of pharmaceuticals, where its unique structure can be employed to create novel drug candidates.
Safety Precautions:
Due to its toxicity and potential explosiveness, 1-nitro-4-[3-(4-nitrophenoxy)propoxy]benzene should be handled with extreme caution and proper safety measures should be implemented during its use and storage.

Upstream product

• 100-02-7 4-nitro-phenol 
• 109-64-8 1,3-dibromo-propane 
• 1124-31-8 potassium 4-nitrophenolate 
• 13094-50-3 1-(3-bromopropoxy)-4-nitrobenzene 
• 100-00-5 4-chlorobenzonitrile 
• 504-63-2 trimethyleneglycol 
• 824-78-2 4-nitrophenol sodium salt 

Downstream Products

• 52980-20-8 1,3-bis(4-aminophenoxy)propane 
• 128911-65-9 1,3-bis-(4-isocyanato-phenoxy)-propane 
• 7476-06-4 1,3-bis(4-cyanophenoxy)propane 
• 104-32-5 propamidine 
• 133024-74-5 1,3-Bis[p-[(2,4-dioxo-5-thiazolidinyl)methyl]phenoxy]propane 
• 146885-98-5 1,3-di(thiourea-4-phenoxy)propane 

Relevant articles and documents

Synthesis and crystal structure of 1,3-bis(p-nitrophenoxy)propane

The title compound 1,3-bis(p-nitrophenoxy)propane was synthesized by nucleophilic substitution of p-nitrophenol and 1,3-dibromopropane. Single crystal X-ray diffraction analysis reveals that the molecule in the solid state packs in the monoclinic P2/n spa

Green synthesis of symmetric aryl ether dinitro compounds in deep eutectic solvents

A series of symmetric aryl ether dinitro compounds were synthesized by 4Urea/ZnCl2 as green solvent and catalyst, and halogenated aromatic hydrocarbon derivatives and dihydroxy compounds as raw materials. This method has the advantages of easy operation, simple recrystallization, environmental friendliness and biodegradability. The structures of the products were subjected to 1H NMR, and the reaction conditions, reaction mechanism and greening advantages of deep eutectic solvents were discussed at the end of the experiments. We learned from the results of the experiments that both the aliphatic dihydroxy compounds and the aromatic dihydroxy compounds could proceed effectively in Ullmann reaction, and the desired products could be obtained in acceptable yields. When using this methodology, symmetric aryl ether dinitro compounds could be synthesized simply at 80oC in 2 h with high yields (66%~94%). Meanwhile, the DES, called deep eutectic solvent which is composed of 4Urea/ZnCl2, could be recycled at least five times without an obvious decraese in the catalytic activity.

Synthesis and characterization of new optically active poly(amide-imide)s based on n-trimellitimido-l-amino acid and trimethylene units

Six new optically active poly(amide-imide)s (8a-f) were synthesized through the direct polycondensation reaction of 1,3-bis(4-aminophenoxy) propane (4) with six different derivatives of N-trimellitimido-L-amino acid (7a-f) in a medium consisting of N-meth