149340-93-2

Basic information

• Product Name: N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea
• Synonyms: N-[2-(4-nitrophenyl)ethyl]-N'-propyl-Urea;Urea, N-[2-(4-nitrophenyl)ethyl]-N'-propyl-;1-(4-Nitrophenethyl)-3-propylurea
• CAS NO: 149340-93-2
• Molecular Formula: C₁₂H₁₇N₃O₃
• Molecular Weight: 251.28
• Mol File: 149340-93-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 489.0±28.0 °C(Predicted)
• Appearance: /
• Density: 1.169
• Storage Temp.: 2-8°C
• PKA: 14.11±0.46(Predicted)
• CAS DataBase Reference: N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea(149340-93-2)
• EPA Substance Registry System: N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea(149340-93-2)

Safety Data

• Hazardous Substances Data: 149340-93-2(Hazardous Substances Data)

Usage

General Description

N-[2-(4-Nitrophenyl)ethyl]-N'-propylurea is a synthetic, organic compound that consists of a urea backbone chemically bonded to a nitrophenyl group and a propyl chain. The presence of the nitrophenyl and ethyl groups suggests it may have unique optical properties, but its specific applications and characteristics are not widely reported in scientific literature. Like other urea compounds, it may have industrial uses such as solvents, detergents, or as a chemical intermediate for pharmaceuticals and other chemicals. However, its nitrophenyl group may also lead to explosive or reactive properties, requiring careful handling. As always, further study and full understanding of this chemical structure are needed to determine its potential applications.

Upstream product

• 110-78-1 Propyl isocyanate 
• 29968-78-3 2-(4-nitrophenyl)ethylamine monohydrochloride 
• 24954-67-4 2-(p-nitrophenyl)ethylamine 

Downstream Products

• 149741-48-0 1-cyanoacetyl-1-[2-(4-nitrophenyl)ethyl]-1'-propylurea 
• 149340-94-3 1-(cyanoacetyl)-3-(4-nitrophenethyl)-1-propylurea 
• 149341-00-4 6-amino-1-<4-<(benzyloxycarbonyl)amino>phenethyl>-5-<(cyclopentanecarbonyl)amino>-3-propyluracil 
• 149340-98-7 6-amino-1-<4-<(benzyloxycarbonyl)amino>phenethyl>-5-nitroso-3-propyluracil 
• 149741-55-9 6-amino-1-(4-aminophenethyl)-5-<(3-noradamantylcarbonyl)amino>-3-propyluracil 
• 149741-42-4 3-(4-aminophenethyl)-8-(3-noradamantyl)-1-propylxanthine 
• 149340-99-8 5,6-diamino-1-(4-benzyloxycarbonylaminophenethyl)-3-propyluracil 
• 149744-75-2 N-{4-[2-(8-Cyclopentyl-2,6-dioxo-1-propyl-1,2,6,7-tetrahydro-purin-3-yl)-ethyl]-phenyl}-acetamide 
• 149340-97-6 6-amino-1-<4-<(benzyloxycarbonyl)amino>phenethyl>-3-propyluracil 
• 116370-30-0 [125I]-BW-A 844U 
• 149340-95-4 6-amino-1-(4-nitrophenethyl)-3-propyluracil 
• 149340-96-5 6-amino-1-(4-aminophenethyl)-3-propyluracil 

Relevant articles and documents

A1 ADENOSINE RECEPTOR ANTAGONISTS

Compounds of the general formula (I) are described wherein A is a 5- or 6-membered aromatic or heteroaromatic ring. Compositions comprising such compounds and methods of use thereof are also described.

Adenosine A1 antagonists. 3. Structure-activity relationships on amelioration against scopolamine- or N6-((R)-phenylisopropyl)adenosine-induced cognitive disturbance.

The effects of a variety of adenosine A1 and A2 antagonists on N6-((R)-phenylisopropyl)adenosine (R-PIA)- and scopolamine-induced amnesias were investigated in rodents in order to clarify the role of adenosine receptors in learning and memory. Some of the