5690-41-5

Basic information

• Product Name: (4Z)-2-(2-bromophenyl)-4-(4-ethoxybenzylidene)-1,3-oxazol-5(4H)-one
• Synonyms: 5(4H)-oxazolone, 2-(2-bromophenyl)-4-[(4-ethoxyphenyl)methylene]-, (4Z)-
• CAS NO: 5690-41-5
• Molecular Formula: C₂₃H₁₆O
• Molecular Weight: 372.2127
• Mol File: 5690-41-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 488.9°C at 760 mmHg
• Flash Point: 249.5°C
• Density: 1.41g/cm³
• Vapor Pressure: 1.05E-09mmHg at 25°C
• Refractive Index: 1.614
• CAS DataBase Reference: (4Z)-2-(2-bromophenyl)-4-(4-ethoxybenzylidene)-1,3-oxazol-5(4H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (4Z)-2-(2-bromophenyl)-4-(4-ethoxybenzylidene)-1,3-oxazol-5(4H)-one(5690-41-5)
• EPA Substance Registry System: (4Z)-2-(2-bromophenyl)-4-(4-ethoxybenzylidene)-1,3-oxazol-5(4H)-one(5690-41-5)

Safety Data

• Hazardous Substances Data: 5690-41-5(Hazardous Substances Data)

Usage

Description

(4Z)-2-(2-bromophenyl)-4-(4-ethoxybenzylidene)-1,3-oxazol-5(4H)-one is a complex organic compound featuring an oxazolone ring system and a bromophenyl group. The inclusion of an ethoxybenzylidene group indicates potential pharmaceutical applications, as similar structures have demonstrated biological activity. However, the specific properties and uses of this chemical require further research and testing to be fully understood.

Uses

Used in Pharmaceutical Industry:
(4Z)-2-(2-bromophenyl)-4-(4-ethoxybenzylidene)-1,3-oxazol-5(4H)-one is used as a potential pharmaceutical agent due to its complex molecular structure and the presence of functional groups that may exhibit biological activity. Further research is necessary to explore its specific applications and therapeutic potential.

Upstream product

• 56-23-5 tetrachloromethane 
• 90-15-3 α-naphthol 
• 2051-90-3 Dichlorodiphenylmethane 
• 861331-55-7 1-bromo-4-(α-chloro-benzhydryl)-naphthalene 
• 98-95-3 nitrobenzene 
• 859941-87-0 1-hydroxy-4-(α-hydroxy-benzhydryl)-[2]naphthoic acid 
• 86-48-6 1-hydroxy-2-naphthoic acid 
• 76-93-7 Benzilic acid 
• 861074-09-1 (3-carboxy-4-hydroxy-[1]naphthyl)-diphenyl-acetic acid 
• 62345-25-9 4-methoxynaphthyldiphenylmethanol 
• 80094-07-1 dimethyl <4-(diphenylmethylene)-1,4-dihydro-1-hydroxynaphthyl>phosphonate 
• 51431-91-5 [4-(α-chloro-benzhydryl)-[1]naphthyl]-methyl ether 
• 432492-40-5 4-Oxy-1-(α-oxy-benzhydryl)-naphthalin 

Downstream Products

• 138690-93-4 1,1'-di<-4-(diphenylmethylene)-1,4-dihydronaphthyl>-dithietanes 
• 138690-92-3 diphenyl-1-S-<4-(diphenylmethylene)-1,4-dihydro-1-hydroxynaphthyl>-dithiophosphinic acid ester 
• 85523-56-4 2,3-dihydro-2,2,3-tribromo-1,4-naphthofuchsone 
• 85523-57-5 2,3-dibromo-4-(diphenylmethylene)-1-(4H)naphthalenone 
• 62345-29-3 ethyl-(4-benzhydryl-[1]naphthyl)-ether 
• 62345-27-1 (4-Ethoxynaphthyl)-diphenylmethanol 
• 62345-28-2 Ethyl-(4-ethoxynaphthyl)-diphenylmethylether 
• 95684-06-3 4-(diphenylmethylene)-2-chloro-1(4H)-naphthalenone 
• 104601-29-8 11-phenylbenzofluorene 
• 6274-86-8 4-benzhydrylnaphthalen-1-ol 
• 432492-40-5 4-Oxy-1-(α-oxy-benzhydryl)-naphthalin 
• 62345-26-0 Methyl-(4-methoxynaphthyl)-diphenylmethylether 
• 62345-25-9 4-methoxynaphthyldiphenylmethanol 
• 135763-08-5 (4-Benzhydrylidene-1-hydroxy-1,4-dihydro-naphthalen-1-yl)-(triphenyl-λ⁵-phosphanylidene)-acetonitrile 

Relevant articles and documents

ORGANOPHOSPHORUS COMPOUNDS, XXXII THE REACTION OF ALKYL PHOSPHITES WITH 1-(DIPHENYLMETHYLENE)-2(1H)- AND 4-(DIPHENYLMETHYLENE)-1(4H)-NAPHTHALENONES

1-(Diphenylmethylene)-2(1H)-naphthalenone (1) reacts with trialkyl phosphites to give the corresponding 1,2-dihydro-2-alkoxy-1,1-diphenylnaphth-oxaphosphole-2-oxides (3a-c).The latter compounds are equally obtained by the reaction of dialkyl phosphites with 1.A mechanism for this reaction is presented which accounts for the experimental results.On the other hand, 4-(diphenylmethylene)-1(4H)-naphthalenone (2) reacts only with dialkyl phosphites to give dialkyl-phosphonates (9a-c).Structural assignments are based on analytical, chemical and spectroscopic evidence.