2734-78-3

Basic information

• Product Name: 1-(benzyloxy)-2,4-dinitrobenzene
• CAS NO: 2734-78-3
• Molecular Formula: C₁₃H₁₀N₂O₅
• Molecular Weight: 274.2289
• Mol File: 2734-78-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 454.6°C at 760 mmHg
• Flash Point: 208.7°C
• Density: 1.386g/cm³
• Vapor Pressure: 5.07E-08mmHg at 25°C
• Refractive Index: 1.631
• CAS DataBase Reference: 1-(benzyloxy)-2,4-dinitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(benzyloxy)-2,4-dinitrobenzene(2734-78-3)
• EPA Substance Registry System: 1-(benzyloxy)-2,4-dinitrobenzene(2734-78-3)

Safety Data

• Hazardous Substances Data: 2734-78-3(Hazardous Substances Data)

Usage

General Description

1-(benzyloxy)-2,4-dinitrobenzene is a chemical compound with the molecular formula C14H11N3O5. It is a yellow crystalline solid that is commonly used in organic synthesis and as a reagent in chemistry. 1-(benzyloxy)-2,4-dinitrobenzene is often used in the preparation of other organic molecules and is known for its ability to undergo various chemical reactions, such as nucleophilic aromatic substitution and reduction reactions. It is important to handle this chemical with caution, as it is toxic and may cause skin and eye irritation upon contact. Additionally, its toxic effects on the environment should be taken into consideration when using and disposing of this compound.

Upstream product

• 51-28-5 2,4-Dinitrophenol 
• 1760-29-8 1-Benzyl-2-guanyl-1-nitroso-hydrazin 
• 100-39-0 benzyl bromide 
• 46121-22-6 benzylamino-guanidine 
• 2831-60-9 2-(2,4-dinitrophenoxy)ethanol 
• 2486-07-9 2,4-dinitrophenyl phenyl ether 
• 620-05-3 iodomethylbenzene 
• 70-34-8 2,4-Dinitrofluorobenzene 
• 100-51-6 benzyl alcohol 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 100-44-7 benzyl chloride 
• 10242-18-9 Allyl 2,4-dinitrophenyl ether 

Downstream Products

• 88964-90-3 2-amino-4-nitrophenyl benzyl ether 
• 1621090-63-8 diethyl 4-(benzyloxy)-1,3-phenylenedicarbamate 
• 1621090-69-4 6-(benzyloxy)quinazoline-7-amine 
• 1621090-18-3 1-(6-(benzyloxy)quinazolin-7-yl)-3-p-tolylurea 
• 1621090-19-4 1-(6-(benzyloxy)quinazolin-7-yl)-3-(naphthalen-1-yl)urea 
• 1621090-20-7 1-(6-(benzyloxy)quinazolin-7-yl)-3-(3,4-dichlorophenyl)urea 
• 1621090-21-8 1-(6-(benzyloxy)quinazolin-7-yl)-3-(3-fluorophenyl)urea 
• 51-28-5 2,4-Dinitrophenol 
• 99974-28-4 1-furfuryloxy-2,4-dinitro-benzene 
• 4279-47-4 (2,4-dinitro-phenyl)-(4-nitro-benzyl)-ether 
• 99103-38-5 4-benzyloxy-3-nitro-aniline 
• 119-27-7 2,4-dinitroanisole 
• 100-51-6 benzyl alcohol 
• 97-02-9 2,4-Dinitroanilin 

Relevant articles and documents

6-Benzyloxyquinazolin-7-ylurea derivatives with an anticancer activity

The present invention relates to a 6-benzyloxyquinazoline-7-ylurea derivative having anticancer activity and, more specifically, to a 6-benzyloxyquinazoline-7-ylurea derivative represented by chemical formula 1 and a compound selected from pharmaceuticall

Nucleophilic Aromatic Substitution in Microemulsions

The rate constants of reaction of 2,4-dinitrofluorobenzene(DNF) with OH- in microemulsions of n-octane, tert-amyl alcohol, and cetyltrimethylammonium bromide (CTABr) and in micelles of CTABr and tert-amyl alcohol can be treated quantitatively by using a pseudophase ion-exchange model and the second-order rate constants in the microemulsion or micelle droplets are larger than that in water, but much smaller than those in moist tertiary alcohols.Reactions of DNF and 2,4-dinitrochlorobenzene (DNC) in microemulsions or micelles containing primary alcohols (n-butyl or benzyl alcohol) give largely ethers as products, and the ethers slowly react giving the 2,4-dinitrophenoxide ion.These reactions of DNF and DNC are faster than reactions with OH- in water but are much slower than those in alcohols.Quantitatively, the relative apparent nucleophilicities of hydroxide and alkoxide ion in the micelle or microemulsion droplet are similar to those in the absence of surfactant.Anionic microemulsions of sodium lauryl sulfate (NaLS) inhibit reactions, but to smaller extent than anionic micelles in water.