610-54-8 Usage
Description
2,4-DINITROPHENETOLE, also known as an aromatic ether, is a chemical compound that consists of phenetole substituted at the C-2 and C-4 positions by nitro groups. It is characterized by its aromatic structure and the presence of nitro groups, which contribute to its unique properties and potential applications.
Uses
Used in Chemical Synthesis:
2,4-DINITROPHENETOLE is used as an intermediate in the synthesis of various organic compounds. Its aromatic ether structure and nitro-substituted positions make it a valuable building block for creating a wide range of chemical products, including pharmaceuticals, agrochemicals, and dyes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,4-DINITROPHENETOLE is used as a key component in the development of new drugs. Its unique chemical structure allows it to interact with specific biological targets, making it a promising candidate for the treatment of various diseases and medical conditions.
Used in Dye Manufacturing:
2,4-DINITROPHENETOLE is used as a starting material in the production of dyes. Its aromatic structure and nitro groups contribute to the color properties of the resulting dyes, making it an essential component in the dye manufacturing process.
Used in Agrochemicals:
In the agrochemical industry, 2,4-DINITROPHENETOLE is used as a precursor for the development of new pesticides and herbicides. Its chemical properties enable it to be modified and functionalized to create compounds with specific pesticidal or herbicidal activities, helping to improve crop protection and yield.
Used in Research and Development:
2,4-DINITROPHENETOLE is also used in research and development for its potential applications in various fields. Its unique chemical structure makes it an interesting subject for studying its properties, reactivity, and potential uses in different industries, including materials science, environmental science, and nanotechnology.
Purification Methods
Crystallise it from aqueous EtOH. The 1:1 naphthalene complex has m 41o and is obtained by fusing the compound with naphthalene in various ratios, then crystallizing the solidified mix with a little EtOH (Dermer & Smith J Am Chem Soc 61 748 1939). [Beilstein 6 H 254, 6 III 858, 6 IV 1373.]
Check Digit Verification of cas no
The CAS Registry Mumber 610-54-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 610-54:
(5*6)+(4*1)+(3*0)+(2*5)+(1*4)=48
48 % 10 = 8
So 610-54-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O5/c1-2-15-8-4-3-6(9(11)12)5-7(8)10(13)14/h3-5H,2H2,1H3
610-54-8Relevant articles and documents
SNAr reactions of 1-halo-2,4-dinitrobenzenes with alkali-metal ethoxides: Differential stabilization of ground state and transition state determines alkali-metal ion catalysis or inhibition
Yang, Kiyull,Kim, Min-Young,Um, Ik-Hwan
, p. 1812 - 1818 (2015)
A kinetic study on SNAr reactions of 1-halo-2,4-dinitrobenzenes (6a-6d) with alkali-metal ethoxides (EtOM; M = Li, Na, K and 18-crown-6-ether-complexed K) is reported. The plots of pseudo-first-order rate constant (kobsd) vs. [EtOM]
Rationalising the effects of ionic liquids on a nucleophilic aromatic substitution reaction
Hawker, Rebecca R.,Wong, Michaela J.,Haines, Ronald S.,Harper, Jason B.
supporting information, p. 6433 - 6440 (2017/08/10)
The nucleophilic aromatic substitution reaction between 1-fluoro-2,4-dinitrobenzene and ethanol was examined in a series of ionic liquids across a range of mole fractions. Temperature-dependent kinetic analyses were undertaken to determine the activation parameters for this reaction at the highest mole fraction. As the mole fraction of ionic liquid was increased, the rate constant of the reaction also increased, however the microscopic origin of the rate enhancement was shown to be different between different ionic liquids and also between different solvent compositions. These results indicate a balance between microscopic interactions that result in the observed solvent effects and a qualitative method for analysing such interactions is introduced.
Novel Chloroimidazolium-Based Ionic Liquids: Synthesis, Characterisation and Behaviour as Solvents to Control Reaction Outcome
Hawker, Rebecca R.,Panchompoo, Janjira,Aldous, Leigh,Harper, Jason B.
, p. 574 - 583 (2016/07/06)
Novel ionic liquids containing chlorine atoms on the imidazolium cation were synthesised. The physicochemical properties of these ionic liquids were investigated extensively, including glass transition, melting and decomposition temperatures, density, vis
