Welcome to LookChem.com Sign In|Join Free
  • or
(2,4-diaminophenyl)is a chemical compound that features a phenyl ring with two amino groups (NH2) attached at the 2nd and 4th positions of the ring. This structure endows it with versatile reactivity, allowing it to engage in various chemical reactions such as nucleophilic substitution, aromatic electrophilic substitution, and condensation reactions. Its unique properties make it a valuable intermediate in the synthesis of a wide range of organic compounds, including dyes, pharmaceuticals, and polymers.

7450-55-7

Post Buying Request

7450-55-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7450-55-7 Usage

Uses

Used in Pharmaceutical Industry:
(2,4-diaminophenyl)serves as a key building block in the development of pharmaceuticals due to its ability to form a variety of chemical bonds and its compatibility with different molecular structures. Its presence in drug molecules can enhance their therapeutic effects and improve their pharmacokinetic properties.
Used in Dye Industry:
As a component in dye synthesis, (2,4-diaminophenyl)contributes to the creation of a broad spectrum of colors and shades. Its chemical versatility allows for the production of dyes with specific properties, such as light-fastness, wash-fastness, and resistance to fading.
Used in Polymer Industry:
(2,4-diaminophenyl)is utilized in the synthesis of polymers to introduce specific functional groups and properties. Its incorporation can lead to the development of polymers with enhanced mechanical strength, thermal stability, or chemical resistance, depending on the desired application.
Used in Chemical Intermediates:
(2,4-diaminophenyl)acts as an important intermediate in the production of numerous commercial products and materials. Its unique structure and reactivity make it a crucial component in the synthesis of various organic compounds, contributing to the development of new technologies and innovations across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 7450-55-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,5 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7450-55:
(6*7)+(5*4)+(4*5)+(3*0)+(2*5)+(1*5)=97
97 % 10 = 7
So 7450-55-7 is a valid CAS Registry Number.

7450-55-7Downstream Products

7450-55-7Relevant academic research and scientific papers

A rapid, facile and green synthesis of Ag@AgCl nanoparticles for the effective reduction of 2,4-dinitrophenyl hydrazine

Devi, Th. Babita,Ahmaruzzaman,Begum, Shamima

, p. 1497 - 1506 (2016)

In this study, we have developed a green and single-step process for the fabrication of Ag@AgCl nanoparticles (NPs) using the leaf extract of Momordica charantia. This method does not require the utilization of any surfactant/halide source or external ene

Green synthesis of a Cu/MgO nanocomposite by: Cassytha filiformis L. extract and investigation of its catalytic activity in the reduction of methylene blue, congo red and nitro compounds in aqueous media

Nasrollahzadeh, Mahmoud,Issaabadi, Zahra,Sajadi, S. Mohammad

, p. 3723 - 3735 (2018)

This work reports the green synthesis of a Cu/MgO nanocomposite using Cassytha filiformis L. extract as a reducing agent without stabilizers or surfactants. The immobilization of Cu NPs was confirmed by Fourier transform infrared spectroscopy (FT-IR), X-r

A novel magnetic starch nanocomposite as a green heterogeneous support for immobilization of Cu nanoparticles and selective catalytic application in eco-friendly media

Khalilzadeh, Mohammad A.,Nasiri, Atefeh,Zareyee, Daryoush

, (2021/10/01)

In this work, Stipa capensis extract mediated the synthesis of Cu nanoparticles (Cu NPs) and their immobilization on the surface of nanostarch-coated Fe3O4. The prepared nanocatalyst (Cu NPs@Fe3O4-nanostarch) wa

High catalytic activity of a new Ag phosphorus ylide complex supported on montmorillonite: synthesis, characterization, and application for room temperature nitro reduction

Karami, Kazem,Rahimi, Mahzad,Dinari, Mohammad

, p. 281 - 291 (2018/03/29)

In this work, the phosphorus ylide, [PPh3CHC(O)CH2Cl], was reacted with AgNO3 to give the [Ag{C(H)PPh3C(O)CH2Cl}2]+NO3? as the product. Then, it was supported on the modified montmorillonite nanoclay to prepare a new catalyst for the reduction reaction. The structure and morphology of the nanoclay catalyst were characterized by FT-IR, X-ray powder diffraction, scanning electron microscopy, energy-dispersive X-ray analysis and transmission electron microscopy techniques; also, the content of silver was obtained by inductively coupled plasma analyzer. This composition was exploited to study its catalytic activity in the reduction in aromatic nitro compounds; it displayed the high catalytic activity. Factors such as catalyst amount, solvent, temperature and reaction time were all systematically investigated to elucidate their effects on the yield of catalytic reduction in nitroarenes. This catalytic system exhibited high activity toward aromatic nitro compounds under mild conditions. The catalyst was reused five times without any significant loss in its catalytic activity.

Experimental and quantum chemical study on nano-copper immobilized on magnetic graphitic carbon nitride core shell particles; a reusable heterogeneous catalyst toward reduction of nitro arenes

-

, (2019/03/05)

A new magnetic material, which named CuFe2O4?SiO2?g-C3N4/Cu with a core/shell morphology has been designed and synthesized. For the first time ever, the mixture of carbon and g-C3N4 layer was applied as an effective linker for immobilization of Cu metal on the catalyst. The physiochemical properties of the catalyst were identified by XRD, FT-IR, VSM, FE-SEM and TEM characterization techniques. The reduction of nitro compounds to the corresponding amines was investigated in the presence of NaBH4 at 55 °C in water. Quantum chemical study reveals that the addition of Cu atoms to the g-C3N4 layer induce a slight structural deformation via changing the bond lengths and bond orders, also the type of interaction of Cu atoms and nitrogen atoms of g-C3N4 is mainly electrostatic in nature. Induced pattern of charge distribution provided by Electrostatic Potential Map exhibits the attractive regions for electrophiles and nucleophiles interacting with this system.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 7450-55-7