Welcome to LookChem.com Sign In|Join Free

CAS

  • or
4-Dimethylamino-4'-nitrostilbene, also known as 4-DMANS, is an organic compound with a molecular structure that features a stilbene core with a dimethylamino group at the 4-position and a nitro group at the 4'-position. It is characterized by its unique optical and electronic properties, making it a valuable compound for various applications in scientific research and industry.

2844-15-7 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 2844-15-7 Structure
  • Basic information

    1. Product Name: 4-DIMETHYLAMINO-4'-NITROSTILBENE
    2. Synonyms: 4-DIMETHYLAMINO-4'-NITROSTILBENE;N,N-DIMETHYL-4'-NITRO-4-STILBENAMINE;4-DIMETHYLAMINO-4'-NITROSTILBENE 97%;N,N-Dimethyl-4μ-nitro-4-stilbenamine, DANS;(E)-4-(Dimethylamino)-4'-nitrostilbene;N,N-Dimethyl-4-[(E)-2-(4-nitrophenyl)ethenyl]aniline
    3. CAS NO:2844-15-7
    4. Molecular Formula: C16H16N2O2
    5. Molecular Weight: 268.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2844-15-7.mol
  • Chemical Properties

    1. Melting Point: 256-259 °C(lit.)
    2. Boiling Point: 411.7±24.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.206±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.12±0.15(Predicted)
    10. BRN: 1379389
    11. CAS DataBase Reference: 4-DIMETHYLAMINO-4'-NITROSTILBENE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-DIMETHYLAMINO-4'-NITROSTILBENE(2844-15-7)
    13. EPA Substance Registry System: 4-DIMETHYLAMINO-4'-NITROSTILBENE(2844-15-7)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2844-15-7(Hazardous Substances Data)

2844-15-7 Usage

Uses

Used in Fluorescence Spectroscopy:
4-Dimethylamino-4'-nitrostilbene is used as a standard for the correction of emission in fluorescence spectrometers. Its distinct fluorescence properties and stability make it an ideal reference material for calibrating and optimizing the performance of these instruments, ensuring accurate and reliable measurements in various research and diagnostic applications.
Used in Research and Development:
In the field of research and development, 4-Dimethylamino-4'-nitrostilbene serves as a valuable compound for studying the properties of organic materials, particularly those involving photophysical and photochemical processes. Its unique structure allows scientists to investigate the effects of various functional groups on the compound's behavior, leading to a better understanding of molecular interactions and the development of new materials with tailored properties.
Used in Chemical Synthesis:
4-Dimethylamino-4'-nitrostilbene can also be employed as a starting material or intermediate in the synthesis of more complex organic compounds. Its reactive functional groups make it a versatile building block for the creation of novel molecules with potential applications in various industries, such as pharmaceuticals, materials science, and electronics.
Used in Analytical Chemistry:
In analytical chemistry, 4-Dimethylamino-4'-nitrostilbene can be utilized as a reference compound for the development and validation of new analytical methods and techniques. Its well-defined properties and behavior under various conditions make it an excellent candidate for assessing the performance of new instruments, reagents, and protocols, ultimately contributing to the advancement of analytical science.
Used in Material Science:
The unique optical and electronic properties of 4-Dimethylamino-4'-nitrostilbene make it a promising candidate for the development of new materials with specific characteristics, such as light-emitting diodes (LEDs), solar cells, and sensors. By incorporating this compound into the design of these materials, researchers can potentially enhance their performance and expand their range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2844-15-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,4 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2844-15:
(6*2)+(5*8)+(4*4)+(3*4)+(2*1)+(1*5)=87
87 % 10 = 7
So 2844-15-7 is a valid CAS Registry Number.

2844-15-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Sigma

  • (39255)  4-Dimethylamino-4′-nitrostilbene  ≥99.8% (T)

  • 2844-15-7

  • 39255-500MG

  • 864.63CNY

  • Detail

2844-15-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Dimethylamino-4′-nitrostilbene

1.2 Other means of identification

Product number -
Other names Benzenamine, N,N-dimethyl-4-[2-(4-nitrophenyl)ethenyl]-, (E)-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2844-15-7 SDS

2844-15-7Relevant articles and documents

Nonlinear optical properties of diaromatic stilbene, butadiene and thiophene derivatives

Kukkonen, Esa,Lahtinen, Elmeri,Myllyperki?, Pasi,Haukka, Matti,Konu, Jari

, p. 6640 - 6650 (2021/04/22)

Series of highly polar stilbene (1a-e), diphenylbutadiene (2a-c) and phenylethenylthiophene (3a-c) derivatives were preparedviaHorner-Wadsworth-Emmons method with a view to produce new and efficient materials for second harmonic generation (SHG) in the so

Copper Bis(thiosemicarbazonato)-stilbenyl Complexes That Bind to Amyloid-β Plaques

Cullinane, Carleen,Donnelly, Paul S.,Hayne, David J.,Lim, SinChun,McLean, Catriona A.,Noor, Asif,Roselt, Peter D.,Van Zuylekom, Jessica K.,White, Jonathan M.

, p. 11658 - 11669 (2020/08/24)

Alzheimer's disease is characterized by the presence of extracellular amyloid-β plaques. Positron emission tomography (PET) imaging with tracers radiolabeled with positron-emitting radionuclides that bind to amyloid-β plaques can assist in the diagnosis o

Charge neutral rhenium tricarbonyl complexes of tridentate N-heterocyclic carbene ligands that bind to amyloid plaques of Alzheimer's disease

Barnard, Peter J.,Donnelly, Paul S.,McLean, Catriona A.,Noor, Asif,Wiratpruk, Nuchareenat

supporting information, p. 4559 - 4569 (2020/04/17)

Two tridentate ligand systems bearing N-heterocyclic carbene (NHC), amine and carboxylate donor groups coupled to benzothiazole- or stilbene-based amyloid binding moieties were synthesised. Reaction of the imidazolium salt containing pro-ligands with Re(CO)5Cl yielded the corresponding rhenium metal complexes which were characterised by NMR, and X-ray crystallography. These ligands are of interest for the potential preparation of technetium-99m imaging agents for Alzheimer's disease and the capacity of these rhenium complexes bind to amyloid fibrils composed of amyloid-β peptide and amyloid plaques in human frontal cortex brain tissue was evaluated using fluorescence microscopy. These studies show that the complexes bound efficiently to amyloid-β fibrils and some evidence of binding to amyloid-β plaques.

Molecular probes for imaging of myelin

-

Page/Page column 23; 28-30, (2018/06/18)

A molecular probe for labeling myelin includes a fluorescent trans-stilbene derivative.

Theoretical and Experimental Studies of N,N-Dimethyl-N′-Picryl-4,4′-Stilbenediamine

Papper, Vladislav,Wu, Yuanyuan,Kharlanov, Vladimir,Sukharaharja, Ayrine,Steele, Terry W. J.,Marks, Robert S.

, p. 13 - 19 (2015/02/19)

N,N-dimethyl-N′-picryl-4,4′-stilbenediamine (DMPSDA) was prepared, purified and crystallised in a form of black lustrous crystals, and its absorption and fluorescence spectra were recorded in cyclohexane, acetonitrile and dimethyl sulfoxide. Non-emissive

Rhenium(i) complexes of N-heterocyclic carbene ligands that bind to amyloid plaques of Alzheimer's disease

Chan, Chung Ying,Noor, Asif,McLean, Catriona A.,Donnelly, Paul S.,Barnard, Peter J.

supporting information, p. 2311 - 2314 (2017/02/23)

A series of [Re(i)L(CO)3]+ complexes (where L is a bifunctional bis(NHC)-amine ligand) that are analogues of potential Tc-99m diagnostic imaging agents for Alzheimer's disease have been synthesised. One of the complexes bound to amyl

New organic conjugated dye nano-aggregates exhibiting naked-eye fluorescence color switching

Ding, Ge,Lu, Yao,Qin, Xiaozhuan,Su, Jihong,Zhang, Shengtao,Li, Hongru,Luo, Ziping,Chen, Lingyun,Gao, Fang

, p. 19 - 32 (2016/12/26)

In this study, a variety of new conjugated containing strong electron-donating groups were prepared for formation of organic nano-scale aggregates. The properties and aggregation modes of these aggregates were investigated on basis of time dependent absorption, fluorescence emission spectra as well as scanning electron microscope images. The results show that nano organic aggregates could be yielded by the linear dyes in mixed DMF/H2O solvent through a simple re-precipitation method, while no aggregates of the branched dyes were produced. X-ray diffraction of single crystal and X-ray diffraction patterns of the powders results demonstrate that the linear dyes tend to show ordered molecular arrangements, while the armed dyes do not exhibit such a tendency. A remarkable fluorescence switching process under 365 nm lamp was observed for the target aggregates. This study successfully provides real examples of organic aggregates in mixed DMF/H2O solvent which have great capacity to show enhanced fluorescence color switching.

Fluorescent gelators for detection of explosives

Hanabusa, Kenji,Takata, Shingo,Fujisaki, Masafumi,Nomura, Yasushi,Suzuki, Masahiro

, p. 1391 - 1401 (2017/08/02)

Carbazole-, quinoline-, benzothiazole-, and stilbene-containing fluorescent gelators are synthesized by connecting gelationdriving segments, and their gelation abilities are studied with 13 solvents. Fibrous thin-layer films are prepared on quartz plates

Solvatochromic behavior of dyes with dimethylamino electron-donor and nitro electron-acceptor groups in their molecular structure

De Melo, Carlos E. A.,Nandi, Leandro G.,Domínguez, Moisés,Rezende, Marcos C.,Machado, Vanderlei G.

, p. 250 - 260 (2015/03/31)

Six dyes with N,N-dimethylaminophenyl and 4-nitrophenyl or 2,4-dinitrophenyl groups in their molecular structures were prepared and characterized. These compounds have different conjugated bridges (C-C, C-N, and N-N) connecting the electron-donor and the electron-acceptor groups. All compounds are solvatochromic, with reverse solvatochromism occurring. The solvatochromic band observed in each spectrum for the dyes is due to a π rarr π? transition, of an intramolecular charge transfer nature, which occurs from the electron-donor N,N-dimethylaminophenyl group to the electron-acceptor group in the molecules, which is reinforced by the structures of the compounds optimized by applying density functional theory, which exhibit high planarity. The reverse solvatochromism was explained considering two resonance structures. The benzenoid form is better stabilized in less polar solvents and characterizes the region displaying positive solvatochromism, while the dipolar form is better stabilized in more polar solvents, in the region of negative solvatochromism. The Catalán multiparametric approach was used to study the contribution of solvent acidity, basicity, dipolarity, and polarizability to the solvatochromism exhibited by the compounds. These compounds are good candidates for the investigation of the polarizability and, to a lesser extent, the dipolarity of the medium, with very little interference from specific interactions of the solvent through hydrogen bonding.

Evaluating two new Schiff bases synthesized on the inhibition of corrosion of copper in NaCl solutions

Zhou, Yang,Xu, Shenying,Guo, Lei,Zhang, Shengtao,Lu, Hao,Gong, Yulong,Gao, Fang

, p. 14804 - 14813 (2015/03/05)

Two kinds of new Schiff base derivatives, 2-((4-(4-(dimethylamino)styryl)phenylimino)methyl) (DSM) and its intermediate 4-(4-aminostyryl)-N,N-dimethylaniline (AND), form self-assembled monolayers (SAMs) on copper surfaces. The SAMs have been examined by a series of techniques, including contact angle (CA), atomic force microscope (AFM), scanning electronic microscope (SEM), and electrochemical measurements. The results suggest that the two derivatives adsorb onto the copper surface and generate corresponding hydrophobic films, which play an important role in the anticorrosion of copper in 3% NaCl solution. Quantum chemical calculations and molecular dynamics (MD) simulation are also used for further insight into the adsorption mechanism.

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

What can I do for you?
Get Best Price

Get Best Price for 2844-15-7