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17573-94-3

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17573-94-3 Usage

Uses

4-Ethynyl-N,N-dimethylaniline may be used to synthesize the following:copper(I) arylacetylide via reaction with copper(II)acetateN,N-dimethyl-4-(3-pyridinylethynyl)aniline via Sonogashira–Hagihara coupling with 3-iodopyridine[[5,15-bis[(40-dimethylamino)phenyl]ethynyl]-10,20-bis[(triisopropylsilyl)ethynyl]porphyrinato]magnesium(II) via reaction with dibromo magnesium porphyrin

General Description

4-Ethynyl-N,N-dimethylaniline can be prepared via hydrolysis of 4-(3-methyl-3-hydroxy-1-butynyl)-N,N-dimethylaniline using potassium hydroxide in toluene.

Check Digit Verification of cas no

The CAS Registry Mumber 17573-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,7 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17573-94:
(7*1)+(6*7)+(5*5)+(4*7)+(3*3)+(2*9)+(1*4)=133
133 % 10 = 3
So 17573-94-3 is a valid CAS Registry Number.

17573-94-3 Well-known Company Product Price

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  • Aldrich

  • (592609)  4-Ethynyl-N,N-dimethylaniline  97%

  • 17573-94-3

  • 592609-1G

  • 774.54CNY

  • Detail
  • Aldrich

  • (592609)  4-Ethynyl-N,N-dimethylaniline  97%

  • 17573-94-3

  • 592609-5G

  • 2,844.27CNY

  • Detail

17573-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4'-DIMETHYLAMINOPHENYL ACETYLENE

1.2 Other means of identification

Product number -
Other names N,N-dimethyl-4-ethynylaniline

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:17573-94-3 SDS

17573-94-3Relevant articles and documents

Benzobisimidazole Cruciform Fluorophores

Le, Ha T. M.,El-Hamdi, Nadia S.,Miljani?, Ognjen ?.

, p. 5210 - 5217 (2015)

A series of 11 cross-conjugated cruciform fluorophores based on a benzobisimidazole nucleus has been synthesized and characterized. Like in their previously reported benzobisoxazole counterparts, the HOMOs of these new fluorophores are localized along the vertical bisethynylbenzene axes, while their LUMOs remain relatively delocalized across the molecule, except in cruciforms substituted with electron-withdrawing groups along the vertical axis. Benzobisimidazole cruciforms exhibit a pronounced response to deprotonation in their UV/vis absorption and emission spectra, but their response to protonation is significantly attenuated. (Chemical Equation Presented).

A Porous and Solution-Processable Molecular Crystal Stable at 200 °c: The Surprising Donor-Acceptor Impact

Cheng, Shengxian,Ma, Xiaoxia,He, Yonghe,He, Jun,Zeller, Matthias,Xu, Zhengtao

, p. 7411 - 7419 (2019)

We report a curious porous molecular crystal that is devoid of the common traits of related systems. Namely, the molecule does not rely on directional hydrogen bonds to enforce open packing, and it offers neither large concave faces (i.e., high internal f

Synthesis, Crystal Structures, and Solid-State Polymerization of 8?[4-(Dimethylamino)phenyl]octa-5,7-diynyl Carbamates

Ikeshima, Masataka,Katagiri, Hiroshi,Fujiwara, Wataru,Tokito, Shizuo,Okada, Shuji

, p. 5991 - 6000 (2018)

Six butadiyne monomers with (dimethylamino)phenyl and N-substituted urethane substituents were synthesized and their crystal structures and solid-state polymerization were investigated. In five of the six monomers, directions of the butadiyne stacking and

Synthesis and Solid-State Polymerization of 4-(Dimethylamino) phenylbutadiyne Derivatives and Their Charge-Transfer Complexes

Ishii, Shinji,Kaneko, Shota,Tatewaki, Yoko,Okada, Shuji

, p. 64 - 68 (2013)

(Five urethane derivatives of 8-[4-(dimethylamino)phenyl]octa-5,7-diyn-1-ol were synthesized. They could be polymerized in the solid state to give conjugated backbones although structural regularity seemed to be not so high. Formability of chargetransfer

Combinatorial synthesis of new fluorescent scaffolds using click chemistry

Cleemann, Felix,Karuso, Peter,Kum-Cheung, Wendy Loa

supporting information, (2021/12/08)

Azides and acetylenes are bio-orthogonal functional groups that can be readily coupled using copper(I)- or ruthenium(II)- catalyzed 1,3-dipolar cycloaddition reactions. Using non-fluorescent aromatic azides and aromatic acetylenes, covering a range of electron rich and poor building blocks, the Huisgen cycloaddition afford 1,4-disubstituted or 1,5-disubstituted 1,2,3-triazoles. Using a combinatorial approach by running reaction in parallel in polypropylene 96-well plates we discovered several new fluorescent 1,2,3-triazoles scaffolds. These compounds show diverse interactions with biomolecules that could find applications in biology in, for example, fluorescence microscopy or biomolecule quantification.

Near-Infrared Fluorescent Probes with Rotatable Polyacetylene Chains for the Detection of Amyloid-β Plaques

Zhang, Longfei,Gong, Xin,Tian, Chuan,Fu, Hualong,Tan, Hongwei,Dai, Jiapei,Cui, Mengchao

, p. 497 - 506 (2021/01/26)

The plaques of accumulated β-amyloid (Aβ) in the parenchymal brain are accepted as an important biomarker for the early diagnosis of Alzheimer's disease (AD). Many near-infrared (NIR) probes, which were based on the D-π-A structure and bridged by conjugat

Donor-acceptor substituted benzo-, naphtho- and phenanthro-fused norbornadienes

Fernandez, Lorette,Mans?, Mads,Moth-Poulsen, Kasper,Nielsen, Mogens Br?ndsted,Wang, Zhihang

, (2020/01/31)

The photochromic norbornadiene/quadricyclane (NBD/QC) couple has found interest as a molecular solar thermal energy (MOST) system for storage of solar energy. To increase the energy difference between the two isomers, we present here the synthesis of a selection of benzo-fused NBD derivatives that contain an aromatic unit, benzene, naphthalene or phenanthrene, fused to one of the NBD double bonds, while the carbon atoms of the other double bond are functionalized with donor and acceptor groups. The synthesis protocols involve functionalization of benzo-fused NBDs with bromo/chloro substituents followed by a subjection of these intermediates to a cyanation reaction (introducing a cyano acceptor group) followed by a Sonogashira coupling (introducing an arylethynyl donor group, -C≡CC6H4NMe2 or -C≡CC6H4OMe). While the derivatives have good absorption properties in the visible region (redshifted relative to parent system) in the context of MOST applications, they lack the ability to undergo NBD-to-QC photoisomerization, even in the presence of a photosensitizer. It seems that loss of aromaticity of the fused aromatics is too significant to allow photoisomerization to occur. The concept of destroying aromaticity of a neighboring moiety as a way to enhance the energy density of the NBD/QC couple thus needs further structural modifications, in the quest for optimum MOST systems.

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