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DIETHYL-(4-[2-(4-NITRO-PHENYL)-VINYL]-PHENYL)-AMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65644-11-3

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65644-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65644-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,4 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65644-11:
(7*6)+(6*5)+(5*6)+(4*4)+(3*4)+(2*1)+(1*1)=133
133 % 10 = 3
So 65644-11-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H20N2O2/c1-3-19(4-2)17-11-7-15(8-12-17)5-6-16-9-13-18(14-10-16)20(21)22/h5-14H,3-4H2,1-2H3/b6-5+

65644-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(N,N-diethylamino)-4'-nitrostilbene

1.2 Other means of identification

Product number -
Other names 4-Nitro-4'-N,N-diethylaminostilben

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:65644-11-3 SDS

65644-11-3Relevant academic research and scientific papers

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.

Evidence for two-photon absorption-induced ESIPT of chromophores containing hydroxyl and imino groups

Gao, Fang,Ye, Xiaojuan,Li, Hongru,Zhong, Xiaolin,Wang, Qi

scheme or table, p. 1313 - 1324 (2012/07/14)

This paper presents experimental and theoretical investigations into excited-state intramolecular proton transfer (ESIPT) in new chromophores with hydroxyl and imino groups under one- and two-photon excitation. The results show that internal hydrogen bond

Synthesis and two-photon absorption properties of multi-branched styryl derivatives containing π-bond and σ-electron pair as bridge based on 1,3,5-triazine

Zheng, Zheng,Zhou, Hong-Ping,Xu, Guo-Yi,Yu, Zhi-Peng,Yang, Xiao-Fei,Cheng, Long-Huai,Kong, Lin,Feng, Yan,Wu, Jie-Ying,Tian, Yu-Peng

, p. 6569 - 6574 (2012/09/07)

A series of new one, two, and three-branched two-photon absorption triazine derivatives with a π-bond and a σ-electron pair as a bridge have been synthesized and their photophysical properties have been systematically investigated. These chromophores showed obvious solvatochromic effects, i.e., significant bathochromic shifting of the emission spectra and larger Stokes shifts were observed in more polar solvents mainly due to intra-molecular charge transfer (ICT). The two-photon absorption (2PA) cross-section values were determined by the two-photon excited fluorescence (TPEF) measurements in DMF. This result further proved that a σ-electron pair as a bridge is an efficient way to transfer charge as well as a π bridge, and that their 2PA cross-section values (δ) increase with increasing branch number.

Direct CC Triple Bond Formation from the C=C Double Bond and Direct Hydroxylation into the o-Position of a Nitro Group on the Benzene Nucleus with Potassium t-Butoxide in N,N-DImethylformamide in the Air

Akiyama, Shuzo,Tajima, Kunihiko,Nakatsuji, Shin'ichi,Nakashima, Kenichiro,Abiru, Kazuko,Watanabe, Miwa

, p. 2043 - 2052 (2007/10/03)

A novel and facile method for direct CC acetylenic bond formation from the C=C double bond by treatment with potassium t-butoxide (t-BuOK) in N,N-dimethylformamide in the air has been found in a 9,10-bis(4-substituted styryl)anthracene series, in 4-substituted 4'-nitrostilbene series, and in 1-(p-nitrophenyl)-4-(p-substituted phenyl)-1,3-butadiene series; its scope and limitations have been examined.The ESR spectrum of the reaction against 4-diethylamino-4'-nitrostilbene was measured to identify an anion radical specied expected for explanation of the mechanism of the dehydrogention reaction.Further, cyclic voltammetric measurements of a series of stilbenes and diphenylacetylenes were carried out in connection with the abovw mechanism.In many cases, interestingly, the use of a large excess of t-BuOH brought about succeeding hydroxylation into the ortho-position of a nitro group on the benzene nucleus.The simple hydroxylation is useful for the synthesis of substituted 5-(arylethynyl)-2-nitrophenols, which are expected to function as non-linear optical materials with the corresponding non-hydroxy compounds.The ultraviolet-visible and fluorescence spectral properties were measured and discussed also with those of the related compounds.

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