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5,11,17,23-tetrakis<(p-carboxyphenyl)azo>-25,26,27,28-tetrahydroxycalix<4>arene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125583-12-2

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125583-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125583-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,5,8 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125583-12:
(8*1)+(7*2)+(6*5)+(5*5)+(4*8)+(3*3)+(2*1)+(1*2)=122
122 % 10 = 2
So 125583-12-2 is a valid CAS Registry Number.

125583-12-2Downstream Products

125583-12-2Relevant academic research and scientific papers

A Noncovalent Fluorescence Turn-on Strategy for Hypoxia Imaging

Geng, Wen-Chao,Jia, Shaorui,Zheng, Zhe,Li, Zhihao,Ding, Dan,Guo, Dong-Sheng

, p. 2377 - 2381 (2019)

Hypoxia plays crucial roles in many diseases and is a central target for them. Present hypoxia imaging is restricted to the covalent approach, which needs tedious synthesis. In this work, a new supramolecular host–guest approach, based on the complexation

Antiradical and antioxidative activity of azocalix[4]arene derivatives: Combined experimental and theoretical study

Ni, Jiaqi,Lu, Lilin,Liu, Yi

, (2019)

Developing antioxidants with high efficiency is fundamentally important for the protection of living cells and engineering materials against oxidative damage. In this present study, two azocalix[4]arene derivatives were synthesized via a diazo coupling re

Synthesis and spectral characterization of azo dyes derived from calix[4]arene and their application in dyeing of fibers

Elcin, Serkan,Ilhan, Murat Muzaffer,Deligoez, Hasalettin

, p. 259 - 267 (2013)

In this study, the synthesis and characterization of two new upper rim functionalized azocalix[4]arene dyes have been obtained by coupling calix[4]arene with different diazo compounds of 3,5-dicarboxyaniline and 4-aminobenzene sulphon amide. The character

5,11,17,23-tetrakis[(p-carboxyphenyl)azo]-25,26,27,28-tetrahydroxy calix[4]arene: Crystal structure and pH sensing properties

Liu, Leilei,Ren, Zhigang,Li, Hongxi,Shang, Hai,Lang, Jianping

, p. 1829 - 1834 (2010)

Treatment of 5,11,17,23-tetrakis[(p-carboxyphenyl)azo]-25,26,27,28-tetrahydroxy calix[4]arene (2) with HCl in DMF or NaOH in MeOH produced 5,11,17,23-tetrakis[(p-carboxyphenyl)azo]-25,26,27,28-tetrahydroxycalix[4]-arene·4DMF (2·4DMF) and 5,11,17,23-tetrak

Azocalix[4]arene-rhodamine supramolecular hypoxia-sensitive systems: A search for the best calixarene hosts and rhodamine guests

Antipin, Igor,Burilov, Vladimir,Galieva, Farida,Gazalieva, Alsu,Khalifa, Mohamed Ali Mohamed,Kleshnina, Sofia,Mironova, Diana,Nugmanov, Ramil,Solovieva, Svetlana

, (2021/09/13)

A potential hypoxia-sensitive system host-guest complex of three calixarenes (including two with four anionic carboxyl and sulphonate azo fragments on the upper rim and a newly synthesized bis-azo adduct of calixarene in the cone configuration with azo fr

Dissociation dynamics of host-guest interaction between substituted calix[4]-arene and 4-chloronitrobenzene

Kumar, Ashok,Sharma, Pratibha,Sharma, Pawan Kumar,Ahuja, Monika,Matisz, Gergely,Kollar, Laszlo,Sandor, Kunsagi-Mate

, p. 304 - 308 (2017/08/04)

The inclusion complexation of upper rim substituted calix[4]arene with neutral 4-chloronitrobenzene has been studied by quantum-chemical and spectrophotometric measurements. The effect of varying temperature on the formation versus dissociation of the hos

Quasi-solid-state rechargeable lithium-ion batteries with a calix[4]quinone cathode and gel polymer electrolyte

Huang, Weiwei,Zhu, Zhiqiang,Wang, Lijiang,Wang, Shiwen,Li, Hao,Tao, Zhanliang,Shi, Jifu,Guan, Lunhui,Chen, Jun

supporting information, p. 9162 - 9166 (2013/09/12)

Filled to capacity: Calix[4]quinone (C4Q) has eight available carbonyl groups for binding lithium ions (see picture). It can be exploited to prepare quasi-solid-state rechargeable lithium batteries with a poly(methyl acrylate)/poly(ethylene glycol) based

Synthesis and study of binuclear calix[4]arene Schiff base Mn(II) complexes as catalyst in the presence of PhIO for the catalytic oxidation of olefin

Patel, Ravindra V.,Panchal, Jayesh G.,Mistry, Bhoomika R.,Menon, Shobhana K.

scheme or table, p. 473 - 480 (2012/10/08)

The binuclear Mn(II) complexes of calix[4]arene substituted 2-vanillin and 2-hydroxy naphthaldimine, Schiff bases (Mn2L1 and Mn 2L2) have been synthesized, characterized and employed as models to mimic monooxyge

Synthesis and study of binuclear calix[4]arene Schiff base Co(II) complexes as catalyst in the presence of PhIO for the catalytic oxidation of olefin

Patel, Ravindra V.,Panchal, Jayesh G.,Menon, Shobhana K.

scheme or table, p. 63 - 71 (2011/10/30)

The binuclear Co(II) complexes of calix[4]arene substituted 2-vanillin (R1) and 2-hydroxy naphthaldimine (R2), Schiff bases (Co2L1 and Co2L2) have been synthesized, characterized and employ

Liquid crystals based on calix[4]arene Schiff bases

Patel, Ravindra V.,Panchal, Jayesh G.,Rana,Menon, Shobhana K.

scheme or table, p. 285 - 295 (2011/12/16)

New liquid crystals based on calix[4]arene Schiff base were prepared by the reaction of tetraamino-calix[4]arene with aldehydes (4-hydroxy benzaldehyde, 2-vanillin, 4-vanillin and 2-hydroxy naphthaldehyde). Dielectric investigations on a magnetically oriented sample forming N, SmA, and SmC phases were carried out. The dielectric constant (ε' and ε) and dielectric loss (tan δ) have been determined as a function of frequency (20 Hz-2 MHz). The synthesized derivatives were purified and characterized by FT-IR, 1H-NMR, 13C-NMR and MALDI-TOF MS. All the synthesized compounds were investigated for liquid crystalline properties using DSC (Differential Scanning Calorimetry), DTA (Differential Thermal Analysis) and POM (Polarizing Optical Microscopy) attached with a hot stage. They generally exhibited nematic and typical fanlike or mosaic texture, which suggest the ordered smectic mesophases. Compounds were found to adopt a specific molecular structure due to the rigid bowl like calix[4]arene core, i.e., a cone-like structure with mesogenic units aligned within the molecule.

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