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59156-21-7

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59156-21-7 Usage

General Description

2-(4-Nitrophenyl)thiophene is a chemical compound with the molecular formula C10H7NO2S. It is a member of the thiophene family, which is a group of aromatic heterocyclic compounds containing a five-membered sulfur-containing ring. The presence of a nitro group in the phenyl ring makes this compound highly reactive and useful in various chemical reactions, particularly in the synthesis of other complex organic molecules. It also exhibits interesting electronic and optical properties, making it potentially useful in materials science and organic electronics. Additionally, the nitro group can be reduced to an amino group, providing the potential for further functionalization and diversification of its chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 59156-21-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,5 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59156-21:
(7*5)+(6*9)+(5*1)+(4*5)+(3*6)+(2*2)+(1*1)=137
137 % 10 = 7
So 59156-21-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H7NO2S/c12-11(13)9-5-3-8(4-6-9)10-2-1-7-14-10/h1-7H

59156-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Nitrophenyl)thiophene

1.2 Other means of identification

Product number -
Other names 1-(thien-2-yl)-4-nitrobenzene

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:59156-21-7 SDS

59156-21-7Relevant articles and documents

Tunable electrochemical switches based on ultrathin organic films

Fave, Claire,Leroux, Yann,Trippe, Gaelle,Randriamahazaka, Hyacinte,Noel, Vincent,Lacroix, Jean-Christophe

, p. 1890 - 1891 (2007)

We have performed electroreduction of bisthienyl aminobenzene and thienyl aminobenzene diazonium salts on glassy carbon and polycrystalline gold and generated ultrathin organic films. This method allows covalent bonding between the corresponding aromatic

Triphenylamine derivatives and the lithium-ion capture of [3.3]cyclophane used in organic dye-sensitized solar cells

Chiu, Yu-Hsiang,Shibahara, Masahiko,Huang, Rui-Yu,Watanabe, Motonori,Wang, Zhong-Sheng,Hsiao, Yu-Jen,Chang, Bo-Fong,Chiang, Ting-Hsuan,Chang, Yuan Jay

, p. 761 - 772 (2017)

Four novel organic dyes (H-1, H-2, H-3, H-4) containing phenyl-thiophenyl-thiophenyl as a bridge unit were synthesized and effectively used for the fabrication of dye-sensitized solar cells (DSSCs). In both compounds, a triarylamine moiety and cyanoacryli

Identification of Piperidine-3-carboxamide Derivatives Inducing Senescence-like Phenotype with Antimelanoma Activities

Oh, Sangmi,Kwon, Do Yoon,Choi, Inhee,Kim, Young Mi,Lee, Ji Young,Ryu, Jiyoung,Jeong, Hangyeol,Kim, Myung Jin,Song, Rita

, p. 563 - 571 (2021/05/06)

This study evaluated the potential use of senescence-inducing small molecules in the treatment of melanoma. We screened commercially available small-molecule libraries with high-throughput screening and high-content screening image-based technology. Our findings showed an initial hit with the embedded N-arylpiperidine-3-carboxamide scaffold-induced senescence-like phenotypic changes in human melanoma A375 cells without serious cytotoxicity against normal cells. A focused library containing diversely modified analogues were constructed and examined to evaluate the structure-activity relationship of N-arylpiperidine-3-carboxamide derivatives starting from hit 1. This work identified a novel compound with remarkable antiproliferative activity in vitro and demonstrated the key structural moieties within.

UiO-66 microcrystals catalyzed direct arylation of enol acetates and heteroarenes with aryl diazonium salts in water

Sun, Zhong-Hua,Chen, Wang,Qian, Bing-Bing,Wang, Liang,Yu, Binxun,Chen, Qun,He, Ming-Yang,Zhang, Zhi-Hui

, (2020/01/25)

UiO-66 is a classic Metal–organic framework (MOF) that constructed by zirconium cations and terephthalate with high chemical and thermal stability. Using pristine UiO-66 nanocrystals as the catalysts, the carbon–carbon bond formation based on denitrogenat

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