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57341-98-7

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57341-98-7 Usage

General Description

4-(2-phenyleth-1-ynyl)benzaldehyde is a chemical compound with the formula C15H10O. It is a pale yellow liquid that is insoluble in water but soluble in organic solvents. 4-(2-PHENYLETH-1-YNYL)BENZALDEHYDE is used in the synthesis of various pharmaceuticals, agrochemicals, and materials due to its aromatic properties and potential as a building block for other organic compounds. It is also utilized in organic electronic devices and as an intermediate in the production of fragrances and flavors. The aldehyde group in 4-(2-phenyleth-1-ynyl)benzaldehyde makes it a versatile ingredient in organic synthesis and a useful starting material for the preparation of a wide range of compounds. Overall, this chemical has multiple applications in various industries due to its unique and versatile properties.

Check Digit Verification of cas no

The CAS Registry Mumber 57341-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,4 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57341-98:
(7*5)+(6*7)+(5*3)+(4*4)+(3*1)+(2*9)+(1*8)=137
137 % 10 = 7
So 57341-98-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O/c16-12-15-10-8-14(9-11-15)7-6-13-4-2-1-3-5-13/h1-5,8-12H

57341-98-7SDS

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-(2-phenylethynyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-(2-phenylethynyl)-benzaldehyde

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:57341-98-7 SDS

57341-98-7Relevant articles and documents

HBC-porphyrin-close contact chromophores

Englert, Jan M.,Malig, Jenny,Zamolo, Valeria Anna,Hirsch, Andreas,Jux, Norbert

, p. 4827 - 4829 (2013)

A photo/redoxactive hexa-peri-hexabenzocoronene-porphyrin conjugate with a direct connection between the two chromophores was synthesised using a formylated hexaphenylbenzene precursor.

Synthesis of new styrylquinoline cellular dyes, fluorescent properties, cellular localization and cytotoxic behavior

Rams-Baron, Marzena,Dulski, Mateusz,Mrozek-Wilczkiewicz, Anna,Korzec, Mateusz,Cieslik, Wioleta,Spaczyńska, Ewelina,Bartczak, Piotr,Ratuszna, Alicja,Polanski, Jaroslaw,Musiol, Robert

, (2015)

New styrylquinoline derivatives with their photophysical constants are described. The synthesis was achieved via Sonogashira coupling using the newly developed heterogeneous nano-Pd/Cu catalyst system, which provides an efficient synthesis of high purity

A Reversible Rhodamine B Based pH Probe with Large Pseudo-Stokes Shift

Bao, Guochen,Wong, Ka-Leung,Tanner, Peter A.

, p. 816 - 820 (2019)

A reversible and sensitive pH probe DPE?Rh operates by F?rster resonance energy transfer from 1,2-diphenylethyne (DPE) to Rhodamine B (Rh). In the presence of H+, the spirolactam ring of the Rhodamine B unit was opened and this resulted in ca. 1000-fold enhancement of fluorescence intensity with linear change over the pH range of 2.0 to 5.5. The F?rster resonance energy transfer offered this probe an effective excitation–emission wavelength shift of around 240 nm with about 100 % quenching of the donor emission. The response of the sensor is tolerant towards a wide range of metal ions and the sensing mechanism was deduced by 1H NMR spectrometry. This FRET-based molecule not only provides a sensitive pH probe, but also suggests an effective strategy to eliminate the interference of excitation light.

ERRγ ligand HPB2 upregulates BDNF-TrkB and enhances dopaminergic neuronal phenotype

Kim, Hyo In,Lee, Seungbeom,Lim, Juhee,Chung, Sungkyun,Koo, Tae-Sung,Ji, Yu-Geun,Suh, Young-Ger,Son, Woo Sung,Kim, Seok-Ho,Choi, Hyun Jin

, (2021)

Brain derived neurotrophic factor (BDNF) promotes maturation of dopaminergic (DAergic) neurons in the midbrain and positively regulates their maintenance and outgrowth. Therefore, understanding the mechanisms regulating the BDNF signaling pathway in DAerg

Zeolitic imidazolate frameworks-67 (ZIF-67) supported PdCu nanoparticles for enhanced catalytic activity in Sonogashira-Hagihara and nitro group reduction under mild conditions

Gholinejad, Mohammad,Naghshbandi, Zhwan,Sansano, Jose M.

, (2022/01/11)

A bimetallic PdCu supported on amine functionalized ZIF-67 is shown to be efficient catalyst in Sonogashira-Hagihara coupling reaction of aryl iodides at room temperature and aryl bromides at 40 oC. In addition, the catalyst is used in the reduction of 4-

Metal scavenging and catalysis by periodic mesoporous organosilicas with 2,2′-bipyridine metal chelating ligands

Waki, Minoru,Inagaki, Shinji

, (2021/06/21)

A periodic mesoporous organosilica containing 2,2′-bipyridine (BPy-PMO) was assessed as a metal scavenger and heterogeneous catalyst. The functionalized PMO was synthesized based on a modified version of a previously reported procedure and showed a large

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