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252771-08-7

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252771-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 252771-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,7,7 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 252771-08:
(8*2)+(7*5)+(6*2)+(5*7)+(4*7)+(3*1)+(2*0)+(1*8)=137
137 % 10 = 7
So 252771-08-7 is a valid CAS Registry Number.

252771-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ethynyl-2-hydroxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 5-ethynylsalicylaldehyde

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:252771-08-7 SDS

252771-08-7Relevant articles and documents

A Constrained and “Inverted” [3+3] Salphen Macrocycle with an ortho-Phenylethynyl Substitution Pattern

Torres, Tomas,Urbani, Maxence

, (2019)

A [3+3] Schiff-base salphen macrocycle (7 a) was synthesized by imine condensation between ortho-phenylenediamine and ortho-phenylethynyl-bridged bis(5-salicylaldehyde) precursors. The triangular-shaped macrocycle 7 a has a nonclassical (or “inverted”) de

Ru(III)-pseudohalide complexes with alkynyl functionalized salicylaldimine ligand and heterocyclic coligand: Synthesis, characterization, electrochemical and luminescence properties

Mohite,Patil-Deshmukh,Chavan

, (2020)

A new series of hexa-coordinated Ru(III) complexes of the type [Ru(L)(phen)X2] (1a-3a) and [Ru(L)(bipy)X2](1b-3b) [where, X = NCS, N3, CN] have been prepared by the reaction of RuCl3·H2O with 2-((E)-(4-(2-(4-methoxyphenyl)ethynyl)phenylimino)methyl)-4-(2-(4-methoxy phenyl)ethynyl)phenol (L) in presence of 1,10-phenanthroline (phen) or 2,2′-bipyridine (bipy) as a ligand. The molecular structure of ligand L was confirmed by single crystal X-ray diffraction. All complexes were characterized on the basis of elemental analysis, magnetic moment, TGA, IR, UV–Vis, EPR and mass spectral studies. The EPR spectral data and magnetic susceptibility measurement showed octahedral geometry around Ru(III). The electrochemical properties of all complexes indicate quasireversible redox behaviour corresponding to Ru(III)/Ru(IV) and Ru(III)/Ru(II) couple and are variable to π-acidic character of phen and bipy. All complexes exhibit strong emissions from lowest energy ILCT state with some LMCT character in DMF (10-4 M) at room temperature indicating that alkynyl functionality on salicylaldimine ligand enhances the emission property of the complexes and varies considerably with quenching ability of pseudohalides.

Ni(II) and Zn(II) Complexes Containing Alkynyl Functionalized Salicylaldimine Ligand and Heterocyclic Coligand: Synthesis, Characterization and Luminescence Properties

More,Devkule,Chavan

, p. 841 - 851 (2017)

Some nickel(II) and zinc(II) complexes of the type [Ni(L)(phen/bipy)]X (1a–6a) and [Zn(L) (phen/bipy)]X (1b–6b) (where L?=?2-{(E)-[(4-trimethylsilylethynylphenyl)imino]methyl}-4-(4-nitro phenylethynyl)phenol; phen?=?1, 10-phenanthroline, bipy?=?2, 2′-bipyridine; X?=?ClO4 ?, BF4 ?, PF6 ?) have been prepared and characterized on the basis of elemental analyses, FTIR, 1H NMR and mass spectral studies. The molecular structure of L was determined by single crystal X-ray diffraction studies. The electrochemical behaviour of the Ni(II) complexes indicate that the phen complexes appears at more positive potential as compared to those for bipy complexes, as a consequence of its strong π-acidic character. TGA was carried out to study the thermal behavior of the complexes. Room temperature luminescence is observed for all complexes corresponds to π?→?π* ILCT transition. The size of the counter anion and heterocyclic coligands phen and bipy shows marked effect on emission properties of the complexes.

Fluorescent probe, nerve agent detection element, preparation method and application

-

Paragraph 0068; 0070-0074, (2021/02/10)

The invention relates to the technical field of fluorescent probes, and particularly discloses a fluorescent probe, a nerve agent detection element, a preparation method and application. The structureof the fluorescent probe is shown as a formula 3. Accor

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