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Phenol, 4-bromo-2-[[[2-(2-pyridinyl)ethyl]imino]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112359-98-5

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112359-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112359-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,5 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112359-98:
(8*1)+(7*1)+(6*2)+(5*3)+(4*5)+(3*9)+(2*9)+(1*8)=115
115 % 10 = 5
So 112359-98-5 is a valid CAS Registry Number.

112359-98-5SDS

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-bromo-6-[(2-pyridin-2-ylethylamino)methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names N-(pyridine-2-ylethyl)-2-hydroxy-5-bromo-benzylideneamine

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:112359-98-5 SDS

112359-98-5Downstream Products

112359-98-5Relevant academic research and scientific papers

Single-Molecule-Magnet FeII4FeIII2 and Antiferromagnetic FeIII4 Coordination Clusters

Barman, Suman K.,Cano, Joan,Lloret, Francesc,Mukherjee, Rabindranath

, p. 8086 - 8099 (2019)

Supported by endogenous (part of the ligand, in-built) phenoxo bridges provided by the ligand 2,6-bis[{{(5-bromo-2-hydroxybenzyl)}{(2-(pyridylethyl)}amino}methyl]-4-methylphenol) (H3L), in its deprotonated form, exogenous (not part of the ligan

Catalysis of alkene epoxidation by manganese(II) and (III) complexes of both Schiff base and reduced Schiff base ligands utilizing environmentally benign H2O2

Egekenze, Rita,Gultneh, Yilma,Butcher, Ray

, p. 198 - 209 (2018)

Mono and disubstituted tridentate Schiff base ligands were synthesized from the reaction of 2(2-aminoethyl)pyridine with 5-bromosalicylaldehyde (H-L1) and 3,5-dibromosalicylaldehyde (H-L2) respectively, which were subsequently reacte

Cytotoxic oxidovanadium(IV) complexes of tridentate halogen‐substituted Schiff bases: First dinuclear V(IV) complexes with O → VIV = O → VIV = O core

Aryaeifar, Mahnaz,Blacque, Olivier,Correia, Isabel,Marques, Fernanda,Micale, Nicola,Rudbari, Hadi Amiri,Saadati, Arezoo

supporting information, (2021/08/16)

The reaction of potentially N,N,O-tridentate Schiff base ligands, Cl-LH, Br-LH, BrCl-LH and H-LH, with [VIVO(acac)2] in 2:1 ratio in methanol gave the corresponding mononuclear and dinuclear oxidovanadium(IV) complexes, VO(Cl-L)

Synthesis, characterization, and formation constant of hexacoordinate iron(III) complexes

Asadi, Mozaffar,Hemmateenejad, Bahram,Mohammadikish, Maryam

experimental part, p. 124 - 135 (2010/09/10)

Twelve iron(III) complexes [FeIII(LX)2]ClO4, where (LX)- is the deprotonated form of a series of asymmetric ligands containing pyridine and substituted phenol moieties (XPh(OH)-CH=N-(CH2)n-Py that X = H, 5-Br, 5-NO2, 5-OMe, 4-OMe, 3-OMe, and n = 1, 2), were synthesized and characterized by H NMR, IR, UV-Vis spectroscopy, mass spectrometry, and elemental analysis. Formation constants were measured using UV-Vis spectrophotometric titration at constant ionic strength (0.10 M NaClO4) at 25 (±0.1)°C. The trend of the complex formation of Fe(III) ion with a given tridentate ligand decreases as follows: 5-OMe > 5-H > 5-NO2 > 5-Br 5-OMe > 4-OMe > 5-OMe.

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