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1-[(1-Naphthylimino)methyl]-2-naphthol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29101-37-9

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29101-37-9 Usage

Type of compound

Naphthol derivative

Functional group

Imine group

Application

Coordination chemistry as a ligand

Potential pharmaceutical applications

Anti-inflammatory and antimicrobial properties

Antioxidant activity

Strong

Investigated for treatment of

Cancer and neurodegenerative disorders

Utilized as

Fluorescent dye in biological imaging

Utilized as

Reagent in organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 29101-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,0 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29101-37:
(7*2)+(6*9)+(5*1)+(4*0)+(3*1)+(2*3)+(1*7)=89
89 % 10 = 9
So 29101-37-9 is a valid CAS Registry Number.

29101-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-Naphthylcarbonoimidoyl)-2-naphthol

1.2 Other means of identification

Product number -
Other names 3-hydroxy-2,7-naphthalenedicarboxylic acid

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:29101-37-9 SDS

29101-37-9Downstream Products

29101-37-9Relevant academic research and scientific papers

Palladium(II) complexes comprising naphthylamine and biphenylamine based Schiff base ligands: Synthesis, structure and catalytic activity in Suzuki coupling reactions

Balasubramani, Kasturi,Kaleeswaran, Dhananjayan,Nagalakshmi, Veerasamy,Premkumar, Muniyappan,Sathya, Munusamy,Venkatachalam, Galmari

, (2020/03/18)

New palladium(II) Schiff base complexes of the general formula [Pd(L1?6)2] [L1 = N-(Naphthyl)-salicylaldimine (1), L2 = N-(Naphthyl)-methoxysalicylaldimine (2), L3 = N-(Biphenyl)-salicylaldimine (3), L4 = N-(Biphenyl)-methoxysalicylaldimine (4), L5 = N-(Naphthyl)-2-hydroxy-1-naphthaldimine (5), L6 = N-(Biphenyl)-2-hydroxy-1-naphthaldimine (6)] 1–6 have been synthesized by the reaction of [Pd(OAc)2] with bidentate Schiff base ligands. The palladium(II) complexes were fully characterized by analytical, spectral (FT?IR, UV–Vis, 1H NMR & 13C NMR) methods. The molecular structure of the one of the complexes [Pd(L1)2] (6) was confirmed by single crystal X?ray diffraction methods. Further, the new palladium(II) complexes were tested as catalyst for Suzuki-Miyaura coupling reactions and exhibits very good catalytic activity.

Palladium(0)-mediated C-H bond activation of N-(naphthyl)salicylaldimine and related ligands: utilization of the resulting organopalladium complexes in catalytic C-C and C-N coupling reactions

Dutta, Jayita,Richmond, Michael G.,Bhattacharya, Samaresh

, p. 13615 - 13632 (2015/08/03)

N-(Naphthyl)-4-R-salicylaldimines (R = OCH3, H and Cl; H2L1-H2L3) and 2-hydroxy-N-(naphthyl)naphthaldimine (H2L4) readily undergo, upon reaction with Na2[PdCl4] in the presence of triphenylphosphine, cyclopalladation via C-H bond activation at the peri-position to afford complexes of type [Pd(L)(PPh3)] (L = L1-L4). The C-H bond activation has been found to be mediated by palladium(0) formed in situ. A similar reaction of H2L1 with Na2[PdCl4] in the presence of 1,2-bis(diphenylphosphino)ethane (dppe), in a 2 : 2 : 1 mole ratio, yields a dinuclear complex of type [{Pd(L1)}2(dppe)]. Reaction of H2L1 with Na2[PdCl4] in the presence of 4-picoline (pic) yields [Pd(L1)(pic)]. The molecular structures of the six complexes have been determined by X-ray crystallography. The aldiminate ligand in each compound is coordinated to the metal center as a di-anionic tridentate ONC-donor, with the fourth coordination site occupied by a phosphine or picoline ligand. The new complexes show intense absorptions in the visible and ultraviolet regions, and the nature of the optical transitions has been analyzed by TDDFT calculations. The palladium complexes display notable efficiency in catalyzing C-C and C-N bond coupling reactions. The thermodynamics for the formation of the cyclometalated catalyst precursor [Pd(L2)(PPh3)] has been evaluated by DFT calculations.

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