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782-76-3

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782-76-3 Usage

General Description

2-{[(4-methylphenyl)imino]methyl}phenol is a chemical compound with a molecular formula C14H13NO. It is a derivative of phenol and is known for its antioxidant and antimicrobial properties. The compound is often used in the manufacture of pharmaceuticals and can also be found in some personal care products. It has been studied for its potential use in the treatment of various conditions, including cancer and inflammatory diseases. Additionally, it has been shown to have potential as a corrosion inhibitor, making it useful in industrial applications. Overall, 2-{[(4-methylphenyl)imino]methyl}phenol is a versatile compound with various potential uses in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 782-76-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 782-76:
(5*7)+(4*8)+(3*2)+(2*7)+(1*6)=93
93 % 10 = 3
So 782-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO/c1-11-6-8-13(9-7-11)15-10-12-4-2-3-5-14(12)16/h2-10,15H,1H3

782-76-3SDS

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 6-[(4-methylanilino)methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names N-Salicylidene-p-toluidine

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:782-76-3 SDS

782-76-3Relevant articles and documents

Synthesis, structural characterization, and catalytic activity of ruthenium(II) monocarbonyl complexes with bidentate Schiff base and triphenylphosphine ligands

Yin, Xiao-Feng,Lin, Hui,Jia, Ai-Quan,Chen, Qun,Zhang, Qian-Feng

, p. 3229 - 3240 (2013)

Treatment of [RuHCl(CO)(PPh3)3] with equal amounts of equiv bidentate Schiff base 2[(4-chloro-phenylimino)-methyl]-phenol (HL-Cl) or 2(p-tolylimino-methyl)-phenol (HL-Me) or 2[(4-nitro-phenylimino)-methyl]-phenol (HL-NO2) in the presence of triethylamine afforded [RuCl(2-N,O-L-Cl) (CO)(PPh3)2] (1), [RuCl(2-N,O-L-Me)(CO)(PPh3)2] (2), and [RuCl( 2-N,O-L-NO2)(CO)(PPh3)2] (3), respectively The molecular structures of 1, 2, and 3·1.5C6H14 have been determined by single-crystal X-ray crystallography Complexes 1-3 were used for oxidation of primary and secondary alcohols to aldehydes and ketones as catalysts in the presence of N-methylmorpholine-N-oxide 2013

Synthesis, characterization and anti-cancer studies of Mn(II), Cu(II), Zn(II) and Pt(II) dithiocarbamate complexes - crystal structures of the Cu(II) and Pt(II) complexes

Ajibade, Peter A.,Fatokun, Amos A.,Andrew, Fartisincha P.

, (2020/01/23)

Mn(II), Cu(II), Zn(II) and Pt(II) complexes of 2-((p-tolylamino)methyl)phenolyldithiocarbamate were synthesized and characterized by elemental analyses and spectroscopic techniques. Spectroscopic studies indicate four coordinate geometry around the metal(

Synthesis of novel Schiff bases using green chemistry techniques; antimicrobial, antioxidant, antiurease activity screening and molecular docking studies

Mermer, Arif,Demirbas, Neslihan,Uslu, Harun,Demirbas, Ahmet,Ceylan, Sule,Sirin, Yakup

, p. 412 - 422 (2019/01/21)

Schiff base derivatives were synthesized in this study via conventional, microwave irradiation and ultrasound sonication methods. Optimization conditions were examined for several parameter such as solvent, reaction time and yield. After determining the o

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