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"6-{[(3-acetylphenyl)amino]methylidene}cyclohexa-2,4-dien-1-one" is a complex organic compound characterized by a cyclohexa-2,4-dien-1-one core, which features a conjugated diene system. The molecule is further defined by the presence of a 3-acetylphenyl group, which is attached to the cyclohexadienone ring through an aminomethylene bridge. The acetyl group in this context is an acetate derivative, indicating the presence of a carbonyl group bonded to a methyl group. 6-{[(3-acetylphenyl)amino]methylidene}cyclohexa-2,4-dien-1-one is likely to be involved in chemical reactions due to its reactive functional groups, such as the carbonyl and the diene system, and may have applications in the synthesis of pharmaceuticals or other organic compounds.

788-18-1

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788-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 788-18-1 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 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 788-18:
(5*7)+(4*8)+(3*8)+(2*1)+(1*8)=101
101 % 10 = 1
So 788-18-1 is a valid CAS Registry Number.

788-18-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (6E)-6-[(3-acetylanilino)methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names N-3-acetophenylsalicylaldimine

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:788-18-1 SDS

788-18-1Relevant academic research and scientific papers

Polymorphism control in the mechanochemical and solution-based synthesis of a thermochromic Schiff base

Zba?nik, Marija,Nogalo, Ivana,Cin?i?, Dominik,Kaitner, Branko

, p. 7870 - 7877 (2015)

Three crystal forms of a thermochromic Schiff base, namely 1-{3-[(2-hydroxy-3-methoxy-benzylidene)-amino]-phenyl}-ethanone, derived from o-vanillin and 3-aminoacetophenone, were obtained by conventional solution-based methods. Two out of the three polymorphs were synthesized by mechanochemical syntheses, under solvent-free conditions. Herein, we report a study of the dependence of the composition of solvent, the crystallization temperature and impurities on the outcome of the synthesis of Schiff base polymorphs. We report the important role of seed crystals in directing the supramolecular organization of the product of a covalent solvent-free reaction towards the intended polymorphic outcome as well. All obtained polymorphs were investigated by means of thermal analysis, single crystal X-ray diffraction, ex situ and in situ powder X-ray diffraction and IR spectroscopy. The polymorphs display interesting and remarkably different molecular packing arrangements governed by C-H?O interactions leading to two-dimensional networks in forms I and III, and a three-dimensional networks in form II.

Antiobesity, antioxidant and cytotoxicity activities of newly synthesized chalcone derivatives and their metal complexes Dedicated to Professor R. R. Schmidt on the occasion of his 79th birthday.

El Sayed Aly, Mohamed Ramadan,Abd El Razek Fodah, Hamadah Hamadah,Saleh, Sherif Yousef

, p. 517 - 530 (2014/03/21)

Four sets of rationally designed chalcones were prepared for evaluation of their antiobesity, antioxidant and cytotoxicity activities. These sets include nine oleoyl chalcones as mimics of oleoyl estrone, three monohydroxy chalcones (chalcone ligands), Schiff base-derived chalcones and four copper as well as zinc complexes. Oleoyl chalcones 4d, 4e and particularly 6a as an isosteric isomer of oleoyl estrone, were as active as Orlistat on weight loss and related metabolic parameters using male SD rats in vivo. Chalcone ligands 10a-c and Schiff base-derived chalcones 11 and 14a,b were weakly antioxidants, while, the copper and zinc complexes 15a-d were good antioxidants with zinc chelates 15b,d being more active than their copper analogues 15a,cin vitro. Compounds 10c and 14a showed good cytotoxicity activities as Doxorubicin against PC3 cancer cell line in vitro, while, the copper complex 15c showed promising activity with IC50 value of 5.95 μM. The estimated IC50 value for Doxorubicin was 8.7 μM. Chalcones 14a,b are bifunctional probes for potential investigations in cancer diagnosis and radiotherapy by complexation with Gd3+ or metal radioisotopes followed by posttranslation of Shiga toxin B-subunits that target globotriosyl ceramide expressing cancer cells.

Design, synthesis and in vitro antimalarial evaluation of new quinolinylhydrazone derivatives

Thuy, Le Thi,Tien, Hoang Xuan,Hoang, Vu Dinh,Vu, Tran Khac

scheme or table, p. 163 - 168 (2012/07/17)

A series of novel quinolinylhydrazones (5a-f) was synthesized by the condensation reaction of 2,6-diaryl-substituted piperidin-4-ones (4a-f) with 7-chloro-4-hydrazinoquinoline (2). Novel quinolinylhydrazones containing Shiff bases 8a-f and 11a-f were obta

The synthesis and structure of l-[3-{(2-hydroxybenzylidene)amino}phenyl] ethanone

De Lai, Rajib,Mukhcrjee, Jaydcep,Mandal, Mahuya,Roy, Lovely,Bhowal, Ruchika,Banerjee, Indrajit

experimental part, p. 595 - 598 (2009/12/24)

Two Schiff base Iigands SACPNyH 1 and 5BrSACPNyH 2 are synthesized from the condensation reactions of salicylaldehyde and 5-bromosalicyIaldehyde respectively with 3-aminoaceto- phenone and characterized by elemental analyses, mass, electronic, infrared sp

Solvent-free syntheses of salicylaldimines assisted by microwave irradiation

Yang, Haijian,Sun, Wen-Hua,Li, Zilong,Wang, Leyong

, p. 2395 - 2402 (2007/10/03)

A microwave-assisted condensation of salicylaldehyde and aryl amines without solvent were efficiently performed to form a series of salicylaldimines in high yields, which were confirmed by IR, 1H NMR, 13C NMR and elemental analyses. The microwave-assisted condensation provided a convenient environmental-friendship methodology for syntheses of Schiff-base in organic syntheses.

Mixed ligand complexes of cobalt(II and III) - Molecular structure of bis-(4-acetophenylsalicylaldiminato)acetylacetonato cobalt(III)

De Lal,Banerjee,Mukherjee,Guha

, p. 1050 - 1054 (2007/10/03)

The bidentate Schiff bases, HL′(= N-4-acetophenylsalicylal-dimine), H″(=N-3-acetophenylsalicylaldimine) and HL? (=N-4-acetophenyl-5-bromosalicylaldimine) do not form complexes with simple cobalt(II)salts, e.g.,Co(CH3COO)2.4H2/s

Exchange of amine part of schiff bases with ammonia in presence of a metal ion: Molecular structure of bis-(salicylaldiminato) nickel(II)

De, Rajib Lal,Banerjee, Indrajit,Samanta, Chitra,Mukherjee, Alok K.

, p. 373 - 376 (2007/10/03)

The schiff bases N-X1-acetophenyl-X2-salicylaldimines (X1=4 or 3; *X2=H or 5Br) inert to complexation with nickel(II) and cobalt(II) salts undergo very prompt reactions when ammonia is added to the reaction mixt

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