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N-(5-methyl-2-thienylmethylidene)-o-aminophenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99303-11-4

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99303-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99303-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,0 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99303-11:
(7*9)+(6*9)+(5*3)+(4*0)+(3*3)+(2*1)+(1*1)=144
144 % 10 = 4
So 99303-11-4 is a valid CAS Registry Number.

99303-11-4Downstream Products

99303-11-4Relevant academic research and scientific papers

Palladium(II) complexes of N-(2-thienylmethylidene)aniline derivatives

Hwang, Wen-Shu

, p. 529 - 533 (1999)

Coordination reactions of N-(2-thienylmethylidene)aniline derivatives, L, with PdCl2 or [PdCl4]2- in ethanol yield stable complexes of the type trans-(L)2PdCl2 with the azomethine nitrogen atoms as σ

Vanadium(III) complexes containing phenoxy–imine–thiophene ligands: Synthesis, characterization and application to homo- and copolymerization of ethylene

do Prado, Nayara T.,Ribeiro, Ronny R.,L. Casagrande, Osvaldo

, (2017)

A set of vanadium(III) complexes, namely {SNO}VCl2(THF)2 (2a, SNO?=?thiophene-(N═CH)-phenol; 2b, SNO?=?5-phenylthiophene-(N═CH)-phenol; 2c, SNO?=?5-phenylthiophene-(N═CH)-4-tert-butylphenol; 2d, SNO?=?5-methylthiophene-(N═CH)-phenol;

Iodine (III)-mediated synthesis of some 2-aryl/ hetarylbenzoxazoles as antibacterial/antifungal agents

Kumar, Ravi,Nair, Reshmi R.,Dhiman, Saurabh Sudha,Sharma, Jitender,Prakash, Om

experimental part, p. 541 - 550 (2011/11/01)

Ten 2-aryl/hetarylbenzoxazoles (5a, 5b, and 6a-h) were synthesized via oxidative cyclization of Schiff bases (3a, 3b, and 4a-h) with 1.1 equivalent of iodobenzene diacetate (IBD) in methanol. All of these 2-aryl/hetarylbenzoxazoles (5a, 5b, and 6a-h) were tested in vitro for their antibacterial and antifungal activities against Bacillus subtilis, Bacillus stearothermophilus, Escherichia coli, and Pseudomonas putida. These compounds also were screened for their antifungal activity against Aspergillus flavus and Aspergillus niger. Biological activity of these compounds was compared with those of commercially available antibiotics, chloramphenicol and antifungal agent cycloheximide. Most of these compounds, 5a, 5b, 6a, 6b, 6d, 6e, 6g, 6h, were equipotent or more potent than these commercial drugs at concentration 100 μg/ml. Birkhaeuser Boston 2009.

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