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3-[(4-phenyl-1,3-thiazol-2-yl)amino]phenol is a complex organic compound with the molecular formula C15H11NOS2. It features a phenol group (C6H5OH) connected to a 1,3-thiazole ring, which in turn is linked to an aniline group (C6H5NH2). The thiazole ring is substituted with a phenyl group at the 4-position, and the aniline group is attached to the 3-position of the phenol. 3-[(4-phenyl-1,3-thiazol-2-yl)amino]phenol is known for its potential applications in the synthesis of pharmaceuticals and other chemical industries due to its unique structure and reactivity. It is important to note that handling and use of this chemical should be done with caution, as it may have specific safety and health considerations.

3394-27-2

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3394-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3394-27-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,9 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3394-27:
(6*3)+(5*3)+(4*9)+(3*4)+(2*2)+(1*7)=92
92 % 10 = 2
So 3394-27-2 is a valid CAS Registry Number.

3394-27-2Downstream Products

3394-27-2Relevant academic research and scientific papers

Thiocyanation and 2-Amino-1,3-thiazole Formation in Water Using Recoverable and Reusable Glycosylated Resorcin[4]arene Cavitands

Husain, Ali A.,Bisht, Kirpal S.

, p. 9928 - 9935 (2020/09/03)

A family of three spatially directional resorcin[4]arene cavitand glycoconjugates (RCGs) have been applied as efficient recoverable and reusable inverse phase transfer catalysts for eco- A nd environmentally friendly thiocyanation and 2-amino-1,3-thiazole formation reactions in water. The results show that RCGs (1 mol %) were capable of hosting and catalyzing various water-insoluble bromo/thiocyanato substrates in water without the use of any co-organic solvents. The recoverability and reusability of RCG catalytic systems, that is, RCG1 and RCG3, were also examined upon a simple extraction of the desired products using DCM or ethyl acetate, followed by subjecting the recovered aqueous solution containing the RCG catalysts to the next reaction cycles.

A library of novel allosteric inhibitors against fructose 1,6-bisphosphatase

Heng, Sabrina,Gryncel, Kimberly R.,Kantrowitz, Evan R.

experimental part, p. 3916 - 3922 (2009/10/02)

The identification of a proper lead compound for fructose 1,6-bisphosphatase (FBPase) is a critical step in the process of developing novel therapeutics against type-2 diabetes. Herein, we have successfully generated a library of allosteric inhibitors against FBPase as potential anti-diabetic drugs, of which, the lead compound 1b was identified through utilizing a virtual high-throughput screening (vHTS) system, which we have developed. The thiazole-based core structure was synthesized via the condensation of α-bromo-ketones with thioureas and substituents on the two aryl rings were varied. 4c was found to inhibit pig kidney FBPase approximately fivefold better than 1b. In addition, we have also identified 10b, a tight binding fragment, which can be use for fragment-based drug design purposes.

METHODS OF USING THIAZOLE, OXAZOLE AND IMIDAZOLE COMPOUNDS IN TREATING SODIUM CHANNEL-MEDIATED DISEASES OR CONDITIONS

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Page/Page column 95; 96, (2008/12/08)

This invention is directed to methods of using thiazole, oxazole and imidazole compounds of formula (I): wherein A is -S-, -O- or N(R5), and R1, R2, R3 and R5 are as defined herein, as a stereoisomer, enantiomer, tautomer thereof or mixtures thereof; or a pharmaceutically acceptable salt, solvate or prodrug thereof, for the treatment and/or prevention of sodium channel-mediated diseases or conditions, such as pain.

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