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5-(4-methylphenyl)-2-phenylthiazole is an organic compound characterized by a thiazole ring, which is a five-membered heterocyclic structure containing a sulfur atom and a nitrogen atom. The molecule features a 4-methylphenyl group attached to the thiazole ring at the 5-position and a phenyl group at the 2-position. This chemical is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique structure and properties. It is synthesized through chemical reactions and can be used as a building block for more complex molecules or as a compound with specific biological activities.

6071-54-1

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6071-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6071-54-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6071-54:
(6*6)+(5*0)+(4*7)+(3*1)+(2*5)+(1*4)=81
81 % 10 = 1
So 6071-54-1 is a valid CAS Registry Number.

6071-54-1Relevant academic research and scientific papers

Cu-Catalyzed Aerobic Oxidative Sulfuration/Annulation Approach to Thiazoles via Multiple Csp3-H Bond Cleavage

Wang, Xiaoyang,Qiu, Xu,Wei, Jialiang,Liu, Jianzhong,Song, Song,Wang, Wen,Jiao, Ning

supporting information, p. 2632 - 2636 (2018/05/22)

A novel and practical Cu-catalyzed aerobic oxidative synthesis of thiazoles was developed. This chemistry for the first time achieved thiazole construction from simple aldehydes, amines, and element sulfur through multiple Csp3-H bond cleavage processes. Molecular oxygen was used as a green oxidant in this oxidative protocol. The substrate scope is broad with the tolerance of aliphatic amines. The mechanistic study might promote the reaction design for a new sulfuration/annulation reaction with readily available element sulfur.

Facile Synthesis of 2,5-Disubstituted Thiazoles from Terminal Alkynes, Sulfonyl Azides, and Thionoesters

Miura, Tomoya,Funakoshi, Yuuta,Fujimoto, Yoshikazu,Nakahashi, Junki,Murakami, Masahiro

, p. 2454 - 2457 (2015/05/27)

A sequential procedure for the synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters is reported. A copper(I)-catalyzed 1,3-dipolar cycloaddition of terminal alkynes with sulfonyl azides affords 1-sulfonyl-1,2,3-triazoles, which then react with thionoesters in the presence of a rhodium(II) catalyst. The resulting 3-sulfonyl-4-thiazolines subsequently aromatize into the corresponding 2,5-disubstituted thiazoles by elimination of the sulfonyl group. (Chemical Equation Presented).

Pd nanoparticle-silica nanotubes (Pd@SNTs) as an efficient catalyst for Suzuki-Miyaura coupling and sp2 C-H arylation in water

Park, Ginam,Lee, Sanghee,Son, Sang Jun,Shin, Seunghoon

supporting information, p. 3468 - 3473 (2013/12/04)

Silica nanotubes (SNTs) functionalized with Pd-NPs on the inner surface performed as efficient nano-reactors for C-C coupling in water; the nano-confinement offers minimized leaching of Pd and yet efficient mass transfer for Suzuki-Miyaura coupling and C-H arylation of thiazoles in water with very high TON.

Programmed synthesis of arylthiazoles through sequential C-H couplings

Tani, Satoshi,Uehara, Takahiro N.,Yamaguchi, Junichiro,Itami, Kenichiro

, p. 123 - 135 (2014/01/06)

A programmed synthesis of privileged arylthiazoles via sequential C-H couplings catalyzed by palladium or nickel catalysts has been accomplished. This versatile protocol can supply all possible arylthiazole substitution patterns (2-aryl, 4-aryl, 5-aryl, 2

Oxidative biaryl coupling of thiophenes and thiazoles with arylboronic acids through palladium catalysis: Otherwise difficult C4-selective C-H arylation enabled by boronic acids

Kirchberg, Sylvia,Tani, Satoshi,Ueda, Kirika,Yamaguchi, Junichiro,Studer, Armido,Itami, Kenichiro

, p. 2387 - 2391 (2011/04/21)

(Chemical Equation Presented) It adds up to 4! Thiophenes and thiazoles can be arylated in the 4- rather than the expected 5-position in a new C-H functionalization reaction (see scheme; TEMPO: 2,2,6,6-tetramethylpiperidine-N- oxyl). The boronic acid proved to be the key to achieving the otherwise difficult C4 selectivity. The method was applied to a concise synthesis of a key pharmacological structure with potential for treatment of Alzheimers disease.

Direct arylation of thiazoles on water

Turner, Gemma L.,Morris, James A.,Greaney, Michael F.

, p. 7996 - 8000 (2008/09/17)

Wetter is better: The direct arylation of thiazoles on water is quicker, cleaner, and higher-yielding than arylation in organic solvents. The reaction works under mild conditions for an array of aryl iodides, producing 2,5-diaryl thiazoles in excellent yields. Importantly, novel bi-heteroaryl compounds are produced without the requirement for stoichiometric organometallic coupling agents. (Figure Presented).

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