Welcome to LookChem.com Sign In|Join Free
  • or
4-(4-METHOXY-PHENYL)-2-METHYL-THIAZOLE is a chemical compound that belongs to the class of organic molecules known as thiazoles. Thiazoles are heterocyclic compounds with a five-member aromatic ring consisting of one sulfur atom, one nitrogen atom, and three carbon atoms. The 4-methoxy-phenyl group attached to the 4th carbon of the thiazole ring adds further structural complexity, while the methyl group on the 2nd carbon provides additional variation. 4-(4-METHOXY-PHENYL)-2-METHYL-THIAZOLE is often utilized in medicinal chemistry for drug discovery research.

50834-78-1

Post Buying Request

50834-78-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

50834-78-1 Usage

Uses

Used in Medicinal Chemistry:
4-(4-METHOXY-PHENYL)-2-METHYL-THIAZOLE is used as a compound in drug discovery research for its potential applications in the development of new pharmaceuticals. Its unique structural features may contribute to its interaction with biological targets, making it a valuable candidate for further investigation in the field of medicinal chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(4-METHOXY-PHENYL)-2-METHYL-THIAZOLE is used as a building block for the synthesis of various drug molecules. Its distinct chemical properties and structural characteristics may enable the creation of novel therapeutic agents with improved efficacy and reduced side effects.
Used in Chemical Research:
4-(4-METHOXY-PHENYL)-2-METHYL-THIAZOLE is also used as a research tool in chemical research to study the properties and reactivity of thiazoles and their derivatives. Understanding the behavior of 4-(4-METHOXY-PHENYL)-2-METHYL-THIAZOLE can provide insights into the design and synthesis of new molecules with potential applications in various fields, including materials science and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 50834-78-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,3 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50834-78:
(7*5)+(6*0)+(5*8)+(4*3)+(3*4)+(2*7)+(1*8)=121
121 % 10 = 1
So 50834-78-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NOS/c1-8-12-11(7-14-8)9-3-5-10(13-2)6-4-9/h3-7H,1-2H3

50834-78-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H66068)  4-(4-Methoxyphenyl)-2-methylthiazole, 97%   

  • 50834-78-1

  • 1g

  • 548.0CNY

  • Detail
  • Alfa Aesar

  • (H66068)  4-(4-Methoxyphenyl)-2-methylthiazole, 97%   

  • 50834-78-1

  • 5g

  • 2107.0CNY

  • Detail
  • Alfa Aesar

  • (H66068)  4-(4-Methoxyphenyl)-2-methylthiazole, 97%   

  • 50834-78-1

  • 25g

  • 8771.0CNY

  • Detail

50834-78-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-Methoxyphenyl)-2-methylthiazole

1.2 Other means of identification

Product number -
Other names 4-(4-methoxyphenyl)-2-methyl-1,3-thiazole

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:50834-78-1 SDS

50834-78-1Relevant academic research and scientific papers

Access to Thiazole via Copper-Catalyzed [3+1+1]-Type Condensation Reaction under Redox-Neutral Conditions

Tang, Xiaodong,Yang, Jidan,Zhu, Zhongzhi,Zheng, Meifang,Wu, Wanqing,Jiang, Huanfeng

, p. 11461 - 11466 (2016/11/28)

A new strategy for thiazoles via copper-catalyzed [3+1+1]-type condensation reaction from oximes, anhydrides and potassiumthiocyanate (KSCN) is developed herein. The transformation has good functional group tolerance and various thiazoles were formed smoothly in good to excellent yields under mild reaction conditions. This process involves copper-catalyzed N-O/C-S bond cleavages, activation of vinyl sp2 C-H bond, and C-S/C-N bond formations which are under redox-neutral conditions as well as operational simplicity.

Exploration and Optimization of an Efficient One-pot Sequential Synthesis of Di/tri-substituted Thiazoles from α-Bromoketones, Thioacids Salt, and Ammonium Acetate

Venkateswararao, Eeda,Jalani, Hitesh B.,Manoj,, Manickam,Jung, Sang-Hun

, p. 1449 - 1456 (2016/09/24)

Exploration of scope of an optimized one-pot sequential procedure for preparing of 2,4-di- and 2,4,5-tri-substituted thiazoles has been accomplished. The synthesis was performed by the initial formation of a β-keto-thioester intermediate from nucleophilic substitution of α-bromoketones with thioacid potassium salts, followed by treatment with ammonium acetate and one equivalent of acetic acid in toluene to form imine intermediate eventually leading to cyclization yielding thiazoles. This procedure should be highlighted with a flexible way to control the substitution pattern around thiazole ring by choosing appropriately substituted α-bromoketones even containing acid labile functionality and thioacid potassium salts, and thus its applicability is very wide.

Lipase and deep eutectic mixture catalyzed efficient synthesis of thiazoles in water at room temperature

Lobo, Hyacintha Rennet,Singh, Balvant Shyam,Shankarling, Ganapati Subray

, p. 1369 - 1375 (2013/01/15)

Lipase bio-catalyst or ammonium based deep eutectic mixture efficiently catalyzed aqueous phase synthesis of methyl-thiazole and amino-thiazole derivatives. The simple ammonium deep eutectic catalyst, easily synthesized from choline chloride and urea, is inexpensive, recyclable and bio-degradable, making it suitable for industrial applications. Springer Science+Business Media, LLC 2012.

Efficient synthesis of 2,4-disubstituted thiazoles under grinding

Heravi, Majid M.,Poormohammad, Nargess,Beheshtiha, Yahia S.,Baghernejad, Bita

experimental part, p. 579 - 582 (2011/04/22)

A simple and convenient protocol is described for the preparation of 2,4-disubstituted thiazoles via a condensation reaction of -halo carbonyl compounds with thiourea or thioacetamide at room temperature, under grinding, in good yields.

Synthesis, characterization, and antimicrobial evaluation of oxadiazole congeners

Sadek, Bassem,Fahelelbom, Khairi Mustafa Salem

experimental part, p. 4339 - 4347 (2011/08/10)

A series of 1,3-oxazole, 1,3-thiazole, isomeric 1,2,4-oxadiazole, 1,3,4-oxadiazole, and 1,2,3,4-tetrazole heterocycles was synthesized. All the compounds shared as a common feature the presence of a 4-hydroxyphenyl substituent. The structures of the synthesized compounds were confirmed by MS, 1H-NMR, and elemental analysis. In vitro antimicrobial activity for all the newly synthesized compounds at concentrations of 200-25 μg/mL was evaluated against Gram+ve organisms such as methicillin-resistant Staphylococcus aureus (MRSA), Gram-ve organisms such as Escherichia coli (E. coli), and the fungal strain Aspergillus niger (A. niger) by the cup plate method. Ofloxacin and ketoconazole (10 μg/mL) were used as reference standards for antibacterial and antifungal activity, respectively. Compounds 15, 16, and 20 showed notable antibacterial and antifungal activities at higher concentrations (200 μg/mL), whereas 17-19 were found to display significant antibacterial or antifungal activity (25-50 μg/mL) against the Gram+ve, Gram-ve bacteria, or fungal cells used in the present study.

Novel bisaryl substituted thiazoles and oxazoles as highly potent and selective peroxisome proliferator-activated receptor δ agonists

Epple, Robert,Cow, Christopher,Xie, Yongping,Azimioara, Mihai,Russo, Ross,Wang, Xing,Wityak, John,Karanewsky, Donald S.,Tuntland, Tove,Nguyê?-Tran, Van T. B.,Ngo, Cara Cuc,Huang, David,Saez, Enrique,Spalding, Tracy,Gerken, Andrea,Iskandar, Maya,Seidel, H. Martin,Tian, Shin-Shay

experimental part, p. 77 - 105 (2010/04/30)

The discovery, synthesis, and optimization of compound 1 from a high-throughput screening hit to highly potent and selective peroxisome proliferator-activated receptor δ (PPARδ) agonists are reported. The synthesis and structure-activity relationship in this series are described in detail. On the basis of a general schematic PPAR pharmacophore model, scaffold 1 was divided into headgroup, linker, and tailgroup and successively optimized for PPAR activation using in vitro PPAR transactivation assays. A (2-methylphenoxy)acetic acid headgroup, a flexible linker, and a five-membered heteroaromatic center ring with two hydrophobic aryl substituents were required for efficient and selective PPARδ activation. The fine-tuning of these aryl substituents led to an array of highly potent and selective compounds such as compound 38c, displaying an excellent pharmacokinetic profile in mouse. In an in vivo acute dosing model, selected members of this array were shown to induce the expression of pyruvate dehydrogenase kinase-4 (PDK4) and uncoupling protein-3 (UCP3), genes that are known to be involved in energy homeostasis and regulated by PPARδ in skeletal muscle.

A rapid and high-yielding synthesis of thiazoles and aminothiazoles using tetrabutylammonium salts

Kocabas, Erdal,Sariguney, Ahmet Burak,Coskun, Ahmet

experimental part, p. 2849 - 2854 (2011/04/16)

A convenient method for the synthesis of thiazoles and aminothiazoles by treatment of phenacyl bromides with thioamides/thiourea in the presence of tetrabutylammonium hexafluorophosphate (Bu4NPF6) at room temperature was developed. The products having high yields were formed rapidly (within 15 min). The method is simple, rapid and practical, generating thiazole derivatives in excellent isolated yields. The structures of the newly synthesized products were identified by FT-IR, 1H NMR, 13C NMR spectroscopy and elemental analysis data. The Japan Institute of Heterocyclic Chemistry.

Efficient and expeditious synthesis of di- and trisubstituted thiazoles in PEG under catalyst-free conditions

Zhu, Dongjian,Chen, Jiuxi,Xiao, Huilong,Liu, Miaochang,Ding, Jinchang,Wu, Huayue

experimental part, p. 2895 - 2906 (2009/12/03)

An efficient and expeditious catalyst-free protocol was developed for the construction of di- and trisubstituted thiazoles from -haloketones and thioureas/thioamides in PEG. The reaction was carried out at ambient temperature, and the products were obtained in excellent isolated yields (91-98%). Additionally, PEG could be recovered easily and was reused without evident loss in activity.

An efficient, catalyst- and solvent-free synthesis of imidazo[1,2-a] pyridines and 2,4-disubstituted thiazoles on grinding

Zhu, Dongjian,Chen, Jiuxi,Wu, Dengze,Liu, Miaochang,Ding, Jinchang,Wu, Huayue

experimental part, p. 84 - 86 (2009/10/15)

An efficient synthesis of imidazo[1,2-a]pyridines and 2,4-disubstituted thiazoles in excellent yield under catalyst-and solvent-free conditions at room temperature on grinding has been developed. The important features of this method are that it is reasonably fast, very clean, high yielding, simple workup and environmentally benign.

Liquid-phase organic synthesis of thiazoles using poly(ethylene glycol)-bound sulfonyl chloride resin

Liu, Xiao-Ling,Wang, Qiu-Ying,Sheng, Shou-Ri,Xu, Chen,Cai, Ming-Zhong

, p. 3338 - 3345 (2008/12/22)

Reaction of poly(ethylene glycol) (PEG)-bound sulfonic acid with thionyl chloride formed difunctionalized PEG-bound sulfonyl chloride, which was treated with α-hydroxyketones, followed by treatment with thioamides in the presence of potassium carbonate, to afford thiazoles in good yields with a facile workup procedure. Copyright Taylor & Francis Group, LLC.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 50834-78-1