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1-(2-PHENYL-1,3-THIAZOL-5-YL)-1-ETHANONE is a chemical compound that belongs to the class of organic compounds known as thiazoles. These are heterocyclic compounds characterized by a five-member aromatic ring composed of one sulfur atom, one nitrogen atom, and three carbon atoms. The molecular formula of 1-(2-PHENYL-1,3-THIAZOL-5-YL)-1-ETHANONE is C11H9NOS, and it has a molecular weight of 203.26 g/mol. As an organic compound, it can be utilized in various scientific and industrial applications, although specific uses, safety, toxicity, and environmental impact information may require further research.

10045-50-8

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10045-50-8 Usage

Uses

1-(2-PHENYL-1,3-THIAZOL-5-YL)-1-ETHANONE is used as a chemical intermediate in the synthesis of various compounds for different industries. Its presence in the thiazoles class suggests potential applications in pharmaceuticals, agrochemicals, and materials science due to the diverse properties and reactivity of thiazoles.
Used in Pharmaceutical Industry:
1-(2-PHENYL-1,3-THIAZOL-5-YL)-1-ETHANONE is used as a building block for the development of new pharmaceutical compounds, given the versatility of the thiazole ring in medicinal chemistry. It can be incorporated into drug molecules to impart specific biological activities or improve pharmacokinetic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(2-PHENYL-1,3-THIAZOL-5-YL)-1-ETHANONE may serve as a precursor for the synthesis of pesticides or other agrochemical products, where the thiazole structure could contribute to the desired biological activity against pests or diseases.
Used in Materials Science:
1-(2-PHENYL-1,3-THIAZOL-5-YL)-1-ETHANONE could be utilized in the development of new materials with unique properties, such as in the synthesis of dyes, pigments, or polymers where the thiazole ring might enhance stability, color, or other characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 10045-50-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,4 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10045-50:
(7*1)+(6*0)+(5*0)+(4*4)+(3*5)+(2*5)+(1*0)=48
48 % 10 = 8
So 10045-50-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NOS/c1-8(13)10-7-12-11(14-10)9-5-3-2-4-6-9/h2-7H,1H3

10045-50-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-Phenyl-1,3-thiazol-5-yl)-1-ethanone

1.2 Other means of identification

Product number -
Other names 1-(2-phenyl-1,3-thiazol-5-yl)ethanone

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:10045-50-8 SDS

10045-50-8Downstream Products

10045-50-8Relevant academic research and scientific papers

CYCLIC SULFAMIDE COMPOUNDS AND METHODS OF USING SAME

-

, (2018/09/21)

The present disclosure provides, in part, cyclic sulfamide compounds, and pharmaceutical compositions thereof, useful as modulators of Hepatitis B (HBV) core protein, and methods of treating Hepatitis B (HBV) infection.

Gyrase inhibitors and uses thereof

-

, (2008/06/13)

The present invention relates to compounds of the formula I: where Ring A is a thiazole, oxazole, imidazole or pyrazole and the substituents are as described in the specification, and pharmaceutically acceptable salts thereof. The compounds inhibit bacter

2-substituted 5-acetyl-4-thiazolyl triflates as useful building blocks for the preparation of functionalized thiazoles

Arcadi, Antonio,Attanasi, Orazio A.,Guidi, Barbara,Rossi, Elisabetta,Santeusanio, Stefania

, p. 3117 - 3126 (2007/10/03)

The readily available 2-substituted 5-acetyl-4-thiazolyl triflates 2 are useful building blocks for the preparation of functionalised thiazoles by means of palladium-catalysed cross-coupling reactions with organometallic reagents and alkoxycarbonylation a

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