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228572-69-8

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228572-69-8 Usage

Description

1-(2-Hydroxy-4-trifluoromethyl-phenyl)-ethanone is a chemical compound characterized by the molecular formula C9H7F3O2. It is a derivative of ketone, featuring a hydroxy group attached to a phenyl ring and a trifluoromethyl group positioned at the 4-position. 1-(2-Hydroxy-4-trifluoroMethyl-phenyl)-ethanone is known for its significance in the fields of organic synthesis and pharmaceutical research.

Uses

Used in Pharmaceutical Research:
1-(2-Hydroxy-4-trifluoroMethyl-phenyl)-ethanone is used as a building block for the preparation of various biologically active molecules. Its unique structure allows for the creation of compounds with potential therapeutic properties, contributing to the development of new drugs and treatments.
Used in Organic Synthesis:
In the realm of organic synthesis, 1-(2-Hydroxy-4-trifluoroMethyl-phenyl)-ethanone serves as a valuable reagent. Its chemical properties make it suitable for use in a range of chemical reactions, particularly in the synthesis of pharmaceuticals and agrochemicals.
Used in Material Science:
1-(2-Hydroxy-4-trifluoroMethyl-phenyl)-ethanone also holds potential in the development of new materials and chemical processes. Its unique properties may be harnessed to create innovative materials with specific characteristics, further expanding its applications across various industries.
Used in Chemical Reactions:
As a reagent, 1-(2-Hydroxy-4-trifluoroMethyl-phenyl)-ethanone is utilized in chemical reactions to facilitate the synthesis of pharmaceuticals and agrochemicals. Its role in these processes is crucial for the production of various compounds with practical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 228572-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,5,7 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 228572-69:
(8*2)+(7*2)+(6*8)+(5*5)+(4*7)+(3*2)+(2*6)+(1*9)=158
158 % 10 = 8
So 228572-69-8 is a valid CAS Registry Number.

228572-69-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-hydroxy-4-(trifluoromethyl)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names -

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:228572-69-8 SDS

228572-69-8Relevant articles and documents

1,4-diphenyl-1H-imidazole and 2,4-diphenyl thiazole derivative and preparation method and use thereof

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Paragraph 0106-0108; 0121-0123, (2019/08/06)

The present invention relates to a 1,4-diphenyl-1H-imidazole and 2,4-diphenyl thiazole derivative having a structure is as follows, wherein R1 is any one of H, OH, OCH3 and the like, R2 is any one ofH, NO2, CH3, CF3, SO2CH3, COOCH3, and CONHCH3, R3 is any

Silanediol-Catalyzed Chromenone Functionalization

Hardman-Baldwin, Andrea M.,Visco, Michael D.,Wieting, Joshua M.,Stern, Charlotte,Kondo, Shin-Ichi,Mattson, Anita E.

supporting information, p. 3766 - 3769 (2016/08/16)

Promising levels of enantiocontrol are observed in the silanediol-catalyzed addition of silyl ketene acetals to benzopyrylium triflates. This rare example of enantioselective, intermolecular chromenone functionalization with carbonyl-containing nucleophiles has potential applications in the synthesis of bioactive chromanones and tetrahydroxanthones.

TRPV1 Antagonists

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Paragraph 0323, (2013/06/28)

Disclosed herein are compounds of formula (I): or pharmaceutically acceptable salts thereof, wherein X1, L, Rx, Ry, Rz, A, m, n, p, q, s, and positions a and b are as defined in the specification. Compositions comprising such compounds and methods for treating conditions and disorders using such compounds and compositions are also disclosed.

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