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129560-99-2

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129560-99-2 Usage

Description

4-(2,2,2-TRIFLUOROETHOXY)PHENOL is a chemical compound characterized by the molecular formula C8H7F3O2. It is a phenolic compound distinguished by the presence of a trifluoroethoxy group attached to the phenol ring. 4-(2,2,2-TRIFLUOROETHOXY)PHENOL is recognized for its high chemical stability and resistance to various environmental conditions, which makes it a versatile and valuable component in a range of industrial applications.

Uses

Used in Pharmaceutical Industry:
4-(2,2,2-TRIFLUOROETHOXY)PHENOL is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with enhanced properties. Its stability and reactivity make it a suitable candidate for creating complex molecular structures.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(2,2,2-TRIFLUOROETHOXY)PHENOL is utilized as an intermediate in the production of agrochemicals, helping to formulate more effective and stable pesticides and other agricultural chemicals that can withstand environmental conditions.
Used in Polymer and Material Science:
4-(2,2,2-TRIFLUOROETHOXY)PHENOL is used as a building block in the production of polymers and materials, where its stability and chemical properties are leveraged to create materials with specific characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 129560-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,5,6 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129560-99:
(8*1)+(7*2)+(6*9)+(5*5)+(4*6)+(3*0)+(2*9)+(1*9)=152
152 % 10 = 2
So 129560-99-2 is a valid CAS Registry Number.

129560-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,2,2-TRIFLUOROETHOXY)PHENOL

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:129560-99-2 SDS

129560-99-2Relevant articles and documents

THERAPEUTIC AGENT FOR INFLAMMATORY DISEASES, AUTOIMMUNE DISEASES, FIBROTIC DISEASES, AND CANCER DISEASES

-

, (2021/05/06)

A therapeutic agent for treating at least one disease selected from the group consisting of inflammatory diseases, autoimmune diseases, fibrotic diseases, and cancer diseases, comprising: at least one selected from the group consisting of a compound represented by the following general formula (1) and pharmacologically acceptable salts thereof as an active ingredient. [In the formula (1), R1 and R2 may be the same or different and each represents a hydrogen atom, a halogen atom, a hydroxyl group, a carboxy group, a cyano group, an optionally substituted C1-6 alkyl group et al.; R3 represents a hydrogen atom; R4 represents an optionally substituted 4- to 10-membered monocyclic heterocyclic group containing 1 to 4 heteroatoms selected from an oxygen atom, a nitrogen atom, and a sulfur atom; X represents a group represented by the following formula: -CH2-, - CH2-CH2-, -CH2-CH2-CH2-, or -CH2-O-CH2-; and Z represents a hydrogen atom or a hydroxyl group.]

Direct synthesis of anilines and nitrosobenzenes from phenols

St Amant,Frazier,Newmeyer,Fruehauf,Read De Alaniz

supporting information, p. 5520 - 5524 (2016/07/06)

A one-pot synthesis of anilines and nitrosobenzenes from phenols has been developed using an ipso-oxidative aromatic substitution (iSOAr) process. The products are obtained in good yields under mild and metal-free conditions. The leaving group effect on reactions that proceed through mixed quionone monoketals has also been investigated and a predictive model has been established.

(2R)-2-Methylchromane-2-carboxylic acids: Discovery of selective PPARα agonists as hypolipidemic agents

Koyama, Hiroo,Boueres, Julia K.,Miller, Daniel J.,Berger, Joel P.,MacNaul, Karen L.,Wang, Pei-Ran,Ippolito, Marc C.,Wright, Samuel D.,Agrawal, Arun K.,Moller, David E.,Sahoo, Soumya P.

, p. 3347 - 3351 (2007/10/03)

A SAR study was conducted on chromane-2-carboxylic acid toward selective PPARα agonisim. As a result, highly potent, and selective PPARα agonists were discovered. The optimized compound 43 exhibited robust lowering of total cholesterol levels in hamster and dog animal models.

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