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40889-91-6

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40889-91-6 Usage

Description

2-Chloro-5-(trifluoromethyl)phenol, also known as CFC, is an organic building block derived from phenol. It possesses a yellow liquid appearance and is characterized by the presence of a chlorine atom at the 2nd position and a trifluoromethyl group at the 5th position on the phenol ring. This unique structure endows it with various chemical and physical properties, making it a versatile compound for a wide range of applications.

Uses

Used in Pharmaceutical Industry:
2-Chloro-5-(trifluoromethyl)phenol is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with improved efficacy and reduced side effects. It can be used in the production of antibiotics, anti-inflammatory agents, and other therapeutic molecules.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Chloro-5-(trifluoromethyl)phenol is utilized as a key building block for the development of novel pesticides and herbicides. Its chemical properties enable the creation of compounds with enhanced target specificity, reduced environmental impact, and improved resistance management.
Used in Chemical Synthesis:
2-Chloro-5-(trifluoromethyl)phenol serves as a valuable starting material for the synthesis of various organic compounds, including dyes, polymers, and specialty chemicals. Its reactivity and stability make it an attractive candidate for use in the development of new materials with unique properties and applications.
Used in Material Science:
The unique structure of 2-Chloro-5-(trifluoromethyl)phenol allows it to be used in the development of advanced materials with specific properties. It can be incorporated into the design of new polymers, coatings, and composites with improved mechanical, thermal, and chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 40889-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,8 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40889-91:
(7*4)+(6*0)+(5*8)+(4*8)+(3*9)+(2*9)+(1*1)=146
146 % 10 = 6
So 40889-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C6F14O3/c7-1(8,3(11,12)22-5(15,16)17)21-2(9,10)4(13,14)23-6(18,19)20

40889-91-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L09942)  2-Chloro-5-(trifluoromethyl)phenol, 98%   

  • 40889-91-6

  • 1g

  • 236.0CNY

  • Detail
  • Alfa Aesar

  • (L09942)  2-Chloro-5-(trifluoromethyl)phenol, 98%   

  • 40889-91-6

  • 5g

  • 838.0CNY

  • Detail

40889-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-CHLORO-5-(TRIFLUOROMETHYL)PHENOL

1.2 Other means of identification

Product number -
Other names 2-Chlor-5-trifluormethyl-phenol

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:40889-91-6 SDS

40889-91-6Relevant articles and documents

Novel 2,3-dihydrobenzofuran-2-carboxylic acids: Highly potent and subtype-selective PPARα agonists with potent hypolipidemic activity

Shi, Guo Q.,Dropinski, James F.,Zhang, Yong,Santini, Conrad,Sahoo, Soumya P.,Berger, Joel P.,MacNaul, Karen L.,Zhou, Gaochao,Agrawal, Arun,Alvaro, Raul,Cai, Tian-Quan,Hernandez, Melba,Wright, Samuel D.,Moller, David E.,Heck, James V.,Meinke, Peter T.

, p. 5589 - 5599 (2007/10/03)

The design and synthesis of a novel class of 2,3-dihydrobenzofuran-2- carboxylic acids as highly potent and subtype-selective PPARα agonists are reported. Systematic study of structure-activity relationships has identified several key structural elements within this class for maintaining the potency and subtype selectivity. Select compounds were evaluated in animal models of dyslipidemia using Syrian hamsters and male Beagle dogs, and all these compounds displayed excellent cholesterol- and triglyceride-lowering activity at dose levels that were much lower than the marketed weak PPARα agonist fenofibrate.

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