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124811-71-8

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124811-71-8 Usage

Description

4-HYDROXY-3-(TRIFLUOROMETHYL)BENZONITRILE is a white crystalline compound that serves as an intermediate in organic syntheses. It is characterized by the presence of a hydroxyl group, a trifluoromethyl group, and a nitrile group attached to a benzene ring. This unique structure endows it with versatile chemical properties, making it a valuable component in various applications.

Uses

Used in Organic Syntheses:
4-HYDROXY-3-(TRIFLUOROMETHYL)BENZONITRILE is used as an intermediate in organic syntheses for the production of various chemical compounds. Its reactive functional groups allow for a wide range of chemical reactions, making it a useful building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in High Voltage Lithium-Ion Batteries:
In the energy industry, 4-HYDROXY-3-(TRIFLUOROMETHYL)BENZONITRILE is used as a novel electrolyte additive for lithium nickel manganese oxide cathode of high voltage lithium-ion batteries. Its addition to the electrolyte helps to improve the battery's performance and stability by forming a low-impedance protective film on the electrode surface. This protective film reduces the impedance and enhances the overall efficiency of the battery, making it suitable for high voltage applications.
Used in Chemical Research:
4-HYDROXY-3-(TRIFLUOROMETHYL)BENZONITRILE is also used in chemical research as a model compound to study the reactivity and properties of various functional groups. Its unique structure allows researchers to investigate the effects of electron-withdrawing and electron-donating groups on the chemical behavior of the molecule, providing valuable insights into the design of new chemical compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 124811-71-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,8,1 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124811-71:
(8*1)+(7*2)+(6*4)+(5*8)+(4*1)+(3*1)+(2*7)+(1*1)=108
108 % 10 = 8
So 124811-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H4F3NO/c9-8(10,11)6-3-5(4-12)1-2-7(6)13/h1-3,13H

124811-71-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H31639)  4-Hydroxy-3-(trifluoromethyl)benzonitrile, 98+%   

  • 124811-71-8

  • 1g

  • 873.0CNY

  • Detail
  • Alfa Aesar

  • (H31639)  4-Hydroxy-3-(trifluoromethyl)benzonitrile, 98+%   

  • 124811-71-8

  • 5g

  • 3711.0CNY

  • Detail

124811-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydroxy-3-(trifluoromethyl)benzonitrile

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-3-(Trifluoromethyl)Benzonitrile

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:124811-71-8 SDS

124811-71-8Relevant articles and documents

Cu and hydroquinone for the trifluoromethylation of unprotected phenols

Pletz, Jakob,Koeberl, Christoph,Fuchs, Michael,Steiner, Oliver,Goessler, Walter,Kroutil, Wolfgang

, p. 682 - 690 (2019)

Fluorination and trifluoromethylation are indispensable tools in the preparation of modern pharmaceuticals and APIs. Herein we present a concept for the introduction of a trifluoromethyl group into unprotected phenols employing catalytic copper(I) iodide

Photoinduced Hydroxylation of Organic Halides under Mild Conditions

Cai, Yue-Ming,Xu, Yu-Ting,Zhang, Xin,Gao, Wen-Xia,Huang, Xiao-Bo,Zhou, Yun-Bing,Liu, Miao-Chang,Wu, Hua-Yue

supporting information, p. 8479 - 8484 (2019/10/16)

Presented in this paper is photoinduced hydroxylation of organic halides, providing a mild access to a range of functionalized phenols and aliphatic alcohols. These reactions generally proceed under mild reaction conditions with no need for a photocatalyst or a strong base and show a wide substrate scope as well as excellent functional group tolerance. This work highlights the unique role of NaI that allows a challenging transformation to proceed under mild reaction conditions.

NOVEL OXADIAZOLE COMPOUNDS

-

Page/Page column 169, (2011/06/26)

Novel oxadiazole compounds, pharmaceutical compositions containing such compounds and the use of those compounds or compositions as agonists or antagonists of the S1P family of G protein-coupled receptors for treating diseases associated with modulation o

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