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168833-80-5

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168833-80-5 Usage

Description

3-(TRIFLUOROMETHOXY)CINNAMIC ACID, also known as trans-3-(Trifluoromethoxy)cinnamic Acid, is an off-white crystalline powder with unique chemical properties. It is a synthetic organic compound characterized by the presence of a trifluoromethoxy group attached to a cinnamic acid backbone. 3-(TRIFLUOROMETHOXY)CINNAMIC ACID exhibits significant potential in various applications due to its distinct chemical structure and properties.

Uses

Used in Pharmaceutical Industry:
3-(TRIFLUOROMETHOXY)CINNAMIC ACID is used as an intermediate compound for the synthesis of pharmaceuticals targeting dysproliferative diseases. Its unique structure allows it to interact with biological systems in ways that can help regulate cell proliferation, making it a valuable component in the development of treatments for conditions characterized by abnormal cell growth.
Used in Antioxidant Formulations:
In the field of chemistry and material science, 3-(TRIFLUOROMETHOXY)CINNAMIC ACID is used as a plating agent for compounds that possess antioxidant properties. Its ability to enhance the stability and effectiveness of antioxidants can be beneficial in various applications, such as in the food industry to extend the shelf life of products, or in the cosmetic industry to protect against oxidative stress and promote skin health.
Used in Research and Development:
3-(TRIFLUOROMETHOXY)CINNAMIC ACID also serves as a valuable research tool in academic and industrial laboratories. Its unique chemical properties make it an interesting subject for studies aimed at understanding its reactivity, potential applications, and mechanisms of action. This can lead to the discovery of new uses and the development of novel products and technologies based on this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 168833-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,8,3 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 168833-80:
(8*1)+(7*6)+(6*8)+(5*8)+(4*3)+(3*3)+(2*8)+(1*0)=175
175 % 10 = 5
So 168833-80-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H7F3O3/c11-10(12,13)16-8-3-1-2-7(6-8)4-5-9(14)15/h1-6H,(H,14,15)/p-1/b5-4+

168833-80-5 Well-known Company Product Price

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  • TCI America

  • (T1780)  3-(Trifluoromethoxy)cinnamic Acid  >98.0%(T)

  • 168833-80-5

  • 5g

  • 1,300.00CNY

  • Detail
  • TCI America

  • (T1780)  3-(Trifluoromethoxy)cinnamic Acid  >98.0%(T)

  • 168833-80-5

  • 25g

  • 5,500.00CNY

  • Detail
  • Alfa Aesar

  • (B21560)  3-(Trifluoromethoxy)cinnamic acid, 96%   

  • 168833-80-5

  • 0.25g

  • 218.0CNY

  • Detail
  • Alfa Aesar

  • (B21560)  3-(Trifluoromethoxy)cinnamic acid, 96%   

  • 168833-80-5

  • 1g

  • 304.0CNY

  • Detail
  • Alfa Aesar

  • (B21560)  3-(Trifluoromethoxy)cinnamic acid, 96%   

  • 168833-80-5

  • 5g

  • 1029.0CNY

  • Detail

168833-80-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(TRIFLUOROMETHOXY)CINNAMIC ACID

1.2 Other means of identification

Product number -
Other names 3-(3-(Trifluoromethoxy)phenyl)acrylic acid

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:168833-80-5 SDS

168833-80-5Relevant articles and documents

Dual Nickel/Ruthenium Strategy for Photoinduced Decarboxylative Cross-Coupling of α,β-Unsaturated Carboxylic Acids with Cycloketone Oxime Esters

Lu, Xiao-Yu,Xia, Ze-Jie,Gao, Ang,Liu, Qi-Le,Jiang, Run-Chuang,Liu, Chuang-Chuang

supporting information, p. 8829 - 8842 (2021/06/30)

Herein, a dual nickel/ruthenium strategy is developed for photoinduced decarboxylative cross-coupling between α,β-unsaturated carboxylic acids and cycloketone oxime esters. The reaction mechanism is distinct from previous photoinduced decarboxylation of α,β-unsaturated carboxylic acids. This reaction might proceed through a nickelacyclopropane intermediate. The C(sp2)-C(sp3) bond constructed by the aforementioned reaction provides an efficient approach to obtaining various cyanoalkyl alkenes, which are synthetically valuable organic skeletons in organic and medicinal chemistry, under mild reaction conditions. The protocol tolerates many critical functional groups and provides a route for the modification of complex organic molecules.

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