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3-Pentafluorophenyl-propionic acid ethyl ester is an organic compound with the chemical formula C9H7F5O2. It is a colorless liquid at room temperature and is derived from the esterification of 3-pentafluorophenyl-propionic acid with ethanol. 3-PENTAFLUOROPHENYL-PROPIONIC ACID ETHYL ESTER is characterized by its strong electron-withdrawing pentafluorophenyl group, which makes it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and stability, it is often used in the preparation of active ingredients and functional materials. The compound is also known for its potential applications in materials science, particularly in the development of new polymers and coatings.

2828-18-4

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2828-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2828-18-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2828-18:
(6*2)+(5*8)+(4*2)+(3*8)+(2*1)+(1*8)=94
94 % 10 = 4
So 2828-18-4 is a valid CAS Registry Number.

2828-18-4SDS

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 ethyl 3-(2,3,4,5,6-pentafluorophenyl)propanoate

1.2 Other means of identification

Product number -
Other names ethyl-3-pentafluorophenyl-2-propanoate

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:2828-18-4 SDS

2828-18-4Relevant academic research and scientific papers

Rh(I)-Catalyzed olefin hydroarylation with electron-deficient perfluoroarenes

Sun, Zhong-Ming,Zhang, Jing,Manan, Rajith S.,Zhao, Pinjing

supporting information; experimental part, p. 6935 - 6937 (2010/08/06)

Assisted by a partially aqueous media, a catalyst system of [Rh(cod)(OH)]2 and DPPBenzene ligand effectively promotes direct conjugate additions by perfluoroarenes. This formal C-H alkylation process represents a rare example of olefin hydroarylation with electron-deficient arenes. The catalyst system can be modified to selectively form the corresponding olefination products under anhydrous conditions.

2,5-Disubstituted tetrahydrofurans as selective serotonin re-uptake inhibitors

Voelker, Troy,Xia, Haiji,Fandrick, Keith,Johnson, Robert,Janowsky, Aaron,Cashman, John R.

experimental part, p. 2047 - 2068 (2009/06/06)

Enhancement of 5-hydroxytryptamine (5-HT, serotonin) neurotransmission is a viable means of treating depression. On the basis of this observation, agents that inhibit re-uptake of 5-HT were prepared based on (-)-cocaine and aryltropanes as lead compounds

MODULATORS OF CENTRAL NERVOUS SYSTEM NEUROTRANSMITTERS

-

Page/Page column 90, (2010/10/20)

Disclosed are agents having pharmacological activity against cellular receptors and intracellular singaling, particularly receptors and sigaling pathways of central nervous system (CNS) neurotransmitters. Also disclosed are related methods and compositions for the treatment or prevention of diseases or disorders using the agents.

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