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2-(TRIFLUOROMETHYL)PHENYL ACETATE is a chemical compound with the molecular formula C10H9F3O2. It is an ester that consists of a phenyl group attached to an acetate group, with a trifluoromethyl substituent at the 2-position of the phenyl ring. 2-(TRIFLUOROMETHYL)PHENYL ACETATE is known for its strong and characteristic odor and is handled and stored with precautions due to its potential hazards.

400629-06-3

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400629-06-3 Usage

Uses

Used in Pharmaceutical Industry:
2-(TRIFLUOROMETHYL)PHENYL ACETATE is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of complex organic molecules with potential medicinal properties.
Used in Agrochemical Industry:
2-(TRIFLUOROMETHYL)PHENYL ACETATE is used as an intermediate in the synthesis of agrochemicals, playing a role in the creation of compounds that can be used in the development of pesticides and other agricultural products.
Used in Organic Compounds Synthesis:
2-(TRIFLUOROMETHYL)PHENYL ACETATE is used as a building block for the preparation of complex organic molecules in chemical research and development, facilitating the creation of new compounds with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 400629-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,6,2 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 400629-06:
(8*4)+(7*0)+(6*0)+(5*6)+(4*2)+(3*9)+(2*0)+(1*6)=103
103 % 10 = 3
So 400629-06-3 is a valid CAS Registry Number.

400629-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(trifluoromethyl)phenyl] acetate

1.2 Other means of identification

Product number -
Other names 2-Acetoxybenzotrifluoride

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:400629-06-3 SDS

400629-06-3Relevant articles and documents

Ligand-Promoted Palladium-Catalyzed C?H Acetoxylation of Simple Arenes

Valderas, Carolina,Naksomboon, Kananat,Fernández-Ibá?ez, M. ángeles

, p. 3213 - 3217 (2016/10/24)

The palladium-catalyzed C?H oxidation of simple arenes is an attractive strategy to obtain phenols, which have many applications in the fine chemicals industry. Although some advances have been made in this research area, low reactivity and selectivity are, in general, observed. This report describes a new catalytic system for the efficient C?H acetoxylation of simple arenes based on Pd(OAc)2 and a pyridinecarboxylic acid ligand.

Steric control of site selectivity in the Pd-catalyzed C-H acetoxylation of simple arenes

Cook, Amanda K.,Emmert, Marion H.,Sanford, Melanie S.

supporting information, p. 5428 - 5431 (2013/11/19)

This report describes the use of an oxidant and a ligand to control site selectivity in the Pd(OAc)2-catalyzed C-H acetoxylation of simple arenes. The use of MesI(OAc)2 as the terminal oxidant in combination with acridine as the ligand results in primarily sterically controlled selectivity. In contrast, with Pd(OAc)2 as the catalyst and PhI(OAc)2 as the oxidant, electronic effects dominate the selectivity of arene C-H acetoxylation.

NOVEL PHENOL DERIVATIVE

-

Page/Page column 29, (2012/07/28)

Disclosed are a novel compound and a pharmaceutical product, each having a remarkable uricosuric effect. Specifically disclosed are: a novel phenol derivative represented by general formula (1) that is shown in FIG. 1; a pharmaceutically acceptable salt t

Remarkably high reactivity of Pd(OAc)2/pyridine catalysts: Nondirected C-H oxygenation of arenes

Emmert, Marion H.,Cook, Amanda K.,Xie, Yushu J.,Sanford, Melanie S.

supporting information; experimental part, p. 9409 - 9412 (2011/11/07)

Less is more: The rational optimization and general applicability of the catalytic system Pd(OAc)2/pyridine is described (see scheme). The catalyst shows excellent reactivity in the C-H oxygenation of simple aromatic substrates. The Pd/pyridine ratio is critical as the use of one equivalent of pyridine per Pd center leads to dramatic enhancements in both reactivity and site selectivity in comparison to Pd(OAc)2 alone.

Platinum and palladium complexes containing cationic ligands as catalysts for arene H/D exchange and oxidation

Emmert, Marion H.,Gary, J. Brannon,Villalobos, Janette M.,Sanford, Melanie S.

supporting information; experimental part, p. 5884 - 5886 (2010/11/19)

Cationic catalysts in HD: Palladium(II) and platinum(II) complexes of pyridinium-substituted bipyridine ligands are highly active and stable catalysts for H/D exchange and oxidation of aromatic C-H bonds (TONs up to 3200, TOFs up to 0.1 s-1; se

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