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ETHYL 4-PHENYL-5-(TRIFLUOROMETHYL)THIOPHENE-2-CARBOXYLATE is a chemical compound with a molecular formula C15H11F3O2S. It is an ester derivative of thiophene carboxylic acid, containing a phenyl group and a trifluoromethyl group. ETHYL 4-PHENYL-5-(TRIFLUOROMETHYL)THIOPHENE-2-CARBOXYLATE is known for its unique properties and potential pharmacological activities, making it a valuable component in organic synthesis and pharmaceutical research.

167279-18-7

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167279-18-7 Usage

Uses

Used in Pharmaceutical Research:
ETHYL 4-PHENYL-5-(TRIFLUOROMETHYL)THIOPHENE-2-CARBOXYLATE is used as a research compound for its potential pharmacological properties. It has been studied for its potential as an anti-inflammatory and anticonvulsant agent, indicating its possible use in the development of medications for treating inflammation and seizure disorders.
Used in Organic Synthesis:
In the field of organic synthesis, ETHYL 4-PHENYL-5-(TRIFLUOROMETHYL)THIOPHENE-2-CARBOXYLATE serves as a key intermediate or building block in the synthesis of more complex organic molecules. Its unique structure, which includes a phenyl and trifluoromethyl group, allows it to participate in various chemical reactions, facilitating the creation of new compounds with specific therapeutic or industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 167279-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,2,7 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 167279-18:
(8*1)+(7*6)+(6*7)+(5*2)+(4*7)+(3*9)+(2*1)+(1*8)=167
167 % 10 = 7
So 167279-18-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H11F3O2S/c1-2-19-13(18)11-8-10(9-6-4-3-5-7-9)12(20-11)14(15,16)17/h3-8H,2H2,1H3

167279-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 4-PHENYL-5-(TRIFLUOROMETHYL)THIOPHENE-2-CARBOXYLATE

1.2 Other means of identification

Product number -
Other names 4-phenyl-5-trifluoromethyl-thiophene-2-carboxylic acid ethyl ester

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:167279-18-7 SDS

167279-18-7Relevant academic research and scientific papers

NOVEL THIOPHENE DERIVATIVES

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Page/Page column 19, (2010/11/25)

The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.

A rational utilization of high-throughput screening affords selective, orally bioavailable 1-benzyl-3-carboxyazetidine sphingosine-1-phosphate-1 receptor agonists

Hale, Jeffrey J.,Lynch, Christopher L.,Neway, William,Mills, Sander G.,Hajdu, Richard,Keohane, Carol Ann,Rosenbach, Mark J.,Milligan, James A.,Shei, Gan-Ju,Parent, Stephen A.,Chrebet, Gary,Bergstrom, James,Card, Deborah,Ferrer, Marc,Hodder, Peter,Strulovici, Berta,Rosen, Hugh,Mandala, Suzanne

, p. 6662 - 6665 (2007/10/03)

Moderately potent, selective S1P1 receptor agonists identified from high-throughput screening have been adapted into lipophilic tails for a class of orally bioavailable amino acid-based S1P1 agonists represented by 7. Many of the new

Microbicidal agents based on thiophene-2-carboxylic acid derivatives

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, (2008/06/13)

PCT No. PCT/EP97/06368 Sec. 371 Date May 26, 1999 Sec. 102(e) Date May 26, 1999 PCT Filed Nov. 14, 1997 PCT Pub. No. WO98/23605 PCT Pub. Date Jun. 4, 1998Novel microbicidal compositions based on thiophene-2-carboxylic acid derivatives, some of which are k

Reactivity of trifluoromethyl enones in Michael additions

Arnaud, Roger,Bensadat, Abdelkader,Ghobsi, Abdelkader,Laurent, Andre,Drean, Isabelle Le,et al.

, p. 844 - 853 (2007/10/02)

A synthesis of trifluoromethyl enones 3 is described. 3a is transformed into the vinyl sulfide 11E,Z.In basic conditions, 11 produces th unusual dihydro-thiophene 10, whose formation from the episulfide 12 is discussed.The natural bonding orbital procedur

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