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METHYL 3-HYDROXY-5-TRIFLUOROMETHYLTHIOPHENE-2-CARBOXYLATE is a chemical compound with the molecular formula C8H5F3O3S. It is a derivative of thiophene, a five-membered heterocyclic compound containing sulfur. The presence of a hydroxy and a carboxylic ester group in the compound suggests its potential use in pharmaceutical and medicinal chemistry. The trifluoromethyl group can affect the physicochemical properties and reactivity of the compound, making it valuable for various applications in organic synthesis and drug discovery.
Used in Pharmaceutical Industry:
METHYL 3-HYDROXY-5-TRIFLUOROMETHYLTHIOPHENE-2-CARBOXYLATE is used as a building block for the development of new drugs and agrochemicals due to its unique structure and functional groups.
Used in Medicinal Chemistry:
METHYL 3-HYDROXY-5-TRIFLUOROMETHYLTHIOPHENE-2-CARBOXYLATE is used as a key intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of novel therapeutic agents.
Used in Organic Synthesis:
METHYL 3-HYDROXY-5-TRIFLUOROMETHYLTHIOPHENE-2-CARBOXYLATE is used as a versatile reagent in organic synthesis, enabling the creation of a wide range of chemical products.
Used in Drug Discovery:
METHYL 3-HYDROXY-5-TRIFLUOROMETHYLTHIOPHENE-2-CARBOXYLATE is used as a potential candidate in drug discovery, with its unique structure and functional groups offering opportunities for the development of innovative therapeutic agents.

157162-16-8

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157162-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157162-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,1,6 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 157162-16:
(8*1)+(7*5)+(6*7)+(5*1)+(4*6)+(3*2)+(2*1)+(1*6)=128
128 % 10 = 8
So 157162-16-8 is a valid CAS Registry Number.

157162-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-hydroxy-5-(trifluoromethyl)thiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-thiophenecarboxylic acid,3-hydroxy-5-(trifluoromethyl)-,methyl 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:157162-16-8 SDS

157162-16-8Relevant academic research and scientific papers

Preparation of 4-hydroxy-2-trifluoromethylthiophene: A novel bioisostere of α,α,α-trifluoro-m-cresol

Karp, Gary M.,Samant, Dilip,Mukhopadhyay, Sudarsan,Condon, Michael E.,Kleemann, Axel

, p. 1078 - 1080 (2000)

A simple and convenient four-step synthesis of 4-hydroxy-2- trifluoromethylthiophene (1) a novel bioisostere of α,α,α- trifluoro-m-cresol is reported. The key step is the condensation between ethyl 3-methoxy-4,4,4-trifluorocrotonate and methyl thioglycolate to form methyl 3-hydroxy-5- trifluoromethylthiophene-2-carboxylate (6). Hydrolysis of the ester followed by decarboxylation furnishes 1. Multi-hundred gram quantities of 1 have been obtained utilizing the present procedure.

An effective synthesis of 2-trifluoromethyl- or 2-(1,1-difluoroalkyl)thiophenes

Guan, Hui-Ping,Luo, Bing-Hao,Hu, Chang-Ming

, p. 461 - 464 (1997)

Various thiophenecarboxylates carrying a 2-trifluoromethyl, 2-(1,1-difluoroalkyl) or 2-polyfluoroalkyl group are synthesized conveniently from reaction of α-fluoroalkyl ketones 1, aldehydes 2 or ethyl α-fluoroalkylacetates 3 with methyl (or ethyl) 2-sulfa

Thienyloxypyridines and-pyrimidines useful as herbicidal agents

-

, (2008/06/13)

The present invention provides a herbicidal compound of formula I, methods for the preparation thereof and intermediates useful therefor. wherein X and Y are each independently O or S; Z is N or CR4.

Herbicidal pyridine compounds

-

, (2008/06/13)

The novel compounds of formula I: wherein R, A, X1, X2, X3, Z and m have the meaning given in claim 1, and the agronomically acceptable salts or N-oxides thereof, and herbicidal compositions containing such compounds as active ingredients.

Herbicidal 2-(cycloalk(en)yloxy)-6-(hetero)aryloxy(thio)pyridines

-

, (2008/06/13)

The novel compounds of formula I: wherein R, A, X1, X2, X3and Z have the meaning given in claim 1, and the agronomically acceptable salts or N-oxide thereof, and herbicidal compositions containing such compounds as active ingredients.

Herbicidal pyridine compounds

-

, (2008/06/13)

The novel compounds of formula I: wherein one of the groups X1, X2and X3represents N or CR1and the others represent CR1; R1each independently represents a hydrogen or halogen atom or an optionally substituted alkyl, alkenyl, alkinyl, alkoxy, alkoxyalkyl, alkoxyalkoxy group or a haloalkyl, haloalkoxy, cyano, nitro or SF5group, or -S(O)p-R10in which p is 0, 1 or 2 and R10represents an alkyl or haloalkyl group, or -NR2R3in which R2and R3each independently represent a hydrogen atom, an alkyl, alkenyl, aralkyl or aryl group, or R4-O-C(Y)- in which R4represents an alkyl group and Y represents O or S; A represents an optionally substituted aryl group, an optionally substituted 5- or 6- membered nitrogen-containing heteroaromatic group or an optionally substituted thienyl group; R represents an optionally substituted haloalkyl or haloalkenyl group; m is 0, 1, 2 or 3; Z represents an oxygen or sulfur atom; and the agronomically acceptable salts or N-oxides thereof; with the proviso that R represents an optionally substituted haloalkenyl group when m is 0. and herbicidal compositions containing such compounds as active ingredients.

Herbicidal thienyloxyazines

-

, (2008/06/13)

A compound is disclosed having the formula: STR1 The compound is useful as an active ingredient in a herbicidal composition.

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