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2,4,5-TRIFLUORO-3-HYDROXYBENZOIC ACID METHYL ESTER is a chemical compound characterized by the molecular formula C9H5F3O3. It is a methyl ester derivative of 2,4,5-trifluoro-3-hydroxybenzoic acid, known for its unique properties and versatility in the chemical and pharmaceutical industries. This white crystalline solid, with a melting point of 91-94°C, is soluble in organic solvents and is commonly utilized in the synthesis of various organic compounds.

137234-92-5

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137234-92-5 Usage

Uses

Used in Pharmaceutical Industry:
2,4,5-TRIFLUORO-3-HYDROXYBENZOIC ACID METHYL ESTER is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties. Its unique structure allows for the creation of molecules with targeted actions, enhancing the effectiveness of medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4,5-TRIFLUORO-3-HYDROXYBENZOIC ACID METHYL ESTER is used as a key component in the production of pesticides and other agrochemicals. Its incorporation aids in the development of compounds that can effectively control pests and diseases in agriculture, thus contributing to increased crop yields and protection of plants.
Used in Organic Compounds Synthesis:
2,4,5-TRIFLUORO-3-HYDROXYBENZOIC ACID METHYL ESTER is utilized as a building block in the synthesis of various organic compounds. Its reactivity and structural features make it a valuable precursor for creating a wide array of specialized chemicals used in different industries, including materials science and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 137234-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,2,3 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 137234-92:
(8*1)+(7*3)+(6*7)+(5*2)+(4*3)+(3*4)+(2*9)+(1*2)=125
125 % 10 = 5
So 137234-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F3O3/c1-14-8(13)3-2-4(9)6(11)7(12)5(3)10/h2,12H,1H3

137234-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2,4,5-trifluoro-3-hydroxybenzoate

1.2 Other means of identification

Product number -
Other names 2,4,5-Trifluoro-3-hydroxybenzoic acid 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:137234-92-5 SDS

137234-92-5Relevant academic research and scientific papers

1, 3 - DIHYDROXY SUBSTITUTED PHENYLAMIDE GLUCOKINASE ACTIVATORS

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Page/Page column 80-81, (2009/01/24)

Compounds are provided which are glucokinase activators and thus are useful in treating diabetes and related diseases and have the structure wherein in the ring represents one or two double bonds; R1 is alkyl, aryl, arylalkyl, heteroaryl, or he

Antibacterial agents

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, (2008/06/13)

The present invention provides compounds of formula (I): wherein R1-R6 and J and K have any of the values defined in the specification, and pharmaceutically acceptable salt thereof, that are useful as antibacterial agents. Also disclosed are pharmaceutical compositions comprising one or more compounds of formula I, processes for preparing compounds of formula I, and intermediates useful for preparing compounds of formula I.

Process for preparing alkyl 3-hydroxy-2, 4, 5-trifluorobenzoates and/or alkyl 3-alkoxy-2, 4, 5-trifluorobenzoates

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, (2008/06/13)

The present invention relates to a process for preparing alkyl 3-hydroxy-2,4,5-trifluorobenzoate and/or alkyl 3-alkoxy-2,4,5-trifluorobenzoate by reacting 3-hydroxy-2,4,5-trifluorobenzoic acid with a dialkyl carbonate at 80° to 200° C.

3-Ethenyl, 3-Ethynyl, 3-Aryl, and 3-Cyclopropyl-2,4,5-Trifluorobenzoic Acids: Useful Intermediates In The Synthesis Of Quinolone Antibacterials

Turner, William R.,Suto, Mark J.

, p. 281 - 284 (2007/10/02)

The synthesis of 3-ethenyl, 3-ethynyl, 3-aryl, and 3-cyclopropyl-2,4,5-trifluorobenzoic acids from 1-bromo-2,4,5-trifluorobenzene and 2,4,5-trifluoro-3-hydroxybenzoic acid is described.These compounds are useful intermediates for the synthesis of quinolon

Quinolinecarboxylic acid antibacterial agents

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, (2008/06/13)

Novel 8-alkenyl, alkynyl, allenyl and cycloalkyl-quinolinecarboxylic acids are described as antibacterial agents as well as methods of manufacture including novel intermediates used in said manufacture.

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