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4-Bromo-3-methylthiophenecarboxylic acid is a chemical compound characterized by its unique molecular structure, featuring a phenyl ring with a single bromine atom substitution, a methylthio group, and a carboxylic acid functional group. With a scientific formula of C6H5BrO2S, 4-Bromo-3-methylthiophenecarboxylic acid is widely utilized in the synthesis of other chemical compounds, making it a valuable asset in the field of organic chemistry. Its reactivity and stability are largely influenced by the presence of bromine and carboxylic acid functional groups, which enable it to participate in a variety of chemical reactions.

265652-39-9

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265652-39-9 Usage

Uses

Used in Organic Chemistry:
4-Bromo-3-methylthiophenecarboxylic acid is used as a synthetic intermediate for the production of various chemical compounds. Its bromine and carboxylic acid functional groups allow it to participate in a wide range of reactions, making it a versatile building block in organic synthesis.
Used in Pharmaceutical Industry:
4-Bromo-3-methylthiophenecarboxylic acid is used as a key component in the development of pharmaceutical compounds. Its unique structure and functional groups can be exploited to create new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Bromo-3-methylthiophenecarboxylic acid is used as a precursor for the synthesis of various agrochemicals, such as pesticides and herbicides. Its reactivity and stability make it suitable for the development of effective and environmentally friendly agrochemical products.
Used in Dye and Pigment Industry:
4-Bromo-3-methylthiophenecarboxylic acid is used as a starting material for the synthesis of dyes and pigments. Its bromine atom and phenyl ring structure contribute to the color properties of the resulting dyes and pigments, making it a valuable component in this industry.
Used in Material Science:
In the field of material science, 4-Bromo-3-methylthiophenecarboxylic acid is used for the development of new materials with specific properties. Its functional groups can be utilized to create materials with improved stability, reactivity, or other desired characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 265652-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,5,6,5 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 265652-39:
(8*2)+(7*6)+(6*5)+(5*6)+(4*5)+(3*2)+(2*3)+(1*9)=159
159 % 10 = 9
So 265652-39-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrO2S/c1-3-4(7)2-10-5(3)6(8)9/h2H,1H3,(H,8,9)

265652-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-3-methylthiophene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-bromo-3-methyl-thiophene-2-carboxylic Acid

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:265652-39-9 SDS

265652-39-9Relevant academic research and scientific papers

FUSED THIOPHENE COMPOUNDS

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Paragraph 0142, (2020/01/08)

The present disclosure provides compounds that modulate protein function of 1 L-1β, IL-2, IL-6, TNF-α, CK1α, GSPT1, aiolos, ikaros or helios, to restore protein homeostasis, and 1 cell-cell adhesion. The disclosure provides methods of modulating protein-mediated diseases, such as cytokine-mediated diseases, disorders, conditions, or responses. Compositions, including in combination with other cytokine and inflammatory mediators are provided. Uses of compounds for treatment or amelioration of diseases, disorders, or conditions associated with a protein, are also provided.

3-(PYRIDIN-3-YL)-ACRYLAMIDE AND N-(PYRIDIN-3-YL)-ACRYLAMIDE DERIVATIVES AND THEIR USE AS PAK OR NAMPT MODULATORS

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, (2017/03/14)

The invention generally relates to cyclic compounds and, more particularly, to a compound represented by Structural Formula I: or a pharmaceutically acceptable salt thereof and pharmaceutical compositions comprising the multicyclic compounds. The invention also relates to a method for treating a disease or disorder selected from cancer (e.g., lymphoma, such as mantle cell lymphoma), a neurodegenerative disease, an inflammatory diseases or an immune system disease (e.g., a T- Cell mediated autoimmune diseases) in a subject in need thereof. The method comprises administering to a subject in need thereof a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, or a composition comprising a compound of the invention, or a pharmaceutically acceptable salt thereof.

Process for preparing 3-(substituted phenyl)-5-thienyl or furyl)-1,2,4-triazoles and novel intermediates utilized therein

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, (2008/06/13)

New synthetic procedures for preparing insecticidal 3-(substituted phenyl)-5-(thienyl or furyl)-1,2,4-triazoles utilizing thioimidate intermediate.

3-(substituted phenyl)-5-thienyl-1,2,4-triazole compounds with activity against whitefly

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, (2008/06/13)

3-(Substituted phenyl)-5-(thienyl)-1,2,4-triazole compounds are useful as insecticides and acaricides.

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