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4-Methylthiophene-3-carboxylic acid is a chemical compound with the molecular formula C7H6OS, belonging to the thiophene family of five-membered heterocyclic compounds that contain sulfur. Its structure features a carboxylic acid group, classifying it as an organic acid. 4-Methylthiophene-3-carboxylic acid is known for its significant role in the field of organic chemistry due to its versatile applications across various industries.

78071-30-4

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78071-30-4 Usage

Uses

Used in Pharmaceutical Industry:
4-Methylthiophene-3-carboxylic acid is used as a building block for the synthesis of various drugs. Its unique structure allows it to be a key component in the development of new pharmaceuticals, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Methylthiophene-3-carboxylic acid serves as a precursor in the production of pesticides. Its properties make it suitable for the creation of effective compounds aimed at controlling pests and enhancing crop protection.
Used in Flavor and Fragrance Industry:
4-Methylthiophene-3-carboxylic acid is utilized in the formulation of flavors and fragrances. Its distinctive chemical structure imparts specific scents and tastes, making it valuable in the development of a wide range of products within this industry.
Used as an Intermediate in Organic Synthesis:
4-Methylthiophene-3-carboxylic acid also plays a crucial role as an intermediate in the synthesis of other organic compounds. Its reactivity and functional groups make it a versatile building block for creating a variety of organic molecules for different applications.
Overall, 4-Methylthiophene-3-carboxylic acid's applications in the pharmaceutical, agrochemical, flavor and fragrance, and organic synthesis industries highlight its importance and versatility in the realm of organic chemistry and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 78071-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,7 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78071-30:
(7*7)+(6*8)+(5*0)+(4*7)+(3*1)+(2*3)+(1*0)=134
134 % 10 = 4
So 78071-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O2S/c1-4-2-9-3-5(4)6(7)8/h2-3H,1H3,(H,7,8)

78071-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methylthiophene-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-METHYLTHIOPHENE-3-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:78071-30-4 SDS

78071-30-4Relevant academic research and scientific papers

PYRAZOLE AMIDE DERIVATIVE

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Page/Page column 78, (2015/09/28)

The present invention relates to a novel compound having a function of inhibiting RORγ activity. The present invention also relates to pharmaceutical composition comprising the compound, a use of the compound in treating or preventing autoimmune diseases, inflammatory diseases, metabolic diseases, or cancer diseases.

ACC INHIBITORS AND USES THEREOF

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, (2014/12/09)

The present invention provides compounds useful as inhibitors of Acetyl CoA Carboxylase (ACC), compositions thereof, and methods of using the same.

Lignan analogues, methods of preparation thereof and anti-hyperlipemic agents

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, (2008/06/13)

An anti-hyperlipemic agent which has a potent activity of reducing LDL and VLDL cholesterols, which are thought to be a risk factor for arteriosclerosis among total blood cholesterols, and which is excellent in the antioxidant activity on LDL, is provided. Additionally, a compound and a pharmaceutically acceptable salt thereof are disclosed, which is represented by Formula (I): STR1 [wherein R1 is a power alkyl, cycloalkyl, cycloalkyl-lower alkyl, aryl or aralkyl group which is optionally substituted; R2 is a group represented by the formula: --COOR' (wherein R' is a lower alkyl or aralkyl which is optionally substituted), lower alkyl or halogenated lower alkyl; or R1 and R2, together with adjacent carbonyl group, form a cyclohexanone ring represented by the formula: STR2 R3 is a phenyl group optionally being substituted, and, ring A is a benzene nucleus which is optionally substituted, or a heterocyclic ring containing S or O optionally being substituted].

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