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5-Isopropyl-thiophene-3-carboxylic acid is a chemical compound characterized by the molecular formula C10H12O2S. It is a carboxylic acid derivative of thiophene, featuring an isopropyl group at the third position. 5-Isopropyl-thiophene-3-carboxylic acid is recognized for its unique chemical structure, which endows it with potential applications across various fields.

123418-51-9

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123418-51-9 Usage

Uses

Used in Pharmaceutical Synthesis:
5-Isopropyl-thiophene-3-carboxylic acid is utilized as an intermediate in the synthesis of a range of pharmaceuticals. Its structure and properties make it a valuable building block for the production of biologically active molecules, contributing to the development of new drugs.
Used in Agrochemical Production:
In the agrochemical industry, 5-Isopropyl-thiophene-3-carboxylic acid serves as an intermediate for the synthesis of various agrochemicals. Its role in this sector is crucial for the creation of compounds that can enhance crop protection and yield.
Used in Organic Compounds Synthesis:
5-Isopropyl-thiophene-3-carboxylic acid is also employed in the synthesis of other organic compounds, highlighting its versatility as a chemical intermediate. Its unique structure allows for the formation of a variety of organic molecules with different applications.
Used in Organic Electronics:
Due to its distinctive chemical makeup, 5-Isopropyl-thiophene-3-carboxylic acid may have potential applications in the field of organic electronics. Its properties could be harnessed in the development of electronic materials and devices.
Used in Materials Science:
In materials science, 5-Isopropyl-thiophene-3-carboxylic acid could be explored for its potential to contribute to the advancement of new materials. Its unique structure may offer novel properties that can be exploited in material development for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 123418-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,1 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123418-51:
(8*1)+(7*2)+(6*3)+(5*4)+(4*1)+(3*8)+(2*5)+(1*1)=99
99 % 10 = 9
So 123418-51-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O2S/c1-5(2)7-3-6(4-11-7)8(9)10/h3-5H,1-2H3,(H,9,10)

123418-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-propan-2-ylthiophene-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-(methylethyl)thiophene-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:123418-51-9 SDS

123418-51-9Downstream Products

123418-51-9Relevant articles and documents

TETRACYCLIC COMPOUNDS AS DOPAMINE AGONISTS

-

, (2008/06/13)

A tetracyclic compound of the formula: STR1 wherein A and the atoms to which it is attached and the optional double bond represent a mono-or di-heterocyclic ring selected from: STR2 wherein R 1, R. sup.2, R 3, R 4 and X are specifically defined, which compounds are useful in the treatment of dopamine-related neurological, psychological and cardiovascular disorders as well as in the treatment of substance abuse and other addictive behavior disorders, cognitive impairment and attention deficit disorder.

Herbicidal Thienylureas, II

Stanetty, Peter,Puschautz, Erhard

, p. 65 - 72 (2007/10/02)

In search of novel biological active thiophene derivatives we recently focused our interest on thienylureas.The present paper deals with substances being in close relation to second generation urea herbicides (C).The main part describes syntheses leading to thiophene carboxylic acids with corresponding substitution patterns.A modified Curtius degradation was used as key step for the formation of the thienylureas. - Keywords: Curtius degradation; Herbicides; Thiophenes; Ureas

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