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2-[2-(3-thienyl)phenyl]acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2004388-06-9

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2004388-06-9 Usage

Derivative of acetic acid

The chemical 2-[2-(3-thienyl)phenyl]acetic acid is a modified version of acetic acid.

Addition of thienyl and phenyl groups

The structure of this chemical includes the addition of a thienyl group and a phenyl group to the acetic acid backbone.

Used in organic synthesis and pharmaceutical research

Due to its potential biological activity, this chemical is commonly used in the creation of new compounds and the study of its potential medicinal properties.

Potential applications in drug development

The chemical's structure and properties make it a promising candidate for the development of new drugs.

Production of advanced materials

The versatility of this chemical's structure allows it to be used in the creation of various compounds with potential industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2004388-06-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,0,0,4,3,8 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2004388-06:
(9*2)+(8*0)+(7*0)+(6*4)+(5*3)+(4*8)+(3*8)+(2*0)+(1*6)=119
119 % 10 = 9
So 2004388-06-9 is a valid CAS Registry Number.

2004388-06-9Downstream Products

2004388-06-9Relevant academic research and scientific papers

Identification of two novel thiophene analogues as inducers of autophagy mediated cell death in breast cancer cells

Gain, Chandrima,Sarkar, Aparna,Bural, Shrea,Rakshit, Moumita,Banerjee, Jeet,Dey, Ankita,Biswas, Nabendu,Kar, Gandhi K.,Saha, Abhik

, (2021)

Natural compounds isolated from different medicinal plants remain one of the major resources of anticancer drugs due to their enormous chemical diversity. Studies suggested therapeutic potential for various tanshinones, key bioactive lipophilic compounds

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