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2-(ethoxycarbonylamino)thiophene-3-carboxylic acid is a chemical compound belonging to the thiophene class, characterized by the molecular formula C10H11NO4S. It features a carboxylic acid group and an ethoxycarbonylamino group, which contribute to its potential applications in various fields. 2-(ethoxycarbonylamino)thiophene-3-carboxylic acid's synthesis and properties render it a promising building block for the development of new compounds with biological or chemical activity.

20055-56-5

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20055-56-5 Usage

Uses

Used in Pharmaceutical Industry:
2-(ethoxycarbonylamino)thiophene-3-carboxylic acid is used as a potential building block for the development of new drugs. Its structural features and functional groups make it a valuable candidate for the creation of compounds with biological activity, which can be further explored for therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(ethoxycarbonylamino)thiophene-3-carboxylic acid is utilized as a potential precursor for the synthesis of new agrochemical products. Its unique structure and functional groups can be harnessed to develop compounds with pesticidal, herbicidal, or other agricultural applications, contributing to the advancement of crop protection and management solutions.
Further research and development of 2-(ethoxycarbonylamino)thiophene-3-carboxylic acid may lead to the discovery of new drugs or agrochemical products, expanding its applications and impact on various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 20055-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,5 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20055-56:
(7*2)+(6*0)+(5*0)+(4*5)+(3*5)+(2*5)+(1*6)=65
65 % 10 = 5
So 20055-56-5 is a valid CAS Registry Number.

20055-56-5Downstream Products

20055-56-5Relevant academic research and scientific papers

2-Aryl-5-epoxynitrile anion cyclizations : Total syntheses of (±)-α-cuparenone and (±)-epilaurene

Avila-Zarraga, J. Gustavo,Maldonado, Luis A.

, p. 512 - 513 (2007/10/03)

Total syntheses of the cyclopentane sesquiterpenes of the title using an epoxynitrile anion cyclization reaction as key step, are described. The preferential formation of the cyclopentane ring from a terminal disubstituted 5-epoxynitrile (e.g. 2b) had not previously been observed. The 2-aryl substituent is reasonably assumed to be responsible for this divergence.

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