25785-09-5 Usage
Description
5-NITRO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID ETHYL ESTER is a chemical compound with the molecular formula C12H9NO4S. It is an ethyl ester derivative of 5-nitrobenzothiophene-2-carboxylic acid, known for its various pharmacological properties such as antimicrobial and antifungal activities. 5-NITRO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID ETHYL ESTER is commonly used in organic synthesis and pharmaceutical research, serving as a building block in the synthesis of various pharmaceuticals and agrochemicals. However, due to its potential toxicity and health hazards, it is crucial to handle this compound with proper care and in accordance with safety guidelines.
Uses
Used in Organic Synthesis:
5-NITRO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID ETHYL ESTER is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and functional groups make it a valuable building block for the development of new molecules with potential applications in various fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-NITRO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID ETHYL ESTER is used as a starting material for the development of new drugs. Its pharmacological properties, such as antimicrobial and antifungal activities, make it a promising candidate for the treatment of various infections and diseases.
Used in Agrochemicals:
5-NITRO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID ETHYL ESTER is also used in the agrochemical industry as a precursor for the synthesis of various agrochemicals. Its antimicrobial and antifungal properties can be utilized in the development of pesticides and fungicides to protect crops from diseases and pests.
Used in Antimicrobial Applications:
5-NITRO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID ETHYL ESTER is used as an antimicrobial agent for the treatment of bacterial and fungal infections. Its broad-spectrum activity makes it a potential candidate for the development of new antimicrobial drugs to combat drug-resistant pathogens.
Used in Antifungal Applications:
In the field of antifungal research, 5-NITRO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID ETHYL ESTER is used as an antifungal agent to treat various fungal infections. Its ability to inhibit fungal growth and proliferation makes it a valuable compound for the development of new antifungal drugs and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 25785-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,8 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25785-09:
(7*2)+(6*5)+(5*7)+(4*8)+(3*5)+(2*0)+(1*9)=135
135 % 10 = 5
So 25785-09-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO4S/c1-2-16-11(13)10-6-7-5-8(12(14)15)3-4-9(7)17-10/h3-6H,2H2,1H3
25785-09-5Relevant articles and documents
A straightforward expeditious synthesis of 5-nitrobenzo[b]thiophene-2- carbaldehyde
Wei, Hongtao,Sun, Min,Ji, Min
, p. 359 - 360 (2009)
A high yielding one-pot synthesis of 5-nitrobenzo[b]thiophene-2- carbaldehyde is reported using the readily available,cheap starting material 2,5-dihydroxy-1,4-dithiane and 2-chloro-5-nitrobenzaldehyde.
Design, synthesis, and biological evaluation of novel benzo[b]thiophene-diaryl urea derivatives as potential anticancer agents
Zarei, Omid,Azimian, Fereshteh,Hamzeh-Mivehroud, Maryam,Shahbazi Mojarrad, Javid,Hemmati, Salar,Dastmalchi, Siavoush
, p. 1438 - 1448 (2020/05/28)
A hybrid pharmacophore approach was applied to design and synthesize a series of benzo[b]thiophene-diaryl urea derivatives 17a–g with potential anticancer effect. In vitro antiproliferative activities of all target compounds were evaluated against HT-29 a
Design, synthesis, and in vitro antiproliferative activity of novel Dasatinib derivatives
Cai, Jin,Zhang, Shaoning,Zheng, Ming,Wu, Xiaoqing,Chen, Junqing,Ji, Min
scheme or table, p. 806 - 810 (2012/03/26)
Two series of novel Dasatinib derivatives have been designed and synthesized, with their in vitro cytostatic effect screened on human chronic myeloid leukemia cell line K562 and human myeloid leukemia cell line U937. Some target compounds demonstrated sig