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4-nitrobenzo[b]thiophene-2-carboxylic acid is a chemical compound with the molecular formula C10H5NO4S. It belongs to the class of benzo[b]thiophene carboxylic acids and features a nitro group and a carboxylic acid group. 4-nitrobenzo[b]thiophene-2-carboxylic acid is known for its aromatic and heterocyclic properties, making it a versatile component in drug discovery and development. It is recognized for its potential in the synthesis of pharmaceuticals and agrochemicals, as well as for its potential anti-cancer, antiviral, and antimicrobial activities, which position it as an important target compound for medicinal chemistry research.

19995-46-1

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19995-46-1 Usage

Uses

Used in Pharmaceutical Industry:
4-nitrobenzo[b]thiophene-2-carboxylic acid is used as a building block for the development of biologically active compounds due to its potential in creating new pharmaceuticals with diverse therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-nitrobenzo[b]thiophene-2-carboxylic acid is utilized as a key intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Medicinal Chemistry Research:
4-nitrobenzo[b]thiophene-2-carboxylic acid is employed as a target compound in medicinal chemistry research for its potential anti-cancer, antiviral, and antimicrobial properties, aiding in the discovery of new therapeutic agents to combat various diseases and infections.

Check Digit Verification of cas no

The CAS Registry Mumber 19995-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,9 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19995-46:
(7*1)+(6*9)+(5*9)+(4*9)+(3*5)+(2*4)+(1*6)=171
171 % 10 = 1
So 19995-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H5NO4S/c11-9(12)8-4-5-6(10(13)14)2-1-3-7(5)15-8/h1-4H,(H,11,12)

19995-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Nitro-1-benzothiophene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-nitrothianaphthene-2-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:19995-46-1 SDS

19995-46-1Relevant academic research and scientific papers

Discovery of fluorescent coumarin-benzo[b]thiophene 1, 1-dioxide conjugates as mitochondria-targeting antitumor STAT3 inhibitors

Cai, Guiping,Yu, Wenying,Song, Dongmei,Zhang, Wenda,Guo, Jianpeng,Zhu, Jiawen,Ren, Yuhao,Kong, Lingyi

, p. 236 - 251 (2019/05/02)

STAT3 has been extensively studied as a potential antitumor target. Though studies on regulating STAT3 mainly focus on the inhibition of STAT3 phosphorylation at Tyr705 residue, the phosphorylation at Ser727 residue of STAT3 protein is also closely associated with the mitochondrial import of STAT3 protein. N, N-diethyl-7-aminocoumarin is a fluorescent mitochondria-targeting probe. In this study, a series of STAT3 inhibitors were developed by connecting N, N-diethyl-7-aminocoumarin fluorophore with benzo [b]thiophene 1, 1-dioxide moiety. All designed compounds displayed potent anti-proliferative activity against cancer cells. The representative compound 7a was mainly accumulated in mitochondria visualized by its fluorescence. STAT3 phosphorylation was inhibited by compound 7a at both Tyr705 and Ser727 residues. Compound 7a inhibited STAT3 phosphorylation whereas had no influence on the phosphorylation levels of STAT1, JAK2, Src and Erk1/2, indicating good selectivity of compound 7a. Moreover, compound 7a down-regulated the expression of STAT3 target genes Bcl-2 and Cyclin D1, increased ROS production and remarkably reduced the mitochondrial membrane potential to induce mitochondrial apoptotic pathway. Furthermore, compound 7a in vivo suppressed breast cancer 4T1 implanted tumor growth. Taken together, these results highlighted that compound 7a might be a promising mitochondria-targeting STAT3 inhibitor for cancer therapy.

METHOD FOR PROMOTING PLANT GROWTH

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Paragraph 0269; 0270, (2015/11/16)

The present invention provides a method for promoting plant growth, which comprises treating a plant with at least one compound selected from a group consisting of a compound represented by the following Formula (1): and an agriculturally acceptable salt thereof, provided that a method for promoting plant growth which comprises treating plants with a compound corresponding to any one of the following (1) to (5) and an agriculturally acceptable salt thereof is excluded: (1) 4-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid, (2) 5-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid, (3) 6-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid, (4) 7-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid, and (5) Benzo[b]thiophene-2-carboxylic acid.

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