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7-Fluorobenzo[b]thiophene-2-carboxylic acid is a fluorinated heterocyclic aromatic compound with the molecular formula C9H5FO2S. It is a derivative of benzo[b]thiophene-2-carboxylic acid, known for its unique structural features and potential biological activities, such as antimicrobial and anticancer properties. This chemical compound serves as a valuable building block in the synthesis of pharmaceuticals and agrochemicals, and has also been explored for its applications in materials science and organic electronics due to its intriguing electronic and optical properties.

550998-67-9

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550998-67-9 Usage

Uses

Used in Pharmaceutical Industry:
7-Fluorobenzo[b]thiophene-2-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its potential biological activities. Its unique structure allows for the development of new drugs with improved therapeutic effects and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical industry, 7-Fluorobenzo[b]thiophene-2-carboxylic acid is utilized as a building block for the synthesis of novel agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds while minimizing environmental impact.
Used in Materials Science:
7-Fluorobenzo[b]thiophene-2-carboxylic acid is employed in materials science for its interesting electronic and optical properties. It can be used to develop new materials with enhanced performance in various applications, such as sensors, solar cells, and electronic devices.
Used in Organic Electronics:
In the field of organic electronics, 7-Fluorobenzo[b]thiophene-2-carboxylic acid is used as a component in the design and synthesis of organic semiconductors. Its electronic properties make it suitable for applications in organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and organic photovoltaics (OPVs), contributing to the development of flexible and efficient electronic devices.

Check Digit Verification of cas no

The CAS Registry Mumber 550998-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,0,9,9 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 550998-67:
(8*5)+(7*5)+(6*0)+(5*9)+(4*9)+(3*8)+(2*6)+(1*7)=199
199 % 10 = 9
So 550998-67-9 is a valid CAS Registry Number.

550998-67-9SDS

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 7-Fluoro-1-benzothiophene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names GA-0926

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:550998-67-9 SDS

550998-67-9Upstream product

550998-67-9Relevant academic research and scientific papers

COMPOUNDS FOR THE TREATMENT OF PARAMOXYVIRUS VIRAL INFECTIONS

-

, (2014/03/25)

Disclosed herein are new antiviral compounds, together with pharmaceutical compositions that include one or more antiviral compounds, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a paramyxovirus viral infection with one or more small molecule compounds. Examples of paramyxovirus infection include an infection caused by human respiratory syncytial virus (RSV).

C17,20-lyase inhibitors I. Structure-based de novo design and SAR study of C17,20-lyase inhibitors.

Matsunaga, Nobuyuki,Kaku, Tomohiro,Itoh, Fumio,Tanaka, Toshimasa,Hara, Takahito,Miki, Hiroshi,Iwasaki, Masahiko,Aono, Tetsuya,Yamaoka, Masuo,Kusaka, Masami,Tasaka, Akihiro

, p. 2251 - 2273 (2007/10/03)

Novel nonsteroidal C(17,20)-lyase inhibitors were synthesized using de novo design based on its substrate, 17 alpha-hydroxypregnenolone, and several compounds exhibited potent C(17,20)-lyase inhibition. However, in vivo activities were found to be short-lasting, and in order to improve the duration of action, a series of benzothiophene derivatives were evaluated. As a result, compounds 9h, (S)-9i, and 9k with nanomolar enzyme inhibition (IC(50)=4-9 nM) and 9e (IC(50)=27 nM) were identified to have powerful in vivo efficacy with extended duration of action. The key structural determinants for the in vivo efficacy were demonstrated to be the 5-fluoro group on the benzothiophene ring and the 4-imidazolyl moiety. Superimposition of 9k and 17 alpha-hydroxypregnenolone demonstrated their structural similarity and enabled rationalization of the pharmacological results. In addition, selected compounds were also identified to be potent inhibitors of human enzyme with IC(50) values of 20-30 nM.

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