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2-Bromothieno[2,3-b]pyridine, with the molecular formula C8H5BrNS, is a heterocyclic aromatic compound characterized by the presence of a bromine atom and a thiophene ring fused to a pyridine ring. This unique structure endows it with potential pharmacological properties, making it a valuable compound in the fields of organic synthesis and pharmaceutical research.

72808-92-5

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72808-92-5 Usage

Uses

Used in Organic Synthesis:
2-Bromothieno[2,3-b]pyridine serves as a versatile building block in organic synthesis, facilitating the creation of various biologically active compounds. Its unique structure allows for the development of novel molecules with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Bromothieno[2,3-b]pyridine is utilized as a precursor for the preparation of potential anticancer agents and other pharmaceuticals. Its ability to be incorporated into the molecular structures of these agents contributes to the discovery and development of new drugs with improved therapeutic effects.
Used in Drug Discovery:
2-Bromothieno[2,3-b]pyridine has attracted significant interest in the field of drug discovery due to its unique structure and potential pharmacological properties. Researchers are exploring its use in the development of new drugs, particularly in the area of cancer treatment, where its incorporation into drug molecules may enhance their efficacy and selectivity.
Used in Medicinal Chemistry Research:
In medicinal chemistry, 2-Bromothieno[2,3-b]pyridine plays a crucial role in the study of molecular interactions and the design of new chemical entities. Its unique structural features provide a foundation for understanding the relationship between molecular structure and biological activity, ultimately contributing to the advancement of drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 72808-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,0 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72808-92:
(7*7)+(6*2)+(5*8)+(4*0)+(3*8)+(2*9)+(1*2)=145
145 % 10 = 5
So 72808-92-5 is a valid CAS Registry Number.

72808-92-5SDS

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 2-bromothieno[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names -

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:72808-92-5 SDS

72808-92-5Upstream product

72808-92-5Downstream Products

72808-92-5Relevant academic research and scientific papers

A Thieno[2,3-b]pyridine-Flanked Diketopyrrolopyrrole Polymer as an n-Type Polymer Semiconductor for All-Polymer Solar Cells and Organic Field-Effect Transistors

Chen, Hung-Yang,Nikolka, Mark,Wadsworth, Andrew,Yue, Wan,Onwubiko, Ada,Xiao, Mingfei,White, Andrew J. P.,Baran, Derya,Sirringhaus, Henning,McCulloch, Iain

, p. 71 - 79 (2018)

A novel fused heterocycle-flanked diketopyrrolopyrrole (DPP) monomer, thieno[2,3-b]pyridine diketopyrrolopyrrole (TPDPP), was designed and synthesized. When copolymerized with 3,4-difluorothiophene using Stille coupling polymerization, the new polymer pTPDPP-TF possesses a highly planar conjugated polymer backbone due to the fused thieno[2,3-b]pyridine flanking unit that effectively alleviates the steric hindrance with both the central DPP core and the 3,4-difluorothiophene repeat unit. This new polymer exhibits a high electron affinity (EA) of -4.1 eV and was successfully utilized as an n-type polymer semiconductor for applications in organic field-effect transistors (OFETs) and all polymer solar cells. A promising n-type charge carrier mobility of 0.1 cm2 V-1 s-1 was obtained in bottom-contact, top-gate OFETs, and a power conversion efficiency (PCE) of 2.72% with a high open-circuit voltage (VOC) of 1.04 V was achieved for all polymer solar cells using PTB7-Th as the polymer donor.

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