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2,4-dichlorobenzo[4,5]thieno[2,3-d]pyrimidine is a heterocyclic chemical compound characterized by its complex molecular structure. It features a fused thieno and pyrimidine ring system, with two chlorine atoms attached to the benzene ring, contributing to its dichloro designation. 2,4-dichlorobenzo[4,5]thieno[2,3-d]pyrimidine is highly conjugated and aromatic, making it a versatile building block in various research and industrial applications.

76872-40-7

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76872-40-7 Usage

Uses

Used in Pharmaceutical Synthesis:
2,4-dichlorobenzo[4,5]thieno[2,3-d]pyrimidine is used as a key intermediate in the synthesis of pharmaceuticals for its unique structural properties. Its ability to be incorporated into drug molecules aids in the development of new therapeutic agents with potential applications in treating various diseases and conditions.
Used in Agrochemical Development:
In the agrochemical industry, 2,4-dichlorobenzo[4,5]thieno[2,3-d]pyrimidine is utilized as a precursor in the creation of novel agrochemicals. Its structural attributes allow for the design of compounds with specific pesticidal or herbicidal properties, contributing to more effective crop protection strategies.
Used in Materials Science:
2,4-dichlorobenzo[4,5]thieno[2,3-d]pyrimidine is employed in materials science for its potential to form new materials with unique electronic, optical, or mechanical properties. Its incorporation into polymers or other materials can lead to advancements in areas such as electronics, photonics, or nanotechnology.
Used in Biological Research:
Due to its distinctive molecular structure, 2,4-dichlorobenzo[4,5]thieno[2,3-d]pyrimidine is being investigated for potential biological activities and therapeutic uses. Its interactions with biological systems are of interest to researchers seeking to understand its effects and explore its possible applications in medicine and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 76872-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,7 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76872-40:
(7*7)+(6*6)+(5*8)+(4*7)+(3*2)+(2*4)+(1*0)=167
167 % 10 = 7
So 76872-40-7 is a valid CAS Registry Number.

76872-40-7Downstream Products

76872-40-7Relevant academic research and scientific papers

COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY APPARATUS

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Paragraph 0147; 0148; 0150, (2018/08/30)

PROBLEM TO BE SOLVED: To provide: a compound for an organic optoelectronic device capable of realizing an organic optoelectronic device having high efficiency and a long life span; an organic optoelectronic device employing the compound for an organic optoelectronic device; and a display apparatus including the organic optoelectronic device. SOLUTION: A compound for an organic optoelectronic device is represented by the specified chemical formula I. The chemical formula I and descriptions of each symbol in the formula are as defined herein. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2016,JPO&INPIT

CONDENSED CYCLIC COMPOUND, AND ORGANIC LIGHT EMITTING DEVICE INCLUDING THE SAME

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Paragraph 1432; 1436-1438, (2016/10/08)

Disclosed are a condensed ring compound and an organic light emitting device comprising the condensed ring compound. The organic light emitting device comprises: a first electrode; a second electrode facing the first electrode; and an organic layer interposed between the first electrode and the second electrode, wherein the organic layer comprises the condensed ring compound.COPYRIGHT KIPO 2015

Cyclic Guanidines. 14. Imidazothienopyrimidin-2-one Derivatives as Blood Platelet Aggregation Inhibitors

Ishikawa, Fumiyoshi,Kosasayama, Akira,Yamaguchi, Hitoshi,Watanabe, Yoshifumi,Saegusa, Junji,et al.

, p. 376 - 382 (2007/10/02)

A series of novel 1,2,3,5-tetrahydroimidazothieno-, --, and -pyrimidin-2-one derivatives has been prepared and tested for the activity of inhibiting platelet aggregation in rats in vitro and ex vivo.These compounds were synthes

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