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Selenophene-2-carbonitrile is a heterocyclic chemical compound with the molecular formula C5H3NSe. It features a selenophene ring fused with a carbonitrile group, which endows it with unique structural and electronic properties. selenophene-2-carbonitrile is recognized for its potential in various fields, including organic synthesis, materials science, and medicinal chemistry, where it can be utilized as a building block for creating other organic compounds, polymers, and pharmaceuticals.

7651-60-7

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7651-60-7 Usage

Uses

Used in Organic Synthesis:
Selenophene-2-carbonitrile is used as a building block in organic synthesis for the creation of other organic compounds and polymers. Its unique structure allows for the development of materials with specific properties, such as semiconducting and optoelectronic materials, which are crucial for various technological applications.
Used in Materials Science:
In the field of materials science, selenophene-2-carbonitrile is utilized as a precursor for synthesizing advanced materials with tailored electronic and optical characteristics. Its incorporation into polymers can lead to the production of materials suitable for use in electronic devices and optoelectronic systems.
Used in Medicinal Chemistry:
Selenophene-2-carbonitrile has garnered interest in medicinal chemistry as a potential pharmaceutical agent. Its chemical structure and reactivity make it a valuable component in the design and synthesis of new drugs and bioactive compounds, which could be used for treating various diseases and medical conditions.
Used in Pharmaceutical Development:
As a component in pharmaceutical development, selenophene-2-carbonitrile is employed for its potential to contribute to the discovery and creation of novel therapeutic agents. Its unique properties may offer advantages in drug design, potentially leading to more effective and targeted treatments.
However, it is important to note that selenophene-2-carbonitrile should be handled with caution due to its toxic and potentially hazardous nature. Proper safety measures and protocols must be followed to mitigate any risks associated with its use in research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7651-60-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,5 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7651-60:
(6*7)+(5*6)+(4*5)+(3*1)+(2*6)+(1*0)=107
107 % 10 = 7
So 7651-60-7 is a valid CAS Registry Number.

7651-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name selenophene-2-carbonitrile

1.2 Other means of identification

Product number -
Other names Selenophen-2-carbonitril

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:7651-60-7 SDS

7651-60-7Relevant academic research and scientific papers

Engineering aromatic heterocycle strategy: Improving copper electrodeposition performance via tuning the bandgap of diketopyrrolopyrrole-based leveler

Wang, Kang,Feng, Jinming,Xu, Jie,Li, Jun,Mai, Maria,Wang, Xiaomin,Wang, Limin

, (2020)

The bandgap of organics is an important descriptor to evaluate the interface adhesion of an organic agent on metal surface. However, insight into the role of chalcogens tuning of π-conjugated materials in influencing the bandgap is still deficient. Here, a family of diketopyrrolopyrrole(DPP)-based quaternary ammonium salts containing different chalcogens are innovatively synthesized through bottom-up strategy and served as new levelers in conformal copper electrodeposition. The photophysical and electrochemical properties including cyclic voltammetry (CV),potentiodynamic polarization curves and galvanostatic measurements (GMs) of those compounds were tested. Compared with other counterparts, SeDPP-QAS presents the narrowest bandgap showing great potential in conformal copper electrodeposition. Through-hole electroplating test and the scanning electron microscope (SEM) images of coating layer demonstrate that bandgap tuning is an efficient method to level and regulate the electrodeposition performance. Besides, theoretical calculations and X-ray photoelectron spectroscopy (XPS) were applied detect the adsorption mechanism between organic agent and copper surface. This work broadens the understanding of bandgap engineering of organics in copper electrodeposition, and provides guidance for the future design of organic materials in adsorbing other metal-based materials.

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