Taiy Chemical
2-(2-Aminoethyl)thiophene
Product Name Thiophene-2-ethylamine
Synonyms:17807 2-Thiophene ethylamine; THIOPHENE ETHYLAMINE; Thiophene-2-ethylamine HCL SALT; RARECHEM AL BW 0099; 2-(2'-THIENYL)ETHYL AMINE; 2-(2-THIENYL)ETHYLAMINE; 2-(2-THIENYL)-1-ETHANAMINE; 2-(2-Aminoethyl)thiophene; 2-(thiophen-2-yl)ethanamine; 2-thiophen-2-ylethanaminium; 2-(2'-Thienyl)Ethylamine; 2-Thiopheneethylamine; 2-Thiophenethylamine
CAS RN. 30433-91-1
EINECS 250-196-9
Molecular Weight 128.2148
Molecular Formula C6H10NS
Boiling Point(℃) 199.7°C at 760 mmHg
Flash Point(℃) 74.6°C
Hazard Symbols Xi Details
Xi
Risk Codes  R36/37/38;    Details
 R36/37/38;     Details
Safety Description  S26;S37/39;Details
 S26;S37/39; Details
FAQ
What is 2-(2-Aminoethyl)thiophene and how is it used in the industry?

2-(2-Aminoethyl)thiophene is a chemical compound that is commonly used in the pharmaceutical industry for its versatile applications. This compound is used as a building block for the synthesis of various drugs, such as anti-cancer agents, anti-inflammatory drugs, and antimicrobial agents. Additionally, it is utilized in the production of electronic materials and organic semiconductors due to its unique electronic properties.

What are the key benefits of using 2-(2-Aminoethyl)thiophene in pharmaceutical applications?

One of the main benefits of using 2-(2-Aminoethyl)thiophene in pharmaceutical applications is its ability to serve as a precursor for the synthesis of biologically active compounds. This compound provides a convenient starting material for the construction of complex molecules with desired pharmacological properties. Additionally, the presence of the amino group in the molecule allows for further functionalization, leading to the development of novel drug candidates.

How is 2-(2-Aminoethyl)thiophene synthesized and what are the common methods for its production?

2-(2-Aminoethyl)thiophene can be synthesized through various methods, with one of the most common routes being the reaction of ethylenediamine and thiophene-2-carboxaldehyde. This reaction leads to the formation of the desired compound with high selectivity and yield. Other methods for the production of 2-(2-Aminoethyl)thiophene include the reductive amination of 2-acetylthiophene or the direct amination of thiophene.

What are the potential applications of 2-(2-Aminoethyl)thiophene in the field of organic electronics?

In the field of organic electronics, 2-(2-Aminoethyl)thiophene demonstrates promising applications due to its electron-deficient nature and high charge carrier mobility. This compound can be incorporated into organic semiconductors, such as field-effect transistors and light-emitting diodes, to enhance their performance. The modification of the thiophene ring with the aminoethyl group further allows for tuning of the electronic properties, leading to improved device efficiency and stability.

What are the safety considerations associated with handling and working with 2-(2-Aminoethyl)thiophene in research and industrial settings?

When working with 2-(2-Aminoethyl)thiophene, it is important to adhere to proper safety measures to prevent any potential hazards. This compound should be handled in a well-ventilated area, and personal protective equipment, such as gloves and goggles, should be worn to avoid skin contact and eye irritation. Additionally, 2-(2-Aminoethyl)thiophene should be stored in a cool, dry place away from heat and sources of ignition to prevent decomposition. It is recommended to consult the material safety data sheet (MSDS) for specific guidelines on the safe handling and disposal of this compound.
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