105995-16-2

Basic information

• Product Name: 2-Thienyl-carbamic Acid Ethyl Ester
• Synonyms: Carbamic acid, N-2-thienyl-, ethyl ester;ethyl thiophen-2-ylcarbamate;2-Thienyl-carbamic Acid Ethyl Ester
• CAS NO: 105995-16-2
• Molecular Formula: C₇H₉NO₂S
• Molecular Weight: 171.22
• Product Categories: Heterocycles
• Mol File: 105995-16-2.mol

Chemical Properties

• Boiling Point: 212 °C at 760 mmHg
• Flash Point: 82 °C
• Appearance: /
• Density: 1.269 g/cm³
• Vapor Pressure: 0.177mmHg at 25°C
• Refractive Index: 1.586
• CAS DataBase Reference: 2-Thienyl-carbamic Acid Ethyl Ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Thienyl-carbamic Acid Ethyl Ester(105995-16-2)
• EPA Substance Registry System: 2-Thienyl-carbamic Acid Ethyl Ester(105995-16-2)

Safety Data

• Hazardous Substances Data: 105995-16-2(Hazardous Substances Data)

Usage

Uses

Used in Pesticide Industry:
2-Thienyl-carbamic Acid Ethyl Ester is used as an insecticide for controlling a variety of pests. It functions by inhibiting the activity of acetylcholinesterase, an enzyme crucial for the nervous system in insects and pests. This disruption leads to paralysis and ultimately death of the targeted organisms, making it an effective tool in managing pest populations.
Used in Agricultural Applications:
In agriculture, 2-Thienyl-carbamic Acid Ethyl Ester is utilized as a pesticide to protect crops from damaging insects. Its ability to paralyze and kill pests helps in reducing crop losses and ensuring a healthy yield. This contributes to maintaining the quality and quantity of agricultural produce, thereby supporting food security and economic stability in the farming sector.

InChI:InChI=1/C7H9NO2S/c1-2-10-7(9)8-6-4-3-5-11-6/h3-5H,2H2,1H3,(H,8,9)

Upstream product

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Relevant articles and documents

New and simple synthesis of acid azides, ureas and carbamates from carboxylic acids: Application of peptide coupling agents EDC and HBTU

Conversion of carboxylic acids into acid azides using peptide coupling agents, EDC and HBTU is described. The procedure is efficient, practical and applicable to a diverse range of carboxylic acids including N-protected amino acids. Using the same reagents, one-pot synthesis of ureas, dipeptidyl urea esters and carbamates from acids has also been achieved. The Royal Society of Chemistry 2010.

Microwave-assisted intramolecular cyclization of electron-rich heterocycle derivatives by a palladium-catalyzed coupling reaction

Nitrogenated heteropolycyclic systems were obtained by intramolecular palladium-catalyzed coupling reactions promoted by microwave irradiation. Georg Thieme Verlag Stuttgart.

ARE THIOPHENES ATTACKED AT SULPHUR BY NITRENES?

Ethyl azidoformate is shown to attack a range of thiophenes at sulphur giving transient S,N-ylides which can be trapped with acenaphthylene as adducts; thiophene yields self-trapped products also.