S-Ethyl cyclohexyl(ethyl)carbamothioate

Basic Information

View in Editor

CAS Number

1134-23-2

Molecular Formula

C11H21NOS

Molecular Weight

215.36 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Fine Chemicals Surfactants Anionic Surfactants

Basic Physical Properties

Melting Point

11.5°C

Boiling Point

303 °C at 760 mmHg

Refractive Index

1.5500 (estimate)

SMILES

View in Editor

CCN(C1CCCCC1)C(=O)SCC

InChI

InChI=1S/C11H21NOS/c1-3-12(11(13)14-4-2)10-8-6-5-7-9-10/h10H,3-9H2,1-2H3

InChIKey

DFCAFRGABIXSDS-UHFFFAOYSA-N

LogP

3.5141000000000027

Topological Polar Surface Area

20.310000000000002 Å²

Hydrogen Bond Donor/Acceptor

0 / 2

Complexity

178

Safety Information

View Safety Information

GHS Hazard Pictograms

H302

Hazard Statement

H302 Harmful if swallowed
Acute toxicity, oral

Synonyms & References

English

cycloate
S-ethyl N-cyclohexyl-N-ethylthiocarbamate
Cycloate Solution
Cycloate Standard
S-ethyl N-cyclohexyl-N-ethylcarbamothioate
Caswell No. 432A
Etsan
Eurex
Hexylthiocarbam
Ro-Neet
Ro-Neet E
Ronit
Sabet
S-ethyl cyclohexyl(ethyl)carbamothioate
S-ethyl cyclohexyl(ethyl)thiocarbamate
S-ethyl cyclohexylethylcarbamothioate
S-ethyl ethylcyclohexylthiocarbamate
S-ethyl N-ethylthiocyclohexanecarbamate
S-ethyl-N-ethyl-N-cyclohexylthiolcarbamate
S-Ethyl N-cyclohexyl-N-ethylthiocarbamate

MDL Number

MFCD00055341

Customs Code

2930909090

FAQ

What are the physical and chemical properties of S-Ethyl cyclohexyl(ethyl)carbamothioate (CAS: 1134-23-2)?

S-Ethyl cyclohexyl(ethyl)carbamothioate is a crystalline compound with a molecular weight of approximately 242.27 g/mol. It has a low solubility in water but is soluble in organic solvents like ethanol and acetone. The compound is moderately reactive, especially towards nucleophiles and reducing agents. It is stable under normal storage conditions but should be protected from strong oxidizers and heat.

How is S-Ethyl cyclohexyl(ethyl)carbamothioate (CAS: 1134-23-2) typically synthesized?

S-Ethyl cyclohexyl(ethyl)carbamothioate can be synthesized via an amide carbamation process, where cyclohexylamine reacts with ethyl isothiocyanate in the presence of a base such as pyridine. The reaction is typically carried out at room temperature, and the yield can be up to 80%. The process requires mild conditions and can be optimized for better selectivity and higher yields.

What industries use S-Ethyl cyclohexyl(ethyl)carbamothioate (CAS: 1134-23-2)?

S-Ethyl cyclohexyl(ethyl)carbamothioate finds applications in various industries. It is used in the pharmaceutical sector for its potential as a pesticide and fungicide. In the polymer industry, it can serve as a stabilizer. Additionally, it can be used in the electronics industry as a component in sensors and semiconductors.

What precautions should be taken when handling S-Ethyl cyclohexyl(ethyl)carbamothioate (CAS: 1134-23-2)?

When handling S-Ethyl cyclohexyl(ethyl)carbamothioate, it is important to use appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Work should be conducted in a fume hood to minimize inhalation risks. Spills should be cleaned up using appropriate absorbent materials, and the area should be well-ventilated. Always consult the Safety Data Sheet (SDS) for detailed handling instructions and emergency procedures.