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Cycloate

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Identification
Molecular formula
C11H21NOS
CAS number
1134-23-2
IUPAC name
S-ethyl N-cyclohexyl-N-ethyl-carbamothioate
State
State
Cycloate is a liquid at room temperature. It is often used in its liquid form due to its effectiveness and ease of application in herbicidal functions.
Melting point (Celsius)
-28.00
Melting point (Kelvin)
245.15
Boiling point (Celsius)
282.00
Boiling point (Kelvin)
555.15
General information
Molecular weight
215.37g/mol
Molar mass
215.3750g/mol
Density
1.0255g/cm3
Appearence

Cycloate is a colorless to pale yellow liquid. It is known for its oily texture and typically appears clear but might exhibit slight turbidity when impure.

Comment on solubility

Solubility of S-ethyl N-cyclohexyl-N-ethyl-carbamothioate

S-ethyl N-cyclohexyl-N-ethyl-carbamothioate exhibits a unique solubility profile, which can be influenced by its chemical structure. Understanding this solubility is essential for its applications and behavior in various environments.

Key Characteristics of Solubility:

  • Solvent Dependence: S-ethyl N-cyclohexyl-N-ethyl-carbamothioate tends to be soluble in organic solvents due to its non-polar hydrocarbon components. Common solvents include:
    • Chloroform
    • Ethyl acetate
    • Toluene
  • Water Solubility: Its solubility in water is generally low, which is typical for many carbamothioate compounds. This limited solubility can be attributed to:
    • The large cyclohexyl and ethyl groups that hinder interaction with water molecules.
    • The overall non-polar characteristics of the compound.
  • pH Sensitivity: The solubility may also be affected by pH levels, showing changes in solubility when entering more acidic or basic conditions.

In summary, while S-ethyl N-cyclohexyl-N-ethyl-carbamothioate is soluble in various organic solvents, its limited water solubility reflects the compound's structure and necessitates careful consideration in applications where aqueous environments are involved. As the saying goes, "Like dissolves like," and in this case, the compound's affinity for non-polar solvents is well demonstrated.

Interesting facts

Interesting Facts about S-ethyl N-cyclohexyl-N-ethyl-carbamothioate

S-ethyl N-cyclohexyl-N-ethyl-carbamothioate is a compound that finds its applications predominantly in the field of agriculture as a pesticide. Here are some remarkable insights into this intriguing chemical:

  • Functional Role: It acts primarily as a thiocarbamate, a class of pesticides that are known for their effectiveness against various pests while being less harmful to non-target organisms.
  • Mechanism of Action: The compound interferes with the enzyme systems involved in the nervous function of insects, leading to pest control while minimizing environmental risks.
  • Synthetic Pathway: The synthesis of this compound involves a series of chemical reactions, typically engaging in nucleophilic substitutions and the formation of thiocarbamate linkages.
  • Field Applications: S-ethyl N-cyclohexyl-N-ethyl-carbamothioate has been utilized effectively in various agricultural settings, helping to protect crops from nematodes and other agricultural pests.
  • Environmental Impact: One of the compelling factors for its use is its relatively low toxicity to mammals and potential for rapid degradation in the environment, making it a suitable choice among modern agrochemicals.

The ongoing research into compounds such as S-ethyl N-cyclohexyl-N-ethyl-carbamothioate underscores the importance of developing effective pest management strategies that align with sustainable agricultural practices. As we explore the interactions of such compounds further, the balance between efficacy and environmental safety becomes a pivotal consideration in agricultural chemistry.

Synonyms
CYCLOATE
1134-23-2
Etsan
Ro-Neet
Eurex
Ronit
Sabet
Hexylthiocarbam
Ro-Neet E
Ro-Neet 10G
Ro-Neet 6-E
Caswell No. 432A
Cycloate [BSI:ISO]
Cycloate [ISO]
S-Ethyl N-cyclohexylthiocarbamate
R 2063
S-Ethyl N-ethylcyclohexanecarbamothioate
HSDB 1712
S-Ethylethylcyclohexylthiocarbamate
S-Ethyl N-cyclohexyl-N-ethylthiocarbamate
Carbamothioic acid, cyclohexylethyl-, S-ethyl ester
S-Ethyl cyclohexylethylthiocarbamate
UNII-IMZ37NA07H
S-Ethyl cyclohexylethylcarbamothioate
EINECS 214-482-7
IMZ37NA07H
Carbamothioic acid, N-cyclohexyl-N-ethyl-, S-ethyl ester
R-2063
EPA Pesticide Chemical Code 041301
S-Ethyl N-ethylthiocyclohexanecarbamate
BRN 2937178
CCRIS 9270
Ro-Neet 6E
Carbamic acid, cyclohexylethylthio-, S-ethyl ester
DTXSID6032356
S-ethyl N-cyclohexyl-N-ethylcarbamothioate
S-Ethyl N-ethyl N-cyclohexylthiolcarbamate
S-Ethyl N-ethyl-N-cyclohexylthiolcarbamate
Cyclohexanecarbamic acid, N-ethylthio-, S-ethyl ester
S-Ethyl N-cyclohexyl-N-ethyl(thiocarbamate)
CYCLOATE [HSDB]
S-ethyl cyclohexyl(ethyl)thiocarbamate
DTXCID4012356
Ethyl cyclohexylethylthiocarbamate
S-Ethyl (cyclohexyl)ethylthiocarbamate
S-Ethyl N-ethyl-N-cyclohexylthiocarbamate
cycleate
ethsane
Roneet
cycloic acid
S-ethyl-N-cyclohexylthiocarbamate
RoNeet E
RoNeet 6E
RoNeet 10G
S-Ethyl cyclohexylethylcarbamothioate (8CI)
S-Ethyl cyclohexylethylcarbamothioate (8CI)(9CI)
SEthylethylcyclohexylthiocarbamate
SEthyl cyclohexylethylthiocarbamate
SEthyl Nethylthiocyclohexanecarbamate
SEthyl Nethylcyclohexanecarbamothioate
SEthyl NethylNcyclohexylthiolcarbamate
S-ethyl cyclohexylethyl carbamothioate
SEthyl Nethyl Ncyclohexylthiolcarbamate
SEthyl NcyclohexylNethyl(thiocarbamate)
USEPA/OPP Pesticide Code: 041301
SEthyl cyclohexylethylcarbamothioate (8CI)
N-cyclohexyl-N-ethyl(ethylsulfanyl)formamide
R2063
Carbamic acid, cyclohexylethylthio, Sethyl ester
Carbamothioic acid, cyclohexylethyl, Sethyl ester
SEthyl cyclohexylethylcarbamothioate (8CI)(9CI)
Cyclohexanecarbamic acid, Nethylthio, Sethyl ester
dfcafrgabixsds-uhfffaoysa-n
S-Ethyl cyclohexyl(ethyl)carbamothioate
CHEBI:81955
SCHEMBL42572
CHEMBL1889969
Tox21_300884
AKOS015898605
NCGC00168298-01
NCGC00168298-02
NCGC00254788-01
CAS-1134-23-2
S-Ethyl N-ethyl-N-cyclohexyl-thiocarbamate
Cycloate, PESTANAL(R), analytical standard
NS00001141
C18780
Q1147426