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Chloralose

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Identification
Molecular formula
C9H16ClNOS2
CAS number
53404-96-5
IUPAC name
2-chloroallyl N,N-diethylcarbamodithioate
State
State

This compound is a liquid at room temperature.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
239.85g/mol
Molar mass
239.8510g/mol
Density
1.1575g/cm3
Appearence

2-chloroallyl N,N-diethylcarbamodithioate appears as a colorless to pale yellow viscous liquid.

Comment on solubility

Solubility of 2-chloroallyl N,N-diethylcarbamodithioate

The solubility of 2-chloroallyl N,N-diethylcarbamodithioate is influenced by its unique chemical structure and nature of interactions within a solvent. This compound demonstrates varying solubility in different solvents, notably:

  • Polar solvents: Generally, compounds with polar functional groups tend to dissolve well in polar solvents. However, the presence of the chlorine atom may influence the overall polar characteristics.
  • Non-polar solvents: Given its organic nature, 2-chloroallyl N,N-diethylcarbamodithioate often shows increased solubility in non-polar solvents, showcasing greater compatibility in apolar environments.
  • Water solubility: The solubility in water is usually limited due to the non-polar characteristics of the alkyl chains present in the molecule.

Factors that may dictate the actual solubility of this compound include:

  1. Temperature: As temperature increases, solubility can also increase.
  2. Presence of other solutes: Certain solutes can enhance or inhibit solubility.
  3. pH levels: Changes in pH can affect solubility, particularly for compounds that may interact with hydronium or hydroxide ions.

In summary, the solubility of 2-chloroallyl N,N-diethylcarbamodithioate is a complex interplay of its molecular properties and the solvent characteristics. Understanding these interactions is crucial for its application in various chemical processes.

Interesting facts

Interesting Facts about 2-Chloroallyl N,N-Diethylcarbamodithioate

2-Chloroallyl N,N-diethylcarbamodithioate is a compound rich in intriguing properties and applications, drawing interest from scientists and researchers alike. This compound can be explored in various aspects, making it a fascinating subject of study in the field of chemistry.

Chemical Structure and Properties

The unique structure of 2-chloroallyl N,N-diethylcarbamodithioate includes:

  • Functional Groups: It contains both thiocarbonyl and alkylamine functional groups, which can significantly influence its reactivity.
  • Chlorine Substitution: The presence of a chlorine atom increases the electrophilic character of the compound, enhancing its potential as a reactive agent.

Applications in Agriculture

This compound has garnered attention for its potential use in agriculture:

  • Pesticide Development: Due to its unique structure, it may serve as an active ingredient in the formulation of pesticides.
  • Plant Health: Research suggests it could be effective in protecting crops from particular pests and diseases, promoting sustainable agricultural practices.

Toxicity and Safety

Like many chemical compounds, safety is a crucial consideration:

  • Handling Precautions: It is essential to observe safety protocols while handling this compound to mitigate any potential toxicity.
  • Environmental Impact: Studies on its biodegradability and environmental effects are ongoing to ensure its safe use in real-world applications.

In Summary

2-Chloroallyl N,N-diethylcarbamodithioate is a prime example of a compound that bridges the gaps between organic chemistry and practical applications in agriculture. As scientists continue to explore its potentials, we may witness significant advancements in pest control strategies and sustainable farming.

As noted in scientific discussions, "The future of agriculture lies in the skilled use of chemistry to create safer and more effective solutions." This compound represents a step in that direction!

Synonyms
SULFALLATE
Vegadex
95-06-7
Thioallate
CDEC
Vegadex super
2-Chloroallyl diethyldithiocarbamate
Vegedex
Chlorallyl diethyldithiocarbamate
Caswell No. 180
NCI-C00453
2-Chlorallyl diethyldithiocarbamate
2-Chloroallyl N,N-diethyldithiocarbamate
Sulfallate [ISO:BSI]
CP 4572
CP 4,742
Carbamodithioic acid, diethyl-, 2-chloro-2-propenyl ester
CCRIS 566
NSC 16085
Diethyldithiocarbamic acid 2-chloroallyl ester
HSDB 1538
2-Chloro-2-propenyl diethylcarbamodithioate
EINECS 202-388-9
EPA Pesticide Chemical Code 039001
UNII-7U7BI7173J
BRN 1772271
2-Chloro-2-propene-1-thiol diethyldithiocarbamate
Carbamic acid, diethyldithio-, 2-chloroallyl ester
DTXSID7021289
2-Propene-1-thiol, 2-chloro-, diethyldithiocarbamate
Diethylcarbamodithioic acid 2-chloro-2-propenyl ester
7U7BI7173J
SULFALLATE [MI]
SULFALLATE [ISO]
2-chloroprop-2-enyl N,N-diethylcarbamodithioate
NSC-16085
SULFALLATE [HSDB]
SULFALLATE [IARC]
DTXCID501289
2-chloroprop-2-en-1-yl diethyldithiocarbamate
CHEBI:82218
4-04-00-00395 (Beilstein Handbook Reference)
N,N-Diethyldithiocarbamic acid 2-chloroallyl ester
NSC16085
CP-4742
SULFALLATE (IARC)
2-CHLOROALLYL DIETHYL(DITHIOCARBAMATE)
2-CHLORO-2-PROPEN-1-YL N,N-DIETHYLCARBAMODITHIOATE
Vegadex 4EC
Vegadex 20G
Sulphallate
N,N-diethyl((2-chloroprop-2-en-1-yl)sulfanyl)carbothioamide
N,N-diethyl[(2-chloroprop-2-en-1-yl)sulfanyl]carbothioamide
Sulphallic acid
Sulfallic acid
MLS002152939
SCHEMBL136254
CHEMBL538146
NCI CO0453
WLN: 2N2&YUS&S1YGU1
2Chlorallyl diethyldithiocarbamate
carbamodithioic acid, diethyl-, 2-chloro-2-propanyl ester
2Chloroallyl diethyldithiocarbamate
HMS3039C15
Carbamic acid, 2-chloroallyl ester
Tox21_200042
2Chloroallyl N,Ndiethyldithiocarbamate
2Chloro2propenyl diethylcarbamodithioate
CP 4742
CAS-95-06-7
USEPA/OPP Pesticide Code: 039001
NCGC00090829-01
NCGC00090829-02
NCGC00257596-01
2-Propene-1-thiol, diethyldithiocarbamate
SMR001224534
2-Chloro-2-propenyl diethyldithiocarbamate
2Chloro2propene1thiol diethyldithiocarbamate
DB-057551
2-Chloro-2-propenyl diethyldithiocarbamate #
Diethyldithiocarbamic acid 2chloroallyl ester
NS00015291
Sulfallate, PESTANAL(R), analytical standard
2Propene1thiol, 2chloro, diethyldithiocarbamate
C19096
Carbamic acid, diethyldithio, 2chloroallyl ester
Carbamodithioic acid, 2-chloro-2-propenyl ester
N,NDiethyldithiocarbamic acid 2chloroallyl ester
Diethylcarbamodithioic acid 2chloro2propenyl ester
Carbamodithioic acid, diethyl, 2chloro2propenyl ester
Q27155815
Z18907240
202-388-9