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(2,4-dinitrophenyl) N,N-dimethylcarbamodithioate

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Identification
Molecular formula
C10H10N4O4S2
CAS number
1522-92-5
IUPAC name
(2,4-dinitrophenyl) N,N-dimethylcarbamodithioate
State
State

At room temperature, (2,4-dinitrophenyl) N,N-dimethylcarbamodithioate is a solid. Its stability as a solid makes it convenient to handle in laboratory settings. The compound's crystalline nature is also reflective of its organized internal structure.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
287.32g/mol
Molar mass
287.3120g/mol
Density
1.4500g/cm3
Appearence

(2,4-dinitrophenyl) N,N-dimethylcarbamodithioate typically appears as a yellow crystalline solid. It is characterized by its bright color, which is due to the dinitrophenyl group present in the compound. The compound is generally used in organic chemistry for various applications, including as an intermediate in chemical synthesis.

Comment on solubility

Solubility of (2,4-dinitrophenyl) N,N-dimethylcarbamodithioate

The solubility of (2,4-dinitrophenyl) N,N-dimethylcarbamodithioate can be influenced by several key factors:

  • Polarity: The presence of both hydrophilic (water-attracting) and hydrophobic (water-repelling) groups in the molecular structure plays a crucial role.
  • Temperature: Solubility often increases with temperature, making solvents at varying temperatures essential to consider.
  • Solvent type: This compound may show varying degrees of solubility in different solvents, such as organic or aqueous environments.

It is essential to recognize that similar compounds might have differing solubility characteristics, and thus, laboratory testing is often required to precisely determine solubility levels. As a general rule, the more polar a compound is, the better it dissolves in polar solvents, while nonpolar compounds dissolve better in nonpolar solvents.

In summary, understanding the solubility of (2,4-dinitrophenyl) N,N-dimethylcarbamodithioate entails considering multiple factors, and experimentation remains the best approach to fully appreciate its solubility behavior.

Interesting facts

Interesting Facts about (2,4-Dinitrophenyl) N,N-Dimethylcarbamodithioate

(2,4-Dinitrophenyl) N,N-dimethylcarbamodithioate, often abbreviated as DNDMCD, is a fascinating compound that has attracted the attention of chemists due to its unique properties and applications. Here are some intriguing highlights:

  • Pesticide Properties: DNDMCD has been primarily studied for its use as a pesticide, particularly in agricultural settings. Its structure allows it to act effectively against a variety of pests, making it a useful compound for crop protection.
  • Functional Group Diversity: The presence of the dinitrophenyl group in this molecule offers distinct electronic characteristics, influencing the reactivity and efficacy of the compound. The combination of electron-withdrawing and donating groups can enhance its biological activity.
  • Synthesis and Reactions: The synthesis of DNDMCD involves a series of chemical reactions that highlight the versatility of thiourea derivatives in organic synthesis. This allows for the further exploration of thiocompounds in various chemical pathways.
  • Research Significance: Studies have shown that compounds like DNDMCD can serve as models for understanding nerve agents and their mechanisms. As a result, it has implications in both agricultural and toxicological research.
  • Environmental Impact: While effective, the breakdown products of DNDMCD and its fate in the environment are crucial aspects of study. Being aware of its persistence and degradation in natural systems helps in assessing ecological risks.

While DNDMCD serves important functions, it also exemplifies the need for careful handling and in-depth understanding of chemical compounds to balance their beneficial uses with safety and environmental considerations. As we delve deeper into the characteristics of such compounds, we can continue to innovate while minimizing risks.

Synonyms
89-37-2
USAF SN-31
2,4-Dinitrophenyl dimethyldithiocarbamate
Carbamodithioic acid, dimethyl-, 2,4-dinitrophenyl ester
(2,4-dinitrophenyl) N,N-dimethylcarbamodithioate
YSU5XGX97F
2,4-Dinitrophenyl-dimethyl-dithiocarbamate
NSC-11461
DTXSID0058986
Carbamodithioic acid, N,N-dimethyl-, 2,4-dinitrophenyl ester
4-06-00-01760 (Beilstein Handbook Reference)
CARBAMIC ACID, DIMETHYLDITHIO-, 2,4-DINITROPHENYL ESTER
EINECS 201-902-9
NSC 11461
BRN 2475355
AI3-28653
UNII-YSU5XGX97F
Dimethyldithiocarbamic acid, 2,4-dinitrophenyl ester
DTXCID8048654
SCHEMBL11760073
AIWZJEMZVHJAQB-UHFFFAOYSA-N
WLN: WNR CNW DSYUS&N1&1
NSC11461
AKOS024383899
2,4-Dinitrophenyl-dimethyldithio-carbamate
DS-003608
NS00039326
Carbamodithioic acid, 2,4-dinitrophenyl ester
201-902-9