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Bendiocarb

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Identification
Molecular formula
C11H13NO4
CAS number
22781-23-3
IUPAC name
(5,5-dimethyl-3-oxo-cyclohexen-1-yl) N,N-dimethylcarbamate
State
State

At room temperature, Bendiocarb typically exists as a solid. It may be found in this state in various formulated products designed for pesticidal use.

Melting point (Celsius)
129.00
Melting point (Kelvin)
402.00
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.00
General information
Molecular weight
223.27g/mol
Molar mass
223.2680g/mol
Density
1.2300g/cm3
Appearence

Bendiocarb is a colorless crystalline solid. It is often provided in various formulations including powder or liquid for commercial use in pest control.

Comment on solubility

Solubility of (5,5-dimethyl-3-oxo-cyclohexen-1-yl) N,N-dimethylcarbamate

The solubility of (5,5-dimethyl-3-oxo-cyclohexen-1-yl) N,N-dimethylcarbamate is influenced by various factors, particularly its structural characteristics and the polarity of its functional groups. Generally, this compound is expected to exhibit the following solubility traits:

  • Polar interactions: Due to the presence of the carbamate functional group, which can participate in hydrogen bonding, the compound may demonstrate a certain level of solubility in polar solvents like water.
  • Non-polar interactions: The cyclohexene portion of the molecule introduces non-polar characteristics. Therefore, it is likely to be more soluble in non-polar solvents such as hexane or toluene.
  • Saturation point: The solubility may also depend on temperature, with increased temperatures generally allowing for greater solubility in both polar and non-polar solvents.
  • pH sensitivity: The solubility may vary with changes in pH, as it could affect the ionization of the carbamate group.

In conclusion, while (5,5-dimethyl-3-oxo-cyclohexen-1-yl) N,N-dimethylcarbamate can dissolve in various solvents, careful consideration of the solvent type and environmental conditions will be essential for predicting its solubility behavior accurately.

Interesting facts

Interesting Facts about (5,5-Dimethyl-3-oxo-cyclohexen-1-yl) N,N-Dimethylcarbamate

(5,5-Dimethyl-3-oxo-cyclohexen-1-yl) N,N-dimethylcarbamate is a fascinating compound with unique properties and applications in the field of organic chemistry. Here are some intriguing points to consider:

  • Pesticide Development: This compound is primarily valued for its potential use in agriculture as a pesticide, showcasing its importance in enhancing crop yield and protecting against pests.
  • Structure and Stability: The cyclohexenyl structure provides significant stability, making the compound less reactive under standard conditions, which is critical for its shelf life and effectiveness.
  • Reaction Pathways: It can participate in various chemical reactions, including nucleophilic substitutions and decarbamoylation, which are essential for synthetic organic chemistry.
  • Therapeutic Potential: Some studies suggest that derivatives of carbamate compounds may possess biological activity, engendering interest in their role in medicinal chemistry and potential therapeutic uses.
  • Regulatory Aspects: As with many pesticides and herbicides, understanding the regulatory framework governing carbamate compounds is crucial for their safe application and environmental impact assessment.

The structural complexity and functional diversity of (5,5-dimethyl-3-oxo-cyclohexen-1-yl) N,N-dimethylcarbamate make it a noteworthy subject for chemists and researchers. As you delve deeper into its chemistry, remember:

"The study of compounds like these is not just about understanding their structure, but also about unlocking their potential for innovation."

Exploring the multifaceted nature of this compound opens doors to advancements in both agricultural practices and synthetic methodologies.

Synonyms
DIMETAN
122-15-6
Geigy 19258
5,5-Dimethyl-3-oxocyclohex-1-enyl dimethylcarbamate
UNII-215ZV6RPXL
EINECS 204-525-8
215ZV6RPXL
5,5-Dimethyl-3-oxo-1-cyclohexen-1-yl dimethylcarbamate
ENT 24,728
BRN 3280184
AI3-24728
DIMETAN [MI]
5,5-Dimethyldihydroresorcinol dimethylcarbamate
G 19258
Dimethylcarbamate de 5,5-dimethyl dihydroresorcinol [French]
DTXSID8041872
5,5-Dimethyl-dihydroresorcinol-N,N-dimethylcarbamat [German]
2-Cyclohexen-1-one, 3-hydroxy-5,5-dimethyl-, dimethylcarbamate
5,5-Dimethyl-4,5-dihydro-3-resorcyl-dimethyl-carbamat [German]
GEIGY-19,258
(5,5-Dimethyl-3-oxo-cyclohex-1-en-yl)-N,N-dimethyl-carbamaat [Dutch]
(5,5-Dimethyl-3-oxo-cyclohex-1-en-yl)-N,N-dimethyl-carbamat [German]
(5,5-Dimetil-3-oxo-cicloes-1-en-il)-N,N-dimetil-carbammato [Italian]
3-08-00-00048 (Beilstein Handbook Reference)
Carbamic acid, dimethyl-, 5,5-dimethyl-3-oxo-1-cyclohexen-1-yl ester
5,5-Dimethyl-dihydroresorcinol-N,N-dimethylcarbamat
Dimethylcarbamate de 5,5-dimethyl dihydroresorcinol
5,5-Dimethyl-3-oxo-1-cyklohexenylester kyseliny dimethylkarbaminove [Czech]
ENT-24,728
5,5-Dimethyl-4,5-dihydro-3-resorcyl-dimethyl-carbamat
(5,5-Dimethyl-3-oxo-cyclohex-1-en-yl)-N,N-dimethyl-carbamaat
(5,5-Dimethyl-3-oxo-cyclohex-1-en-yl)-N,N-dimethyl-carbamat
(5,5-Dimetil-3-oxo-cicloes-1-en-il)-N,N-dimetil-carbammato
5,5-Dimethyl-3-oxo-1-cyklohexenylester kyseliny dimethylkarbaminove
Carbamic acid, dimethyl-, 5,5-dimethyl-3-oxo-1-cyclohexene-1-yl ester
Carbamic acid, dimethyl-, ester with 3-hydroxy-5,5-dimethyl-2-cyclohexen-1-one
G-19258
CARBAMIC ACID, N,N-DIMETHYL-, 5,5-DIMETHYL-3-OXO-1-CYCLOHEXEN-1-YL ESTER
RefChem:134166
DTXCID6021872
5,5-dimethyl-3-oxocyclohex-1-en-1-yl N,N-dimethylcarbamate
Carbamic acid, dimethyl-, 5,5-dimethyl-3-oxo-1-cyclohexene-1-yl ester (9CI)
(5,5-dimethyl-3-oxocyclohexen-1-yl) N,N-dimethylcarbamate
SCHEMBL119630
ITEQSCBLCCNACE-UHFFFAOYSA-N
NS00023980
Q27253523