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Fenobucarb

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Identification
Molecular formula
C11H15NO2
CAS number
3766-81-2
IUPAC name
(2-isopropoxyphenyl) N-methylcarbamate
State
State

At room temperature, Fenobucarb is a liquid. It is typically used in agricultural applications as a liquid formulation.

Melting point (Celsius)
-10.40
Melting point (Kelvin)
262.75
Boiling point (Celsius)
142.00
Boiling point (Kelvin)
415.15
General information
Molecular weight
193.24g/mol
Molar mass
193.2370g/mol
Density
1.0660g/cm3
Appearence

Fenobucarb appears as a colorless to pale yellow liquid. It is commonly used as an insecticide and may have a mild aromatic odor.

Comment on solubility

Solubility of (2-isopropoxyphenyl) N-methylcarbamate

The solubility of (2-isopropoxyphenyl) N-methylcarbamate, with the chemical formula C11H15NO2, is an intriguing aspect of its chemical characterization. Understanding the solubility behavior of this compound can provide valuable insights into its applications and functionality.

General Solubility Behavior

  • This compound is generally expected to exhibit moderate solubility in organic solvents such as ethanol and acetone.
  • Its solubility in water may be quite limited due to the hydrophobic nature of the isopropoxy group.
  • Solubility can also be influenced by factors such as temperature and pH, making it essential to consider environmental conditions when assessing its solubility.

Factors Affecting Solubility

Several factors are crucial in determining the solubility of (2-isopropoxyphenyl) N-methylcarbamate:

  • Polarity: The balance between the polar and non-polar characteristics of the molecule can greatly impact its solubility in different solvents.
  • Molecular Interactions: Hydrogen bonding and van der Waals forces play a role in solubility, particularly in the presence of polar solvents.

In summary, while (2-isopropoxyphenyl) N-methylcarbamate may not be highly soluble in aqueous solutions, its solubility in various organic solvents opens pathways for its use in diverse chemical applications. Understanding these characteristics can aid researchers and chemists in the effective utilization of this compound.

Interesting facts

Interesting Facts about (2-isopropoxyphenyl) N-methylcarbamate

(2-isopropoxyphenyl) N-methylcarbamate, often referred to in the scientific community for its unique properties, represents an intriguing class of chemicals known as carbamates. Here are some fascinating insights:

  • Functionality: This compound functions as an effective insecticide and herbicide, showcasing the broader importance of carbamates in agriculture.
  • Mechanism of Action: Its efficacy is primarily due to its ability to inhibit acetylcholinesterase, an essential enzyme for the nervous system in pests, leading to their eventual death.
  • Synthesis: The synthesis of (2-isopropoxyphenyl) N-methylcarbamate involves a reaction between a phenolic compound and a carbamate precursor, illustrating the elegance of organic synthesis.
  • Research Significance: Numerous studies have highlighted its potential in pest control, making it a subject of interest in both entomology and toxicology research.
  • Applications: Beyond agriculture, it may also find applications in the pharmaceutical industry for developing new anticholinergic agents.

In summary, (2-isopropoxyphenyl) N-methylcarbamate is not just a chemical compound; it’s a prime example of how chemistry intertwines with agricultural science and environmental management. As one might say, “In every molecule, there's a story waiting to be uncovered!”

Synonyms
propoxur
114-26-1
Baygon
2-Isopropoxyphenyl methylcarbamate
Aprocarb
Propoxure
Sendran
Propoxylor
Blattanex
Blattosep
Mrowkozol
Propotox
Suncide
Bolfo
Boruho
Brygou
2-Isopropoxyphenyl N-methylcarbamate
Dalf dust
Invisi-Gard
Arprocarb
Isocarb
Propyon
Rhoden
Bifex
Boruho 50
IPMC
o-Impc
Tugon fliegenkugel
Unden (Pesticide)
Bayer B 5122
Bayer 39007
Propoksuru
Chemagro 9010
Unden 50PM
PHC 7
2-(1-Methylethoxy)phenol methylcarbamate
Bay 9010
ENT 25,671
Phenol, 2-(1-methylethoxy)-, methylcarbamate
O-(2-Isopropoxyphenyl) N-methylcarbamate
BAY 5122
o-Isopropoxyphenyl N-methylcarbamate
BAY 39007
Phenol, o-isopropoxy-, methylcarbamate
2-(1-methylethoxy)phenyl methylcarbamate
CHEBI:34938
o-Isopropoxyphenyl methylcarbamate
2-Isopropoxyphenyl-N-methylcarbamat
Carbamic acid, methyl-, o-isopropoxyphenyl ester
NSC-379584
2-Methylethoxyphenyl carbamate
2-(1-Methylethoxy)phenyl N-methylcarbamate
BFH029TL73
(2-propan-2-yloxyphenyl) N-methylcarbamate
DTXSID7021948
2-(propan-2-yloxy)phenyl methylcarbamate
2-[(1-methylethyl)oxy]phenyl methylcarbamate
PHC (carbamate)
DTXCID301948
Propoksuru [Polish]
Caswell No. 508
CAS-114-26-1
NSC 379584
CCRIS 1392
HSDB 603
OMS-33
Propoxur [INN:BAN]
EINECS 204-043-8
EPA Pesticide Chemical Code 047802
BRN 1879891
UNII-BFH029TL73
Pillargon
Propogon
Boygon
AI3-25671
OMS 33
2-Isopropoxyphenyl-N-methylcarbamat [German]
Propoxur (BAN)
MFCD00055455
Propoxur (Standard)
Bolfo (TN)
Spectrum_001923
PROPOXUR [HSDB]
SpecPlus_000554
PROPOXUR [JAN]
PROPOXUR [MI]
Spectrum2_001232
Spectrum3_000857
Spectrum4_000697
Spectrum5_002032
PROPOXUR [MART.]
SCHEMBL27794
BSPBio_002473
KBioGR_001193
KBioSS_002465
SPECTRUM330066
MLS002207242
BIDD:ER0307
DivK1c_006650
SPBio_001104
Isopropoxyphenyl methylcarbamate
CHEMBL446060
HY-B0916R
ISRUGXGCCGIOQO-UHFFFAOYSA-
KBio1_001594
KBio2_002458
KBio2_005026
KBio2_007594
KBio3_001973
HMS3264G19
Pharmakon1600-00330066
HY-B0916
MSK20270
2-Isopropoxyphenyl-N-methylcarbamate
N-Methyl-2-isopropoxyphenylcarbamate
Tox21_201968
Tox21_301207
BDBM50064617
CCG-39115
NSC379584
NSC755890
AKOS015889907
NSC-755890
NCGC00094544-01
NCGC00094544-02
NCGC00094544-03
NCGC00094544-04
NCGC00094544-05
NCGC00094544-06
NCGC00094544-07
NCGC00255104-01
NCGC00259517-01
AS-50078
SMR000778062
2-(1-Methylethoxy)phenyl methyl carbamate
SBI-0052551.P002
DB-041207
NS00010600
P2894
Propoxur, PESTANAL(R), analytical standard
D08442
O10810
AB00053059_04
Q411303
SR-01000872751
SR-01000872751-1
BRD-K08231299-001-08-1
Phenol, 2-(1-methylethoxy)-, 1-(N-methylcarbamate)
Carbamic acid, methyl-, 2-(1-methylethoxy)phenyl ester
InChI=1/C11H15NO3/c1-8(2)14-9-6-4-5-7-10(9)15-11(13)12-3/h4-8H,1-3H3,(H,12,13)
PHC