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Fenobucarb

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Identification
Molecular formula
C12H17NO2
CAS number
3766-81-2
IUPAC name
(3-isopropylphenyl) N-methylcarbamate
State
State

At room temperature, Fenobucarb can exist as a solid or liquid, depending on ambient conditions, typically found in a solid crystalline form.

Melting point (Celsius)
28.00
Melting point (Kelvin)
301.00
Boiling point (Celsius)
134.00
Boiling point (Kelvin)
407.00
General information
Molecular weight
193.25g/mol
Molar mass
193.2460g/mol
Density
1.1080g/cm3
Appearence

Fenobucarb appears as a colorless crystalline solid or a colorless to pale yellow liquid, dependent on conditions, with a mild odor.

Comment on solubility

Solubility of (3-isopropylphenyl) N-methylcarbamate

The solubility of (3-isopropylphenyl) N-methylcarbamate, with the chemical formula C12H17NO2, is influenced by several key factors. Here are some insights:

  • Polar and Non-Polar Characteristics: This compound exhibits both polar and non-polar characteristics due to its aliphatic isopropyl group and the presence of the carbamate functional group. This dual nature affects its interactions with solvents.
  • Solvent Interactions: As such, it tends to be more soluble in organic solvents like dimethyl sulfoxide (DMSO) and ethanol, while showing lower solubility in water.
  • Molecular Size: The relatively large molecular size may also contribute to its limited solubility in water, presenting challenges in forming stable aqueous solutions.
  • Temperature Effects: Solubility can increase with temperature, which often allows for greater molecular movement and interaction with solvents.
  • Environmental Considerations: The compound’s solubility in various solvents has implications for its use in agricultural formulations and environmental behavior, particularly how it may distribute in soil and water systems.

In summary, the solubility of (3-isopropylphenyl) N-methylcarbamate is essentially determined by its molecular structure and the interactions it forms with different solvents. Understanding these factors is crucial when considering its applications and environmental impact.

Interesting facts

Interesting Facts About (3-isopropylphenyl) N-methylcarbamate

(3-isopropylphenyl) N-methylcarbamate is a fascinating compound that belongs to the class of carbamates, which are recognized for their diverse applications in both the chemical industry and biological systems. This compound showcases a unique structure characterized by a phenyl group substituted with an isopropyl group and a carbamate functional group.

Key Highlights:

  • Mechanism of Action: Carbamates like (3-isopropylphenyl) N-methylcarbamate often inhibit acetycholinesterase, an important enzyme in the nervous system, leading to prolonged action of acetylcholine, which can be insightful for understanding nerve signal transmission.
  • Applications: Its structural composition suggests potential use in pharmaceuticals as an insecticide or herbicide, contributing significantly to agricultural chemistry and pest management strategies.
  • Synthetic Pathways: This compound can be synthesized via a variety of methods, showcasing the versatility of organic synthesis and providing an exciting opportunity for students to explore chemical reactions involving carbamates.
  • Research Implications: The study of (3-isopropylphenyl) N-methylcarbamate and similar compounds may lead to advancements in developing new insecticides with reduced toxicity to non-target organisms, which is a crucial aspect of environmental chemistry.

As (3-isopropylphenyl) N-methylcarbamate continues to be a subject of interest within both academic and industrial research, scientists are eager to explore its full potential, with significant implications for enhancing crop protection while ensuring ecological sustainability.

In the words of chemists: "The beauty of chemistry lies in its ability to transform simple molecules into complex systems that can solve real-world problems."

Synonyms
m-Cumenyl methylcarbamate
64-00-6
3-Isopropylphenyl methylcarbamate
m-Cumenol methylcarbamate
Hercules 5727
m-Isopropylphenyl methylcarbamate
Compound 10854
m-Isopropylphenyl N-methylcarbamate
Caswell No. 512A
Union carbide 10854
m-Isopropylphenol methylcarbamate
(3-propan-2-ylphenyl) N-methylcarbamate
Methylcarbamic acid m-cumenyl ester
Union carbide uc-10,854
Carbamic acid, methyl-, m-cumenyl ester
HSDB 6376
OMS 162
UC 10854
m-Isopropylphenol N-methylcarbamate
3-Isopropylphenyl N-methylcarbamate
RCRA waste no. P202
N-Methyl m-isopropylphenyl carbamate
N-Methyl-m-isopropylphenyl carbamate
EINECS 200-572-3
N-Methyl 3-isopropylphenyl carbamate
N-Methyl-3-isopropylphenyl carbamate
HER. 5727
Phenol, m-isopropyl-, methylcarbamate
ENT 25,500
EPA Pesticide Chemical Code 047801
UNII-27502G8UZX
AC 5727
3-(1-Methylethyl)phenol methylcarbamate
BRN 2051096
DTXSID1040324
PHENOL, 3-(1-METHYLETHYL)-, METHYLCARBAMATE
Hercules AC-5727
Carbamic acid, methyl-, 3-(1-methylethyl)phenyl ester
H 5727
H 8757
Carbamic acid, N-methyl-, 3-isopropylphenyl ester
m-Kumenylester kyseliny methylkarbaminove
DTXCID9020324
Phenol, 3-(1-methylethyl)-, methyl carbamate
27502G8UZX
CUMENYL METHYLCARBAMATE, M-
Phenol, 3-(1-methylethyl)-, 1-(N-methylcarbamate)
1PC
MIP
Hercules AC 5727
PHENOL, 3-(1-METHYLETHYL)-, METHYLCARBAMATE [HSDB]
Oms-631
OMS-15
3-Isopropylphenyl-N-methylcarbamate
N-Methyl carbamate, m-1-propylphenyl
3-(1-Methylethyl)phenyl methylcarbamate
AI3-25500
m-Kumenylester kyseliny methylkarbaminove [Czech]
Compound 10854(Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 938)
Compound 10854[Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 938]
H-8,757
Hercules AC 5727(Crop Protection Handbook 2004. (Formerly Farm and Chemicals Handbook) Willoughby, OH: Meister Publishing Co., 2004., p. C-146)
Hercules AC 5727[Crop Protection Handbook 2004. (Formerly Farm and Chemicals Handbook) Willoughby, OH: Meister Publishing Co., 2004., p. C-146]
m-Isopropylphenyl-N-methyl carbamate(Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 938)
m-Isopropylphenyl-N-methyl carbamate[Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 938]
N-methyl-3-isopropylphenyl carbamate(Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 938)
N-methyl-3-isopropylphenyl carbamate[Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 938]
N-methyl-m-isopropylphenyl carbamate(Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 938)
N-methyl-m-isopropylphenyl carbamate[Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 938]
UC 10854(Crop Protection Handbook 2004. (Formerly Farm and Chemicals Handbook) Willoughby, OH: Meister Publishing Co., 2004., p. C-146)
UC 10854[Crop Protection Handbook 2004. (Formerly Farm and Chemicals Handbook) Willoughby, OH: Meister Publishing Co., 2004., p. C-146]
Caswell No 512A
ENT 25,543
Hercules-5,727
mCumenol methylcarbamate
mCumenyl methylcarbamate
3-(propan-2-yl)phenyl N-methylcarbamate
OMS15
Union Carbide UC10,854
m-Cumenyl methylcarbamic acid
3IsopropylphenylNmethylcarbamate
mIsopropylphenyl methylcarbamate
3Isopropylphenyl methylcarbamate
OMS 15
OMS631
SCHEMBL5933261
mIsopropylphenol Nmethylcarbamate
mIsopropylphenyl Nmethylcarbamate
NMethylmisopropylphenyl carbamate
CHEMBL2046819
NMethyl3isopropylphenyl carbamate
NMethyl carbamate, m2propylphenyl
NMethyl misopropylphenyl carbamate
OMS-162
Methylcarbamic acid mcumenyl ester
NMethyl 3isopropylphenyl carbamate
Phenol, misopropyl, methylcarbamate
Tox21_302006
ENT 25500
3(1Methylethyl)phenol methylcarbamate
3(1Methylethyl)phenyl methylcarbamate
Carbamic acid, methyl, mcumenyl ester
mKumenylester kyseliny methylkarbaminove
CAS-64-00-6
USEPA/OPP Pesticide Code: 047801
NCGC00255448-01
Phenol, 3(1methylethyl), methyl carbamate
NS00035617
Carbamic acid, Nmethyl, 3isopropylphenyl ester
H8,757
PHENOL,3(1-METHYLETHYL)-,METHYLCARBAMATE
Carbamic acid, methyl, 3(1methylethyl)phenyl ester
Q6712041