Interesting facts
Interesting Facts about (2-isopropylphenyl) N-methylcarbamate
(2-isopropylphenyl) N-methylcarbamate is a fascinating compound with applications that reflect its unique chemical structure and properties. Here are some noteworthy facts:
- Applications in Agriculture: This compound is often used as a pesticide. It showcases the vital role of carbamate derivatives in protecting crops from pests while being less toxic to humans and wildlife compared to other pesticide classes.
- Mechanism of Action: As a carbamate, it works by inhibiting the enzyme acetylcholinesterase, which plays a crucial role in neurotransmission. By blocking this enzyme, it disrupts the normal function of neurotransmitters, leading to pest mortality.
- Structurally Unique: The presence of the 2-isopropylphenyl group contributes to the compound's lipophilicity, allowing it to penetrate biological membranes effectively. This structural characteristic impacts its overall efficacy and pharmacokinetics.
- Sustainability Considerations: As the agricultural sector moves toward more sustainable practices, compounds like (2-isopropylphenyl) N-methylcarbamate are being scrutinized for environmental impact. Research continues to optimize its use while minimizing ecological risks.
- Regulatory Status: Like many pesticides, (2-isopropylphenyl) N-methylcarbamate is subjected to rigorous evaluation by regulatory agencies. This ensures it meets safety standards and efficacy before being approved for various agricultural applications.
In summary, (2-isopropylphenyl) N-methylcarbamate stands as an example of the intricate relationship between chemical structure and biological function, highlighting the ongoing evolution of chemistry in addressing modern agricultural challenges.
Synonyms
Isoprocarb
2631-40-5
Etrofolan
2-Isopropylphenyl methylcarbamate
Mipcine
Mipcin
o-Cumenyl methylcarbamate
Hytox
2-Isopropylphenyl N-methylcarbamate
o-Cumenyl N-methylcarbamate
Mipsin
o-Isopropylphenol methylcarbamate
Isoprocarbe
o-Isopropylphenyl methylcarbamate
o-Isopropylphenyl N-methylcarbamate
PPC 3
Isopropylphenol methylcarbamate
Phenol, 2-(1-methylethyl)-, 1-(N-methylcarbamate)
Carbamic acid, methyl-, o-cumenyl ester
Phenol, 2-(1-methylethyl)-, methylcarbamate
Ro 7-5050
Bayer 39731
BAY 39731
ENT 25670
Caswell No. 512B
KHE 0145
Isoprocarb [BSI:ISO]
BAY 105807
NSC 191479
Isoprocarbe [ISO-French]
2-(1-Methylethyl)phenol methylcarbamate
2-(1-Methylethyl)phenyl methylcarbamate
Phenol, O-isopropyl-, methylcarbamate
Etrolan
OMS-32
Carbamic acid, methyl-, o-isopropylphenyl ester
EINECS 220-114-6
Carbamic acid, methyl-, 2-(1-methylethyl)phenyl ester
EPA Pesticide Chemical Code 512300
BRN 1875020
Isopropyl phenylmethyl carbamate
DTXSID6042072
CHEBI:38505
N-Methyl-2-isopropylphenylcarbam
AI3-25670
714I55QH9K
Isoprocarb, BSI, ISO
MIPC, JMAF
Cumenyl N-methylcarbamate
ISOPROCARB [ISO]
Methylcarbamic acid, o-cumenyl ester
2-(propan-2-yl)phenyl methylcarbamate
NSC-191479
2-(propan-2-yl)phenyl N-methylcarbamate
DTXCID4022072
4-06-00-03212 (Beilstein Handbook Reference)
BAY-39731
ENT-25670
2-(1-Methylethyl)phenyl methylcarbamate, 9CI
Isoprocarbe (ISO-French)
2-(1-METHYLETHYL)PHENYL N-METHYLCARBAMATE
phenyl-2-(1-methylethyl)methylcarbamate
2-Isopropylphenyl methylcarbamic acid
N-methyl-1-2-(propan-2-yl)phenoxymethanimidic acid
220-114-6
(2-propan-2-ylphenyl) N-methylcarbamate
OMS 32
Bayer 39,731
UNII-714I55QH9K
Isoprocarb solution
WLN: 1YR BOVM1
SCHEMBL64155
Carbamic acid, o-cumenyl ester
CHEMBL2251586
QBSJMKIUCUGGNG-UHFFFAOYSA-
N-Methyl-2-isopropylphenylcarbamate
CAA63140
HY-B0830
MSK20253
Tox21_301361
NSC191479
AKOS006229087
Carbamic acid, o-isopropylphenyl ester
NCGC00160600-01
NCGC00255918-01
AS-80767
2-(1-Methylethyl)-phenol methyl-carbamate
CAS-2631-40-5
DB-046926
CS-0012844
NS00010531
Isoprocarb, PESTANAL(R), analytical standard
C18418
Q27117880
InChI=1/C11H15NO2/c1-8(2)9-6-4-5-7-10(9)14-11(13)12-3/h4-8H,1-3H3,(H,12,13)
Solubility of (2-isopropylphenyl) N-methylcarbamate
The solubility of (2-isopropylphenyl) N-methylcarbamate can be influenced by various factors such as temperature, pH, and the solvent used. Here are some key points to consider:
Understanding the solubility characteristics of (2-isopropylphenyl) N-methylcarbamate is essential for its applications in various chemical processes and formulations. As an intriguing point, compounds with similar structures often exhibit vastly different solubility profiles, illustrating the complexity of chemical interactions in solutions.