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Promecarb

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Identification
Molecular formula
C12H17NO2
CAS number
2631-37-0
IUPAC name
(3-isopropyl-5-methyl-phenyl) N-methylcarbamate
State
State

At room temperature, Promecarb is in a solid state, typically appearing as crystalline powder.

Melting point (Celsius)
48.00
Melting point (Kelvin)
321.15
Boiling point (Celsius)
324.00
Boiling point (Kelvin)
597.15
General information
Molecular weight
207.27g/mol
Molar mass
207.2700g/mol
Density
1.0400g/cm3
Appearence

Promecarb appears as a white to off-white crystalline solid. It tends to have a slight odor characteristic of carbamates. The material is often available in technical form or in formulated products with varying degrees of purity.

Comment on solubility

Solubility of (3-isopropyl-5-methyl-phenyl) N-methylcarbamate

(3-isopropyl-5-methyl-phenyl) N-methylcarbamate is a compound with intriguing solubility characteristics. Its solubility in various solvents can provide insights into its behavior in different environments. Here are some key points regarding its solubility:

  • Polar Solvents: This compound is expected to have limited solubility in polar solvents like water due to the presence of bulky isopropyl and methyl groups, which hinder strong solute-solvent interactions.
  • Non-polar Solvents: It is likely to demonstrate better solubility in non-polar or slightly polar organic solvents such as hexane or toluene. The hydrocarbon chains facilitate favorable interactions.
  • Temperature Dependency: The solubility may increase with temperature, a common phenomenon for many organic compounds, due to enhanced molecular movement and interactions.
  • Functional Groups: The presence of the carbamate functional group contributes to its overall solubility characteristics, potentially allowing for limited interaction with polar solvents.

In summary, while (3-isopropyl-5-methyl-phenyl) N-methylcarbamate might exhibit varied solubility depending on the solvent and conditions, understanding these aspects is crucial for applications in chemical synthesis and formulations.

Interesting facts

Interesting Facts about (3-isopropyl-5-methyl-phenyl) N-methylcarbamate

(3-isopropyl-5-methyl-phenyl) N-methylcarbamate is a fascinating compound that belongs to the class of carbamates. Known for their wide array of applications, carbamates are often used in pharmaceuticals, agriculture, and industrial processes. Here are some engaging insights about this particular compound:

  • Mechanism of Action: As a carbamate, this compound functions primarily as a reversible inhibitor of acetylcholinesterase. This means it can influence neurotransmission by inhibiting the breakdown of acetylcholine, leading to increased levels of this important neurotransmitter.
  • Applications: Compounds like (3-isopropyl-5-methyl-phenyl) N-methylcarbamate are frequently explored for their insecticidal properties, making them valuable in agricultural practices. They help in protecting crops from pests, thus promoting food security.
  • Safety and Precautions: As with many chemical compounds, it is crucial to approach (3-isopropyl-5-methyl-phenyl) N-methylcarbamate with caution. Users must adhere to safety guidelines to mitigate any potential health risks associated with exposure, particularly when handling in large quantities.
  • Structural Diversity: The compound exhibits structural characteristics typical of carbamate derivatives, which often contribute to their very diverse biological activity and therapeutic potentials.
  • Research Interest: Ongoing research explores not just the utility of this compound, but also its environmental impact and ways to enhance efficacy while reducing toxicity to non-target organisms.

In summary, (3-isopropyl-5-methyl-phenyl) N-methylcarbamate exemplifies the important role of synthetic compounds in modern science, emphasizing the need for responsible usage and further research into their broader implications. Its dual capabilities in agriculture and neuroscience make it a compound of interest for both chemists and agronomists alike.

Synonyms
PROMECARB
Carbamult
2631-37-0
Minacide
Promecarbe
m-Cym-5-yl methylcarbamate
Schering 34615
Morton EP-316
Nor-Am
Sch 34615
Sn-316
OMS 716
5-Methyl-m-cumenyl methylcarbamate
ENT 27,300-a
Caswell No. 271C
Promecarb [BSI:ISO]
3-Isopropyl-5-methylphenyl methylcarbamate
3-Methyl-5-isopropylphenyl methylcarbamate
EP 316
Carbamic acid, methyl-, m-cym-5-yl ester
3-Isopropyl-5-methylphenyl N-methylcarbamate
Promecarbe [ISO-French]
UC 9880
Union carbide UC-9880
RCRA waste no. P201
SN 34615
NSC 35378
Phenol, 3-methyl-5-(1-methylethyl)-, methylcarbamate
HSDB 1554
5-Isopropyl-m-tolyl methylcarbamate
ENT 27300-A
EINECS 220-113-0
3-Methyl-5-isopropylphenyl N-methylcarbamate
ENT 27300
Methylcarbamic acid m-cym-5-yl ester
EPA Pesticide Chemical Code 271400
UNII-1QRP20775S
3-Methyl-5-isopropyl N-methylcarbamate
BRN 2111695
DTXSID4037617
CHEBI:82096
AI3-27300
1QRP20775S
Phenol, 3-methyl-5-(1-methylethyl)-, methyl carbamate
3-Methyl-5-isopropylphenyl-N-methylcarbamate
PROMECARB [ISO]
PROMECARB [MI]
PROMECARB [HSDB]
Carbamic acid, N-methyl-, 3-methyl-5-isopropylphenyl ester
NSC-35378
3-Methyl-5-(1-methylethyl)phenolmethylcarbamate
3-Methyl-5-(1-methylethyl)phenol methylcarbamate
3-Methyl-5-(1-methylethyl)phenyl methylcarbamate
(3-Methyl-5-isopropylphenyl)-N-methylcarbamat [German]
DTXCID2017617
(3-Methyl-5-isopropylphenyl)-N-methylcarbamat
Carbamic acid, methyl-, 3-methyl-5-(1-methylethyl)phenyl ester
EP-316
SCH-34615
SN-34615
Promecarbe (ISO-French)
3-METHYL-5-(1-METHYLETHYL)PHENYL N-METHYLCARBAMATE
4111-89-1
3-cym-5-yl methylcarbamate
NorAm
Morton EP316
mCym5yl methylcarbamate
Union Carbide UC9880
5Methylmcumenyl methylcarbamate
5Isopropylmtolyl methylcarbamate
Methylcarbamic acid mcym5yl ester
3Methyl5isopropyl Nmethylcarbamate
ENT 27300A
SN316
ENT 27,300A
Carbamic acid, methyl, mcym5yl ester
3Isopropyl5methylphenyl methylcarbamate
3Methyl5isopropylphenyl methylcarbamate
3Methyl5isopropylphenylNmethylcarbamate
(3Methyl5isopropylphenyl)Nmethylcarbamat
3Isopropyl5methylphenyl Nmethylcarbamate
3Methyl5(1methylethyl)phenolmethylcarbamate
3Methyl5(1methylethyl)phenol methylcarbamate
3Methyl5(1methylethyl)phenyl methylcarbamate
5-ISOPROPYL-M-TOLYL METHYL-CARBAMATE
3-Methyl-5-isopropylphenyl N-methylcarbamatecid
Phenol, 3methyl5(1methylethyl), methylcarbamate
3-methyl-5-(propan-2-yl)phenyl N-methylcarbamate
Carbamic acid, Nmethyl, 3methyl5isopropylphenyl ester
Carbamic acid, methyl, 3methyl5(1methylethyl)phenyl ester
CARBANILIC ACID, 3-ISOPROPYL-5-METHYL-, METHYL ESTER
Phenol, 3-methyl-5-(1-methylethyl)-, methylcarbamate (9CI)
PHENOL, 3-METHYL-5-(1-METHYLETHYL)-,METHYLCARBAMATE
CARBAMIC ACID,(3-METHYL-5-(1-METHYLETHYL)PHENYL)-, METHYL ESTER
220-113-0
dtapqajkafrnjb-uhfffaoysa-n
(3-methyl-5-propan-2-ylphenyl) N-methylcarbamate
Phenol, 3-methyl-5-(1-methylethyl)-, 1-(N-methylcarbamate)
T-32
SCHEMBL121314
CHEMBL1076537
Carbamic acid, m-cym-5-yl ester
WLN: 1Y1&R C1 EOVM1
NSC35378
Tox21_301424
Promecarb 100 microg/mL in Cyclohexane
NCGC00163793-01
NCGC00255587-01
LS-14104
CAS-2631-37-0
DB-046925
NS00003842
Promecarb, PESTANAL(R), analytical standard
C18956
Carbamic acid, 3-methyl-5-isopropylphenyl ester
Q7249684
Phenol,3-methyl-5-(1-methylethyl)-,1-(N-methylcarbamate)