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Carbendazim

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Identification
Molecular formula
C9H9N3O2
CAS number
10605-21-7
IUPAC name
ethyl N-(1H-benzimidazol-2-yl)carbamate
State
State

Carbendazim is in a solid state at room temperature. It is commonly used in powder form as a fungicide.

Melting point (Celsius)
302.00
Melting point (Kelvin)
575.15
Boiling point (Celsius)
450.00
Boiling point (Kelvin)
723.15
General information
Molecular weight
192.19g/mol
Molar mass
192.1930g/mol
Density
1.4500g/cm3
Appearence

Carbendazim appears as a white to light brown powder. It is typically odorless and has a crystalline texture.

Comment on solubility

Solubility of Ethyl N-(1H-benzimidazol-2-yl)carbamate

Ethyl N-(1H-benzimidazol-2-yl)carbamate is an intriguing compound with notable solubility characteristics. Understanding its solubility is essential for its application in various fields. Here are some insights regarding its solubility:

  • Solvent Dependence: The solubility of this compound can be highly dependent on the solvent used. Common solvents include organic solvents such as ethanol and methanol.
  • Temperature Effects: Typically, an increase in temperature results in enhanced solubility for many organic compounds. Testing at different temperatures may reveal significant variations in solubility.
  • pH Sensitivity: The solubility can also be affected by the pH of the solution. Adjusting the pH may optimize the dissolution of the compound.
  • Precaution: When working with this compound, it is advisable to perform solubility tests in small scale to determine the best solvent and conditions for dissolution.

In summary, while the solubility of ethyl N-(1H-benzimidazol-2-yl)carbamate in various solvents is an essential consideration, factors such as temperature and pH can significantly influence the overall dissolution process. Experimentation and careful analysis will provide the best insights into its solubility behaviors.

Interesting facts

Interesting Facts about Ethyl N-(1H-benzimidazol-2-yl)carbamate

Ethyl N-(1H-benzimidazol-2-yl)carbamate is a fascinating compound with a variety of interesting applications and features. Here are some noteworthy points:

  • Pharmacological Significance: This compound is known for its potential use in medicinal chemistry. It has shown promise as an active ingredient in various pharmacological studies, particularly due to its benzimidazole moiety.
  • Mechanism of Action: The benzimidazole structure is notable for its ability to interact effectively with biological targets, especially in the inhibition of certain enzymes, making it a focus in drug discovery.
  • Applications in Agriculture: Compounds similar to ethyl N-(1H-benzimidazol-2-yl)carbamate have been explored for their fungicidal properties, showcasing their potential utility in agricultural settings for protecting crops.
  • Research Potential: Current research continues to investigate this compound's efficacy against various pathogens, positioning it as a candidate for further exploration in both therapeutic and agricultural markets.
  • Structural Highlight: The compound features a carbamate functional group, which is key in enhancing biological activity while providing solubility in various solvents, pivotal for formulation development.

This compound epitomizes the intersection of organic chemistry and practical applications, as scientists continue to unlock its potential. With ongoing research, one can only anticipate the groundbreaking discoveries that could stem from the study of ethyl N-(1H-benzimidazol-2-yl)carbamate and similar compounds.

Synonyms
Lobendazole
6306-71-4
Ethyl 2-benzimidazolecarbamate
ethyl (1H-benzo[d]imidazol-2-yl)carbamate
Lobendazol
NSC-42044
SK&F 24529
ethyl N-(1H-benzimidazol-2-yl)carbamate
Ethyl 1H-benzimidazol-2-ylcarbamate
2-Carboethoxyaminobenzimidazole
Ethyl 2-benzimidazolylcarbamate
N-(2'-Benzimidazolyl)-urethane
ethyl 1H-benzo[d]imidazol-2-ylcarbamate
2-Benzimidazolecarbamic acid, ethyl ester
Ethyl N-(2-benzimidazolyl)carbamate
SKF 24529
Benzimidazol-2-ylcarbamate ethyl ester
ethyl N-(1H-1,3-benzodiazol-2-yl)carbamate
N-(2-Benzimidazolyl)carbamic acid ethyl ester
CMF6Z78SWL
2-((Ethoxycarbonyl)amino)benzimidazole
Carbamic acid, 1H-benzimidazol-2-yl-, ethyl ester
Ethyl(1H-benzo[d]imidazol-2-yl)carbamate
N-(1H-BENZIMIDAZOL-2-YL)CARBAMIC ACID ETHYL ESTER
NSC42044
Lobendazolum
Lobendazole [USAN:INN]
Lobendazol [INN-Spanish]
Lobendazolum [INN-Latin]
Ethyl benzimidazolecarbamate
2-[(Ethoxycarbonyl)amino]benzimidazole
Ethyl 1H-benzimidazolylcarbamate
UNII-CMF6Z78SWL
NSC 42044
Benzimidazole carbamate d'ethyle [French]
Benzimidazole carbamate d'ethyle
G 756
delta2,N-Benzimidazolinecarbamic acid, ethyl ester
CARBAMIC ACID, (2-BENZIMIDAZOLYL)-, ETHYL ESTER
CBDZ-M
Lobendazole, ethyl ester
ChemDivAM_000121
LOBENDAZOLE [INN]
Lobendazole (USAN/INN)
.DELTA.2, ethyl ester
ChemDiv1_000153
LOBENDAZOLE [USAN]
MLS006011651
SCHEMBL205437
CHEMBL2105088
CHEBI:92287
HMS587G21
DTXSID70212390
HMS2093J17
Pharmakon1600-01505440
HY-B1313
SKF24529
NSC759134
NSC764935
AKOS000538793
CCG-103228
NSC-759134
NSC-764935
SK&F-24529
NCGC00263896-03
SMR000069102
SBI-0206847.P001
CS-0013074
NS00014513
D04754
EN300-265749
G69396
AB00275634_02
Carbamic acid, 1H-benzimidazol-2-yl-,ethyl ester
SR-05000002015
SR-05000002015-1
BRD-K15834839-001-01-5
BRD-K15834839-001-02-3
Q27164045
F0348-2711