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Carbendazim

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Identification
Molecular formula
C9H9ClBrN2O2
CAS number
10605-21-7
IUPAC name
3-(4-bromo-3-chloro-phenyl)-1-methoxy-1-methyl-urea
State
State

At room temperature, carbendazim is in a solid state, specifically a powdery solid.

Melting point (Celsius)
302.00
Melting point (Kelvin)
575.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
191.97g/mol
Molar mass
191.9710g/mol
Density
1.9300g/cm3
Appearence

Carbendazim typically presents as an off-white or light gray solid. It is commonly found as a crystalline powder and may seem slightly yellowish depending on the purity and specific formulation used in different chemical preparations.

Comment on solubility

Solubility of 3-(4-bromo-3-chloro-phenyl)-1-methoxy-1-methyl-urea

The solubility characteristics of 3-(4-bromo-3-chloro-phenyl)-1-methoxy-1-methyl-urea (C9H9ClBrN2O2) reveal important insights into its chemical behavior in various solvents. When assessing solubility, several factors come into play, including molecular structure, polarity, and interactions with the solvent.

  • Polarity: The presence of polar functional groups, such as the urea unit and the methoxy group, suggests that this compound may exhibit moderate solubility in polar solvents like water or methanol.
  • Halogen Substituents: The introduction of chlorine and bromine atoms can affect the overall hydrophobic nature of the compound, potentially leading to decreased solubility in highly polar solvents.
  • Solvent Interactions: When considering solubility, it is crucial to remember that "like dissolves like." Therefore, this compound may show better solubility in organic solvents such as ethyl acetate or dimethyl sulfoxide (DMSO).

In summary, while 3-(4-bromo-3-chloro-phenyl)-1-methoxy-1-methyl-urea may have some solubility in polar solvents due to its functional groups, it may also exhibit significant solubility in nonpolar or slightly polar organic solvents due to its halogen content. Experimental solubility tests would provide definitive insights into its behavior across a range of solvent systems.

Interesting facts

Interesting Facts about 3-(4-bromo-3-chloro-phenyl)-1-methoxy-1-methyl-urea

This compound, known as 3-(4-bromo-3-chloro-phenyl)-1-methoxy-1-methyl-urea, is a fascinating example of how the modification of simple molecular structures can lead to a wide variety of applications in the field of chemistry. Here are some intriguing aspects:

  • Pharmaceutical Importance: This compound showcases the potential for urea derivatives in medicinal chemistry. Many urea derivatives are known for their effectiveness as drugs, particularly in the areas of anti-inflammatory and anti-cancer therapies.
  • Structural Diversity: The presence of bromine and chlorine atoms in the compound contributes to its unique properties. Halogenated compounds often display enhanced biological activity. This structural diversity can lead to different metabolic pathways in organisms.
  • Organic Synthesis: The versatility of substituents in this compound makes it a valuable building block in organic synthesis. Chemists can utilize such compounds to explore various routes for synthesizing complex molecules.
  • Environmental Impact: Studies have shown that brominated compounds, like this one, can accumulate in ecosystems. Understanding their stability and degradation pathways is crucial for assessing environmental risks.
  • Mechanistic Insights: The role of methoxy groups in modifying chemical reactivity provides valuable insight into the mechanisms of action in biological systems. This aspect is essential for designing new drugs with enhanced efficacy.

With its combination of halogen substituents and urea functional group, this compound serves as a critical point of study for chemists interested in both basic and applied research. As stated by a noted chemist, "The elegance of complexity in molecular design often lies in the details of substitution."

Exploring the properties and behaviors of compounds like 3-(4-bromo-3-chloro-phenyl)-1-methoxy-1-methyl-urea not only broadens our understanding of organic molecules but also paves the way for innovative advancements in pharmaceuticals and materials science.

Synonyms
CHLORBROMURON
13360-45-7
Chlorobromuron
Maloran
Bromex (herbicide)
3-(4-Bromo-3-chlorophenyl)-1-methoxy-1-methylurea
Caswell No. 173A
Ciba 6313
Chlorbromuron [BSI:ISO]
Chlorobromuron [ISO-French]
HSDB 1536
UNII-2X2DQC5EHG
2X2DQC5EHG
EINECS 236-411-9
Urea, N'-(4-bromo-3-chlorophenyl)-N-methoxy-N-methyl-
C 6313
EPA Pesticide Chemical Code 090701
BRN 2128736
DTXSID6040290
1-(3-Chloro-4-bromophenyl)-3-methyl-3-methoxyurea
N'-(4-Bromo-3-chlorophenyl)-N-methoxy-N-methylurea
N-(4-Bromo-3-chlorophenyl)-N'-methoxy-N'-methylurea
Urea, 3-(4-bromo-3-chlorophenyl)-1-methoxy-1-methyl-
C-6313
CHLORBROMURON [ISO]
1-(4-bromo-3-chlorophenyl)-3-methoxy-3-methylurea
CHLORBROMURON [HSDB]
DTXCID4020290
Chlorobromuron (ISO-French)
3-(4-bromo-3-chloro-phenyl)-1-methoxy-1-methyl-urea
N'-(4-Bromo-3-chlorophenyl)-N-methhoxy-N-methylurea (8CI)
N'-(4-Bromo-3-chlorophenyl)-N-methhoxy-N-methylurea (8CI)(9CI)
1(3Chloro4bromophenyl)3methyl3methoxyurea
3(4Bromo3chlorophenyl)1methoxy1methylurea
N(4Bromo3chlorophenyl)N'methoxyN'methylurea
C6313
Urea, 3(4bromo3chlorophenyl)1methoxy1methyl
Urea, N'(4bromo3chlorophenyl)NmethoxyNmethyl
N'(4Bromo3chlorophenyl)NmethhoxyNmethylurea (8CI)
N'(4Bromo3chlorophenyl)NmethhoxyNmethylurea (8CI)(9CI)
236-411-9
bromex
nlynutmztclnoo-uhfffaoysa-n
Chlorobromouron
CHEBI:3608
Chlorbromuron 100 microg/mL in Acetonitrile
SCHEMBL65119
CHEMBL1275654
Tox21_300793
NCGC00166178-01
NCGC00166178-02
NCGC00254697-01
CAS-13360-45-7
NS00008128
Chlorobromouron, PESTANAL(R), analytical standard
N'-(4-Bromo-3-chlorophenyl)-N-methhoxy-N-methylurea
Q22807251
N'-(4-Bromo-3-chlorophenyl)-N-methoxy-N-methylurea #