Skip to main content

Bromacil

ADVERTISEMENT
Identification
Molecular formula
C9H13BrN2O2
CAS number
314-40-9
IUPAC name
3-(4-bromophenyl)-1-methoxy-1-methyl-urea
State
State

At room temperature, Bromacil is typically in a solid state in the form of a crystalline powder and does not have a noticeable odor.

Melting point (Celsius)
159.50
Melting point (Kelvin)
432.65
Boiling point (Celsius)
392.70
Boiling point (Kelvin)
665.85
General information
Molecular weight
261.12g/mol
Molar mass
261.0640g/mol
Density
1.6880g/cm3
Appearence

Bromacil is presented in the form of a crystalline solid. It is typically white or off-white in color and is often found as powder or granular form depending on its intended use, especially in herbicidal applications.

Comment on solubility

Solubility of 3-(4-bromophenyl)-1-methoxy-1-methyl-urea

The solubility of 3-(4-bromophenyl)-1-methoxy-1-methyl-urea can be influenced by several factors, including its molecular structure and the presence of functional groups. Here are some key points to consider:

  • Polar and Non-Polar Interactions: This compound features both polar (urea and methoxy groups) and non-polar (bromophenyl ring) characteristics, which can impact its solubility in various solvents.
  • Solvent Compatibility: It is likely to exhibit higher solubility in polar solvents such as water and ethanol due to the presence of the urea moiety and the methoxy group, which can facilitate hydrogen bonding.
  • Temperature Effects: Solubility may increase with temperature; thus, it’s advisable to check solubility at varying temperatures for precise applications.
  • pH Dependence: The solubility of urea derivatives can also be affected by pH levels. Acidic or basic conditions may alter the protonation state and thus influence solubility.

It is essential to conduct empirical solubility tests under controlled conditions to obtain definitive data on the solubility characteristics of this compound. Insert specific solubility values and solvent systems whenever possible, as they provide crucial insights into its behavior in practical applications.

Interesting facts

Interesting Facts about 3-(4-Bromophenyl)-1-methoxy-1-methyl-urea

3-(4-Bromophenyl)-1-methoxy-1-methyl-urea is a fascinating compound that offers a variety of insights and opportunities for exploration in the field of chemistry. Here are some engaging aspects:

  • Pharmaceutical Relevance: This compound belongs to the class of ureas, which have significant importance in medicinal chemistry. Its structural modifications can lead to enhanced biological activity, making it a compound of interest for drug development.
  • Bromophenyl Group: The presence of the 4-bromophenyl group can impart unique electronic properties. The bromine atom can influence the reactivity and interactions of the molecule, making it an intriguing subject for further study.
  • Mechanism of Action: As a urea derivative, this compound may interact with biological targets by mimicking natural substrates, thus providing insight into enzymatic processes and potentially aiding in the design of inhibitors or activators.
  • Synthetic Pathways: The synthesis of this compound often involves creative synthetic strategies that showcase the versatility of organic synthesis techniques. It can serve as a model for aspiring chemists to learn various reactions and mechanisms.
  • Interdisciplinary Applications: Beyond medicinal chemistry, compounds like 3-(4-bromophenyl)-1-methoxy-1-methyl-urea can find applications in agricultural chemistry, offering potential for the development of herbicides or pesticides.

In summary, 3-(4-Bromophenyl)-1-methoxy-1-methyl-urea serves as a prime example of how a simple chemical structure can have far-reaching implications in various scientific fields. Its unique properties make it a worthy compound for investigation, highlighting the intricate connections between structure, function, and application in chemistry.

Synonyms
METOBROMURON
3060-89-7
Patoran
Metobromurone
Urea, N'-(4-bromophenyl)-N-methoxy-N-methyl-
Caswell No. 579A
Metobromuron [ISO]
CCRIS 6765
Metobromuron [ANSI:BSI:ISO]
HSDB 1741
Patoran FL
EINECS 221-301-5
EPA Pesticide Chemical Code 035901
BRN 2103964
DTXSID6042157
UNII-4251089P3L
C-3126
METOBROMURON [MI]
METOBROMURON [HSDB]
4251089P3L
DTXCID4022157
DNDI1246791
N-(p-Bromophenyl)-N'-methyl-N'-methoxyurea
C 3126
Metobromuron (ANSI:BSI:ISO)
CIBA3126
3(pBromophenyl)1methoxy1methylurea
3(pBromophenyl)1methyl1methoxyurea
3(4Bromophenyl)1methoxy1methylurea
N'(4Bromophenyl)NmethoxyNmethylurea
Urea, 3(pbromophenyl)1methoxy1methyl
Urea, N'(4bromophenyl)NmethoxyNmethyl
N(4Bromophenyl)N'methylN'methoxyharnstoff
221-301-5
c3126
wlfdqevoramcim-uhfffaoysa-n
Metbromuron
3-(4-Bromophenyl)-1-methoxy-1-methylurea
Monobromuron
Pattonex
N'-(4-Bromophenyl)-N-methoxy-N-methylurea
CIBA-3126
3-(p-Bromophenyl)-1-methoxy-1-methylurea
3-(4-Bromphenyl)-1-methoxyharnstoff
Urea, 3-(p-bromophenyl)-1-methoxy-1-methyl-
3-(p-Bromophenyl)-1-methyl-1-methoxyurea
1-(4-bromophenyl)-3-methoxy-3-methylurea
CHEBI:81964
Metobromuron 10 microg/mL in Acetonitrile
Metobromuron 100 microg/mL in Acetonitrile
3-(4-Bromphenyl)-1-methoxyharnstoff [German]
N-(4-Bromophenyl)-N'-methyl-N'-methoxy-harnstoff [German]
SCHEMBL53871
N-(4-Bromophenyl)-N'-methyl-N'-methoxy-harnstoff
CHEMBL1356637
Metobromuron, analytical standard
Tox21_301964
AKOS001609255
NCGC00166156-01
NCGC00255893-01
CAS-3060-89-7
DB-047812
HY-154817
CS-0783319
NS00010464
C18793
Metobromuron, PESTANAL(R), analytical standard
Q18213352
Z1269144452