Skip to main content

Carbamate

ADVERTISEMENT
Identification
Molecular formula
C9H12N2O2
CAS number
1646-88-4
IUPAC name
(3-aminophenyl) N,N-dimethylcarbamate
State
State

At room temperature, (3-aminophenyl) N,N-dimethylcarbamate is typically in a solid state.

Melting point (Celsius)
62.00
Melting point (Kelvin)
335.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
180.20g/mol
Molar mass
180.2040g/mol
Density
1.0280g/cm3
Appearence

(3-Aminophenyl) N,N-dimethylcarbamate appears as a white to off-white crystalline solid. It may also come in powder form, depending on its preparation and handling.

Comment on solubility

Solubility of (3-aminophenyl) N,N-dimethylcarbamate

The solubility of (3-aminophenyl) N,N-dimethylcarbamate is a critical property that influences its application in various chemical processes. Generally, this compound is categorized as follows:

  • Solvent Interaction: It exhibits moderate solubility in polar solvents such as water and alcohols, which is indicative of the presence of both hydrophilic and hydrophobic regions in its molecular structure.
  • Temperature Dependence: The solubility typically increases with temperature, a common characteristic for many organic compounds, making higher temperatures advantageous for dissolving this substance.
  • pH Sensitivity: The solubility might vary based on pH conditions, as the ionization of the amino group can affect its solubility profile in aqueous solutions.

In summary, understanding the solubility of (3-aminophenyl) N,N-dimethylcarbamate is vital for optimizing its use in formulations and reactions, facilitating enhanced delivery and reactivity in diverse chemical environments.

Interesting facts

Interesting Facts about (3-aminophenyl) N,N-dimethylcarbamate

(3-aminophenyl) N,N-dimethylcarbamate, also known in some contexts as a form of a carbamate compound, is noteworthy for several intriguing aspects:

  • Biological Relevance: This compound has gained attention in pharmacology and biochemistry due to its potential as a pharmaceutical intermediate. Its structure allows for the modification that can lead to various bioactive agents.
  • Mechanistic Insights: Compounds like (3-aminophenyl) N,N-dimethylcarbamate are often studied for their inhibitory effects on key enzymes. This can grant insights into their mechanisms of action, which is essential for drug development.
  • Environmental Impact: The carbamate class of compounds is significant in environmental chemistry, where their degradation pathways are crucial for understanding toxicity and biodegradability. This makes them relevant in studies of pollution and environmental safety.
  • Structure-Activity Relationships: Chemists are fascinated by how slight variations in the carbon chain or amino groups can lead to drastic changes in the pharmacological activity of these compounds. This relation is essential for rational drug design.

In summary, the study of (3-aminophenyl) N,N-dimethylcarbamate encompasses various scientific disciplines, offering a rich field for exploration in both medicinal chemistry and environmental science. Its dual roles underline the importance of such compounds in both therapeutic applications and ecological considerations.

Synonyms
3-AMINOPHENYL DIMETHYLCARBAMATE
19962-04-0
DTXSID50173753
DTXCID3096244
RefChem:276669
(3-aminophenyl) N,N-dimethylcarbamate
3-aminophenyl N,N-dimethylcarbamate
MFCD00052699
Carbamic acid, N,N-dimethyl-, 3-aminophenyl ester
3-AMINOPHENYL N,N-DIMETHYLCARBAMATE, 97
VTC
Neostigmine Impurity 4
Maybridge4_003931
SCHEMBL1446527
SCHEMBL31522632
LKEQZFMJKLCAEA-UHFFFAOYSA-N
HMS1532C15
3-AMINOPHENYLDIMETHYLCARBAMATE
CCG-48397
AKOS006275119
IDI1_032753
DS-12637
SY119598
CS-0151342
C73781
SR-01000637943-1
BRD-K33512039-001-01-3