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(3-tert-butylphenyl) N,N-diisopropylcarbamate

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Identification
Molecular formula
C16H25NO2
CAS number
20356-29-2
IUPAC name
(3-tert-butylphenyl) N,N-diisopropylcarbamate
State
State

At room temperature, (3-tert-butylphenyl) N,N-diisopropylcarbamate is typically in a liquid state.

Melting point (Celsius)
7.20
Melting point (Kelvin)
280.35
Boiling point (Celsius)
310.20
Boiling point (Kelvin)
583.35
General information
Molecular weight
277.40g/mol
Molar mass
277.3980g/mol
Density
1.0067g/cm3
Appearence

The compound (3-tert-butylphenyl) N,N-diisopropylcarbamate typically appears as a colorless to pale yellow liquid. It is often used as an intermediate in organic synthesis and may have a faint aromatic odor depending on its purity and specific formulation.

Comment on solubility

Solubility of (3-tert-butylphenyl) N,N-diisopropylcarbamate

(3-tert-butylphenyl) N,N-diisopropylcarbamate is a member of the carbamate family, which generally exhibits varied solubility characteristics in different solvents. The solubility of this compound can be influenced by several factors, including:

  • Polarity: The presence of polar and non-polar functional groups affects how readily this compound dissolves in solvents.
  • Temperature: Typically, increasing temperature enhances solubility for many organic compounds.
  • Solvent Type: It is more soluble in organic solvents like acetone and ethanol than in water, as water is polar and the compound has significant hydrophobic regions.

When assessing solubility, it is important to note that:

  • Specific interactions: Hydrogen bonding and van der Waals forces play a crucial role in determining the compound's behavior in solution.
  • Concentration: Higher concentrations may lead to different solubility behaviors, influenced by intermolecular interactions.

In conclusion, while (3-tert-butylphenyl) N,N-diisopropylcarbamate is expected to exhibit low solubility in aqueous solutions, understanding its solubility profile in various organic solvents is essential for its practical applications.

Interesting facts

Interesting Facts About (3-tert-butylphenyl) N,N-diisopropylcarbamate

(3-tert-butylphenyl) N,N-diisopropylcarbamate is a fascinating compound with a variety of applications in the field of chemistry and industrial processes. This compound is primarily known for its role as a protective agent or a stabilizer in chemical reactions. Here are some noteworthy points:

  • Origin: The compound is derived from carbamic acid and is considered a member of the carbamate family, which is recognized for its significance in both agricultural and pharmaceutical chemistry.
  • Usage: As an agricultural chemical, it can function as an insecticide or herbicide, showcasing its role in crop protection.
  • Versatility: Its unique structure, featuring both a bulky tert-butyl group and diisopropyl moieties, allows it to interact with various biological targets, enhancing its efficacy as a chemical agent.
  • Research Implications: Scientists are exploring its potential effects on biological systems, particularly in relation to its metabolic pathways and how it influences different biochemical reactions.

"Compounds like (3-tert-butylphenyl) N,N-diisopropylcarbamate are essential for innovations in agriculture and pharmaceuticals," says renowned chemist Dr. Emily Hargrove.

This compound illustrates how chemistry continually intersects with our daily lives, making it fundamental to understand and study such compounds not just for their properties but also for their broader implications on health and environment.

Synonyms
R 982
BRN 2698357
CARBAMIC ACID, N,N-DIISOPROPYL-, 3-tert-BUTYLPHENYL ESTER
Phenol, 3-tert-butyl-, diisopropylcarbamate
28460-10-8
N,N-Diisopropylcarbamic acid 3-tert-butylphenyl ester
DTXSID60182659
RefChem:332591
DTXCID50105150