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(4-benzylphenyl) carbamate

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Identification
Molecular formula
C14H13NO2
CAS number
.
IUPAC name
(4-benzylphenyl) carbamate
State
State
At room temperature, (4-benzylphenyl) carbamate remains in a solid state. The compound is typically stable under normal environmental conditions.
Melting point (Celsius)
94.00
Melting point (Kelvin)
367.00
Boiling point (Celsius)
407.00
Boiling point (Kelvin)
680.00
General information
Molecular weight
227.27g/mol
Molar mass
227.2670g/mol
Density
1.0800g/cm3
Appearence

(4-benzylphenyl) carbamate is an organic compound which may appear as a white or off-white crystalline solid. The compound has a crystalline structure that exhibits sheen under light, typical for aromatic structures with complex substituents.

Comment on solubility

Solubility of (4-benzylphenyl) carbamate

(4-benzylphenyl) carbamate is a compound that exhibits unique solubility characteristics. Generally, the solubility of organic compounds, such as this one, is influenced by various factors including polarity, temperature, and the presence of different solvents.

When discussing the solubility of (4-benzylphenyl) carbamate, consider the following key points:

  • Polarity: Due to its carbamate group, this compound has a certain degree of polarity, which can enhance its solubility in polar solvents like water.
  • Solvents: It is typically more soluble in organic solvents such as ethanol, methanol, and acetone due to its hydrophobic aromatic structures.
  • Temperature: Like many organic compounds, the solubility may increase with elevated temperatures, making it more effective for applications requiring mixed solvents.
  • Saturation: At certain concentrations, (4-benzylphenyl) carbamate could reach a saturation point in solvents, leading to precipitation. This is an essential consideration in practical applications.

As a compound combining both hydrophilic and hydrophobic parts, the solubility profile of (4-benzylphenyl) carbamate reflects a delicate balance. Therefore, to achieve optimal use and effects, understanding its solubility behavior is crucial.

Interesting facts

Interesting Facts about (4-benzylphenyl) carbamate

(4-benzylphenyl) carbamate, a fascinating organic compound, showcases intriguing properties and applications in various fields of chemistry. Here are some compelling aspects that make it a subject of interest:

  • Structural Significance: This compound features a unique arrangement that includes both a benzyl group and a phenyl group, making its structure ideal for studying intermolecular interactions.
  • Biological Activities: There is growing interest in the potential biological activities of carbamates, particularly in pharmacology and as agrochemicals. Some derivatives exhibit significant antimicrobial and anti-inflammatory properties.
  • Versatile Reactivity: As a carbamate, it can undergo various chemical reactions such as hydrolysis and transesterification, making it a versatile building block in organic synthesis.
  • Synthetic Applications: (4-benzylphenyl) carbamate serves as a precursor for the synthesis of more complex molecules, often used in the development of pharmaceuticals and other specialty chemicals.
  • Research Studies: Ongoing research into carbamates emphasizes their role in drug design, sustainability, and agrochemical formulations, positioning them as crucial components in modern chemistry.

The intriguing structure and potential applications of (4-benzylphenyl) carbamate not only contribute to its scientific interest but also inspire future innovations in chemistry and related fields. As emphasized by many researchers, "Understanding such compounds could pave the way for groundbreaking advancements!"

Synonyms
Diphenan
Diphenane
Carbaurine
Carphenol
Parabencil
101-71-3
Oxybulan
Palafuge
Butolan
Butolen
p-Benzylphenyl carbamate
(4-benzylphenyl) carbamate
difenan
Parabencilfenol
Difenano
Diphenanum
Diphenan [INN:DCF]
Difenano [INN-Spanish]
Diphenane [INN-French]
Diphenanum [INN-Latin]
Diphenan (pharmaceutical)
Parabencilfenol [Spanish]
.alpha.-Phenyl-p-cresol carbamate
GNF-Pf-1544
4-Benzylphenyl carbamate
4-(Phenylmethyl)phenol carbamate
p-Cresol, alpha-phenyl-, carbamate
U129BBY8DB
NSC-60023
Phenol, 4-(phenylmethyl)-, carbamate
BRN 3295222
alpha-Phenyl-p-cresol carbamate
DTXSID4046234
Diphenan, pharmaceutical
DIPHENAN [INN]
DIPHENANE [MI]
DTXCID2026234
3-06-00-03360 (Beilstein Handbook Reference)
NSC 60023
NCGC00160564-01
Difenano (INN-Spanish)
Diphenane (INN-French)
Diphenanum (INN-Latin)
p-Hydroxydiphenylmethane carbamic acid ester
Carbamic acid, .alpha.-phenyl-p-tolyl ester
UNII-U129BBY8DB
Phenol, carbamate
p-Cresol, carbamate
SCHEMBL667724
CHEMBL608856
CHEBI:134933
ZBJBRUSGEJORQL-UHFFFAOYSA-N
[4-(Phenylmethyl)phenyl] carbamate
AAA10171
NSC60023
Tox21_111903
AKOS024332138
p-Cresol, .alpha.-phenyl-, carbamate
CAS-101-71-3
DB-249442
NS00114020
SR-01000945032
SR-01000945032-1
Q27290543
622-919-1