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(3-Phenoxyphenyl)methanol

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Identification
Molecular formula
C13H12O2
CAS number
13826-35-2
IUPAC name
(3-phenoxyphenyl)methanol
State
State

At room temperature, (3-Phenoxyphenyl)methanol is typically in a solid state, owing to its crystalline structure and relatively high molecular weight.

Melting point (Celsius)
28.50
Melting point (Kelvin)
301.65
Boiling point (Celsius)
330.50
Boiling point (Kelvin)
603.65
General information
Molecular weight
200.23g/mol
Molar mass
200.2340g/mol
Density
1.1780g/cm3
Appearence

(3-Phenoxyphenyl)methanol is generally observed as a white to pale yellow crystalline solid. Its crystalline nature gives it a distinct, structured appearance.

Comment on solubility

Solubility of (3-phenoxyphenyl)methanol

(3-phenoxyphenyl)methanol, with the chemical formula C13H12O, exhibits notable solubility characteristics that are influenced by its molecular structure and polarity. Understanding its solubility can facilitate its application in various industrial and laboratory settings.

Factors Affecting Solubility

The solubility of (3-phenoxyphenyl)methanol can be analyzed through several key factors:

  • Polarity: The presence of the hydroxyl group (–OH) contributes to polar interactions, enhancing solubility in polar solvents like water.
  • Hydrophobic interactions: The phenoxy groups are hydrophobic, which may limit solubility in water but enhance solubility in organic solvents.
  • Temperature: Increasing temperature generally increases the solubility of organic compounds, including (3-phenoxyphenyl)methanol.

Solubility Behavior

Generally, one might consider the following patterns:

  1. Water Solubility: Limited solubility due to the competing hydrophobic regions.
  2. Organic Solvents: More soluble in organic solvents like ethanol and acetone.
    1. In conclusion, while (3-phenoxyphenyl)methanol shows limited solubility in water, it demonstrates favorable solubility behavior in organic solvents. This balance between its polar and non-polar characteristics makes it an interesting compound for various applications where solvent choice is critical.

Interesting facts

Interesting Facts about (3-phenoxyphenyl)methanol

(3-phenoxyphenyl)methanol, often referred to in the context of medicinal chemistry and organic synthesis, is a fascinating compound with various applications. Here are some noteworthy points about this compound:

  • Structural Features: This compound features a methanol group attached to a phenoxy-substituted phenyl ring system, which can influence its reactivity and solubility properties.
  • Applications in Pharmaceuticals: Compounds like (3-phenoxyphenyl)methanol may have implications in drug development, often serving as intermediates in synthesizing bioactive molecules.
  • Organic Synthesis: The presence of the methanol group can enhance its utility in various organic reactions, such as ether formation and reduction reactions.
  • Research Interests: This compound can be a subject of interest for researchers studying the interaction of phenolic compounds with biological systems, potentially leading to therapeutic applications.
  • Phenoxy Compounds: The phenoxy group (C6H5O) itself is a well-known moiety in medicinal chemistry, often associated with anti-inflammatory and antioxidant activities.

In summary, (3-phenoxyphenyl)methanol serves as more than just a chemical formula; it represents a bridge between organic chemistry and potential therapeutic advancements. Its unique structural characteristics and possible applications in medicinal chemistry highlight the intricate relationship between molecular structure and function in the realm of scientific discovery.

As stated best by renowned organic chemist Dr. John Doe, "The beauty of organic chemistry lies in its vast potential for innovation, where simple molecules can transform into powerful agents of change." This sentiment rings true within the study of compounds such as (3-phenoxyphenyl)methanol.

Synonyms
3-Phenoxybenzyl alcohol
(3-Phenoxyphenyl)methanol
13826-35-2
Benzenemethanol, 3-phenoxy-
3-Phenoxybenzylalcohol
m-Phenoxybenzyl alcohol
3-Phenoxybenzenemethanol
3-(Hydroxymethyl)diphenyl ether
BENZYL ALCOHOL, m-PHENOXY-
1-hydroxymethyl-3-phenoxybenzene
DTXSID7027756
CHEBI:62527
04964J25DQ
DTXCID007756
237-525-1
MFCD00004636
(3-phenoxy-phenyl)-methanol
3-Phenoxylbenzyl alcohol
3-PBOH
(3-phenoxyphenyl)methan-1-ol
3-Phenoxybenzylic alcohol
Permethrin EP Impurity C
CAS-13826-35-2
EINECS 237-525-1
BRN 0475312
mPB-alcohol
UNII-04964J25DQ
4eh7
3-phenoxyphenyl methanol
m-phenoxy-benzyl alcohol
3-phenoxy-benzyl alcohol
[3-(phenoxy)phenyl]methanol
3-06-00-04545 (Beilstein Handbook Reference)
SCHEMBL358425
SCHEMBL473301
(3-(phenyloxy)phenyl)methanol
3-Phenoxybenzyl alcohol, 98%
SCHEMBL6153735
CHEMBL1869836
SCHEMBL11124615
SCHEMBL29661187
DAlc2-H_000047
KGANAERDZBAECK-UHFFFAOYSA-
PHENOXYBENZYL ALCOHOL, 3-
BCP31635
Tox21_201473
Tox21_303571
CK2463
SBB063872
AKOS000249474
CS-W015614
FP71261
PS-4045
NCGC00164079-01
NCGC00164079-02
NCGC00257439-01
NCGC00259024-01
AC-10911
SY036130
DB-042421
NS00000278
P0979
ST50319446
C19800
EN300-1868884
3-Phenoxybenzyl alcohol, purum, >=97.5% (GC)
3-Phenoxybenzyl alcohol;(3-Phenoxyphenyl)methanol
Q18409953
0OO
InChI=1/C13H12O2/c14-10-11-5-4-8-13(9-11)15-12-6-2-1-3-7-12/h1-9,14H,10H2