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1,3-Diphenoxypropan-2-ol

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Identification
Molecular formula
C15H16O3
CAS number
35867-75-3
IUPAC name
1,3-diphenoxypropan-2-ol
State
State

At room temperature, 1,3-Diphenoxypropan-2-ol is in a solid state, existing as a crystalline white powder.

Melting point (Celsius)
40.00
Melting point (Kelvin)
313.20
Boiling point (Celsius)
428.70
Boiling point (Kelvin)
701.90
General information
Molecular weight
244.28g/mol
Molar mass
244.2810g/mol
Density
1.1380g/cm3
Appearence

1,3-Diphenoxypropan-2-ol is typically a white crystalline solid or powder. It may appear as fine crystals or granules depending on the preparation and purity.

Comment on solubility

Solubility of 1,3-diphenoxypropan-2-ol

1,3-diphenoxypropan-2-ol, with its molecular formula C17H18O3, displays interesting solubility characteristics that can be influenced by various factors.

Generally, the solubility of this compound can be summarized as follows:

  • Polar Solvents: It is expected to exhibit some degree of solubility in polar solvents such as water due to its hydroxyl (-OH) group.
  • Non-Polar Solvents: 1,3-diphenoxypropan-2-ol is likely to be more soluble in non-polar organic solvents due to its aromatic ring structure.
  • Temperature Effects: Solubility can increase with rising temperatures, which typically enhances molecular interactions in solutions.

As with many organic compounds, the presence of the diphenoxy group contributes significantly to its overall hydrophobic character, which tends to limit its solubility in water. In summary, when evaluating the solubility of 1,3-diphenoxypropan-2-ol, it is crucial to consider the solvent's polarity and the compound's structural nuances. Utilizing the right solvent ensures effective dissolution, making this compound manageable in various applications.

Interesting facts

Interesting Facts about 1,3-Diphenoxypropan-2-ol

1,3-Diphenoxypropan-2-ol is a fascinating compound that falls under the category of alcohols and is characterized by its unique structure and properties. This compound, often referred to in research and industrial applications, captivates scientists for several reasons:

  • Versatile Applications: 1,3-Diphenoxypropan-2-ol has potential uses in pharmaceutical chemistry and as an intermediate in the synthesis of various organic compounds.
  • Biological Relevance: Researchers have investigated its role in improving the bioavailability of certain drugs, making it an exciting compound in medicinal chemistry.
  • Chemical Stability: The presence of two phenoxy groups enhances the stability of this compound, making it resilient under various chemical conditions.
  • Synthetic Pathways: There are multiple synthetic routes to produce 1,3-diphenoxypropan-2-ol, often involving straightforward substitution reactions that highlight the principles of organic synthesis.

The compound's name reflects its structural features, emphasizing the dual phenoxy moieties and their arrangement in a propanol backbone. For students and scientists alike, understanding the implications of such structural elements opens the door to innovative applications and deeper insights into chemical behavior.

In summary, 1,3-diphenoxypropan-2-ol serves not just as a chemical entity but also as a bridge connecting various fields of study, including organic chemistry, pharmacology, and materials science. As research continues, this compound may reveal even more secrets waiting to be uncovered.

Synonyms
1,3-Diphenoxy-2-propanol
622-04-8
Glycerol 1,3-diphenyl ether
1,3-Difenoxy-2-propanol
2-PROPANOL, 1,3-DIPHENOXY-
NSC 6802
1,2,3-Propanetriol, 1,3-diphenyl diether
NSC 71510
UNII-RTO1IF8E7Z
RTO1IF8E7Z
Glyceryl alpha,gamma-diphenyl ether
EINECS 210-718-8
1,3-Diphenyl glyceryl ether
BRN 1882894
Glyceryl .alpha.,.gamma.-diphenyl ether
1,3-Diphenoxy-2-hydroxypropane
AI3-08138
NSC-6802
NSC-71510
Glyceryl 1,3-diphenyl ether
DTXSID80211233
DTXCID80133724
210-718-8
4-06-00-00590 (beilstein handbook reference)
nkcvhiphzciefc-uhfffaoysa-n
1,3-Diphenoxypropan-2-ol
2-Propanol,3-diphenoxy-
WLN: RO1YQ1OR
1,3-Propanetriol, 1,3-diphenyl diether
NCIOpen2_003468
Oprea1_740521
SCHEMBL267463
2-hydroxy-1,3-diphenoxypropane
NSC6802
HMS1577H07
AAA62204
NSC71510
BBL012759
STK756805
AKOS001116657
VS-03496
CS-0270189
EU-0084923
NS00022525
SR-01000517708
SR-01000517708-1
Q27288287
Z87002505