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1-Indanol

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Identification
Molecular formula
C9H10O
CAS number
Indan-1-ol's CAS number is 938-03-4.
IUPAC name
indan-1-ol
State
State

At room temperature, 1-Indanol is typically a solid. It is often handled in laboratories in crystalline or powder form and is stable under normal conditions.

Melting point (Celsius)
48.00
Melting point (Kelvin)
321.00
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.00
General information
Molecular weight
134.18g/mol
Molar mass
134.1780g/mol
Density
1.0910g/cm3
Appearence

1-Indanol appears as a white to light yellow crystalline solid at room temperature. It is often manufactured in fine powder form and is moderately stable under standard conditions. It is known for its camphor-like odor.

Comment on solubility

Solubility of Indan-1-ol

Indan-1-ol, with the molecular formula C9H10O, is a compound known for its unique structural features. The solubility of this compound can be influenced by several factors, primarily its polar and non-polar characteristics.

Key points regarding the solubility of indan-1-ol include:

  • Polarity: Indan-1-ol possesses a hydroxyl (-OH) group which enhances its polarity, enabling it to engage in hydrogen bonding.
  • Solvent Compatibility: This compound is generally soluble in polar solvents like water and alcohols, while showing limited solubility in non-polar solvents.
  • Temperature Dependence: As with many organic compounds, solubility can increase with temperature, making warmer solvents more effective for dissolving indan-1-ol.

As a result, it can be said that indan-1-ol exhibits moderate solubility in water, and its solubility profile makes it a valuable compound for various applications within organic chemistry.

Interesting facts

Exploring Indan-1-ol

Indan-1-ol is a fascinating compound that continues to garner interest within the fields of organic chemistry and medicinal research. With its unique structure, it serves several important roles, particularly in the synthesis of more complex organic molecules.

Key Characteristics

  • Structure: Indan-1-ol features a fused ring system, which contributes to its distinctive chemical behavior and reactivity.
  • Applications: It is often utilized in the synthesis of pharmaceutical compounds, making it valuable in drug discovery and development.
  • Flavor and Fragrance: Indan-1-ol has a sweet, floral aroma, offering possibilities for its use in the flavor and fragrance industries.

Interesting Properties

Indan-1-ol is noteworthy for several reasons:

  • Reactivity: The alcohol group in its structure allows for various chemical transformations, making it an excellent reagent in organic synthesis.
  • Research Potential: Studies have suggested that indan derivatives may exhibit biological activities, pushing researchers to explore their medicinal properties.

Did You Know?

Despite being a relatively small molecule, indan-1-ol highlights the richness of organic chemistry. As noted in various scientific literature, it exemplifies how even simple compounds can lead to complex syntheses and innovative applications. The phrase "small but mighty" certainly fits indan-1-ol, as it continues to inspire new research and discoveries in both chemistry and pharmacology.

In conclusion, indan-1-ol stands as a prime example of how foundational compounds can support the advancement of science, bridging the gap between basic research and practical applications.

Synonyms
1-INDANOL
2,3-Dihydro-1H-inden-1-ol
6351-10-6
Indan-1-ol
1-Hydroxyhydrindene
1H-Inden-1-ol, 2,3-dihydro-
LHG5BD7LOR
NSC-31258
CHEBI:16697
EINECS 228-755-3
NSC 31258
RASAGILINE METABOLITE, INDANOL
AI3-05996
228-755-3
inchi=1/c9h10o/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10h,5-6h
Indanol
1-Hydroxyindane
1-Hydroxyindan
(+/-)-1-Indanol
36643-74-0
1H-Indenol, 2,3-dihydro-
MFCD00003797
(S)-1-indanol
EINECS 253-146-4
BRN 2042960
1-Indanole
(-)-indanol
UNII-LHG5BD7LOR
1-Indanol, 98%
(+/-)-1-Hydroxyindan
Indan-1-ol (1-Indanol)
SCHEMBL57132
4-06-00-03824 (Beilstein Handbook Reference)
1H-Inden-1-ol,3-dihydro-
CHEMBL4564909
DTXSID10871162
NSC31258
AKOS000121032
AKOS016050359
DS-3145
SY014889
SY275070
SY289024
DB-046717
DB-054500
DB-055342
DB-243601
CS-0017842
H0516
NS00043260
EN300-21659
C01710
I10213
Q27102031