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Dihydrocoumarin

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Identification
Molecular formula
C9H10O2
CAS number
119-84-6
IUPAC name
2,3-dihydro-1,4-benzodioxin-6-yl(1-piperidyl)methanone
State
State

At room temperature, Dihydrocoumarin exists as a solid.

Melting point (Celsius)
27.00
Melting point (Kelvin)
300.15
Boiling point (Celsius)
298.00
Boiling point (Kelvin)
571.15
General information
Molecular weight
162.18g/mol
Molar mass
162.1840g/mol
Density
1.1960g/cm3
Appearence

Dihydrocoumarin appears as a white to off-white crystalline solid. Its solid form can be characterized by a slightly sweet aroma.

Comment on solubility

Solubility of 2,3-dihydro-1,4-benzodioxin-6-yl(1-piperidyl)methanone (C9H10O2)

The solubility characteristics of 2,3-dihydro-1,4-benzodioxin-6-yl(1-piperidyl)methanone can provide insights into its potential applications and behavior in various environments. It is essential to consider several factors when evaluating the solubility of this compound:

  • Polarity: Chemical structures with polar functional groups tend to have higher solubility in polar solvents, such as water. The presence of hydroxyl groups or other electronegative atoms can enhance solubility.
  • Hydrogen bonding: The ability of the compound to form hydrogen bonds can significantly influence its solubility in organic and aqueous solutions.
  • Hydrophobic regions: Conversely, regions of hydrophobicity can hinder solubility in polar solvents, which must be balanced against any polar aspects of the molecule.
  • Environmental pH: The pH of the solution can affect ionization states and overall solubility, especially in compounds that can exist in charged forms.

In conclusion, the solubility of 2,3-dihydro-1,4-benzodioxin-6-yl(1-piperidyl)methanone may vary considerably depending on the solvent environment, temperature, and pressure. Further empirical studies would be beneficial to elucidate the specific solubility behavior of this compound under various conditions.

Interesting facts

Interesting Facts About 2,3-Dihydro-1,4-benzodioxin-6-yl(1-piperidyl)methanone

2,3-Dihydro-1,4-benzodioxin-6-yl(1-piperidyl)methanone is a fascinating compound that intrigues chemists and researchers alike due to its unique structure and potential applications. Here are some interesting insights:

  • Structural Complexity: This compound features a distinct benzodioxin ring system, which is known for its stability and reactivity. The incorporation of a piperidine moiety enhances its chemical versatility.
  • Pharmacological Potential: Compounds with similar structures to 2,3-dihydro-1,4-benzodioxin derivatives have been studied for their biological activities, including anti-inflammatory, analgesic, and potentially neuroprotective effects.
  • Synthetic Pathways: The synthesis of this compound can be performed through various methods, making it a point of interest in synthetic organic chemistry. Researchers often explore efficient and environmentally friendly routes to create complex organic molecules.
  • Research Applications: As a member of the benzodioxin family, this compound may be valuable in drug discovery, particularly in developing agents that act on the central nervous system or as potential therapeutic agents in cancer treatments.
  • Analytical Studies: The study of 2,3-dihydro-1,4-benzodioxin derivatives often involves advanced analytical techniques such as NMR (nuclear magnetic resonance) and chromatography, making it a staple in organic chemistry laboratories.
  • Future Prospects: Ongoing research may unveil further biological functionalities and industrial applications, making this compound a worthwhile subject for further investigation.

With its unique structure and potential applications, 2,3-dihydro-1,4-benzodioxin-6-yl(1-piperidyl)methanone continues to be a compound of interest, urging chemists to explore its many facets. As the field of medicinal chemistry advances, this compound may play a key role in new therapeutic developments.

Synonyms
215923-54-9
CX546
CX 546
CX-546
(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)(piperidin-1-yl)methanone
2,3-dihydro-1,4-benzodioxin-6-yl(piperidin-1-yl)methanone
1-(1,4-Benzodioxan-6-ylcarbonyl)piperidine
BDP 17
GR 87
2,3-Dihydro-1,4-benzodioxin-7-yl-(1-piperidyl)methanone
BDP-17
PV6YEC8983
GR-87
CX546 (1-(1,4-BENZODIOXAN-6-YLCARBONYL)P
1-(2,3-DIHYDRO-1,4-BENZODIOXINE-6-CARBONYL)PIPERIDINE
Methanone, (2,3-dihydro-1,4-benzodioxin-6-yl)-1-piperidinyl-
Piperidine, 1-((2,3-dihydro-1,4-benzodioxin-6-yl)carbonyl)-
(2,3-Dihydro-1,4-benzodioxin-6-yl)-1-piperidinylmethanone
Lopac-C-271
CBMicro_029090
Cambridge id 5708417
UNII-PV6YEC8983
Lopac0_000394
Oprea1_361155
MLS000108057
SCHEMBL244490
GTPL4166
CHEMBL1255648
DTXSID70175951
1-[(2,3-Dihydro-1,4-benzodioxin-6-yl)carbonyl]piperidine
HMS2184B08
HMS3261O09
BCP23921
Tox21_500394
MFCD01860868
s6804
STK205195
AKOS002821597
CCG-204095
CS-3628
CX-546?
FC20595
LP00394
SDCCGSBI-0028924.P003
CX546, >=98% (HPLC), solid
NCGC00015200-01
NCGC00015200-02
NCGC00015200-03
NCGC00015200-04
NCGC00015200-05
NCGC00015200-11
NCGC00078109-02
NCGC00078109-03
NCGC00261079-01
AS-64449
HY-12505
SMR000104020
BIM-0028924.P001
DB-066568
C-271
EU-0100394
D82284
SR-01000075430
Q5014874
SR-01000075430-1
1-((2,3-dihydro-1,4-benzodioxin-6-yl)carbonyl)-Piperidine
(2,3-Dihydro-1,4-benzodioxin-6-yl)-1-piperidinylmethanone;1-[(2,3-Dihydro-1,4-benzodioxin-6-yl)carbonyl]piperidine;BDP 17