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Bisoprolol

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Identification
Molecular formula
C18H31NO4
CAS number
66722-44-9
IUPAC name
2-[4-(1-hydroxy-1-methyl-ethyl)phenyl]propan-2-ol
State
State

At room temperature, Bisoprolol is generally in solid form, usually as a crystalline powder.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
396.80
Boiling point (Kelvin)
669.95
General information
Molecular weight
325.45g/mol
Molar mass
325.4450g/mol
Density
1.0810g/cm3
Appearence

Bisoprolol is typically a white or off-white crystalline powder.

Comment on solubility

Solubility of 2-[4-(1-hydroxy-1-methyl-ethyl)phenyl]propan-2-ol

The solubility of 2-[4-(1-hydroxy-1-methyl-ethyl)phenyl]propan-2-ol, a complex organic compound, is primarily influenced by its molecular structure and the functional groups present. This compound exhibits moderate solubility in polar solvents due to its hydroxyl (-OH) group, which can engage in hydrogen bonding with the solvent molecules.

Key factors affecting solubility include:

  • Polarity: The presence of the hydroxyl group enhances the polarity of the molecule, facilitating interactions with polar solvents like water.
  • Hydrogen Bonding: The ability to form hydrogen bonds provides an additional driving force for solubility in aqueous environments.
  • Molecular Size: Larger organic structures can exhibit lower solubility due to steric hindrance and reduced interaction with the solvent.
  • Temperature: Increased temperature generally enhances solubility, allowing for better dissolution of organic compounds in suitable solvents.

In summary, while 2-[4-(1-hydroxy-1-methyl-ethyl)phenyl]propan-2-ol is soluble in polar solvents, its solubility may be limited in non-polar environments. Ultimately, the balance between hydrophilic and hydrophobic properties dictates its behavior in different solvents.

Interesting facts

Interesting Facts About 2-[4-(1-hydroxy-1-methyl-ethyl)phenyl]propan-2-ol

2-[4-(1-hydroxy-1-methyl-ethyl)phenyl]propan-2-ol is a fascinating organic compound that exhibits remarkable properties and applications. Here are some intriguing aspects of this compound:

  • Pharmaceutical Relevance: This compound belongs to a class of substances often explored for their potential therapeutic effects. Compounds like this one can exhibit biological activity, making them candidates for drug development.
  • Structural Significance: The presence of the hydroxy group in its structure plays a crucial role in determining the compound's reactivity and solubility. Functional groups such as this often dictate the interaction of the molecule with biological systems.
  • Synthetic Complexity: The synthesis of 2-[4-(1-hydroxy-1-methyl-ethyl)phenyl]propan-2-ol can involve multiple steps, showcasing the intricacy of organic chemistry. Understanding the synthetic pathways highlights the skill and creativity required in chemical synthesis.
  • Isomerism: Like many organic compounds, this compound may exhibit isomerism, including enantiomers. The different spatial arrangements can have diverse effects on biological activity, reminding scientists of the importance of chirality in pharmaceuticals.
  • Real-World Applications: Beyond its synthetic intrigue, compounds similar to 2-[4-(1-hydroxy-1-methyl-ethyl)phenyl]propan-2-ol can find applications in various industries, ranging from cosmetics to agricultural chemicals, showcasing the versatility of organic compounds.

In conclusion, the compound 2-[4-(1-hydroxy-1-methyl-ethyl)phenyl]propan-2-ol serves as an excellent example of the complexity and utility of organic chemistry. Its structure provides insights into biological interactions, while its potential applications continue to inspire research and innovation.

Synonyms
2948-46-1
1,4-Bis(2-hydroxy-2-propyl)benzene
P-BIS(2-HYDROXYISOPROPYL)BENZENE
alpha,alpha,alpha',alpha'-Tetramethyl-1,4-benzenedimethanol
HSDB 5907
p-Bis(alpha-hydroxyisopropyl)benzene
EINECS 220-964-8
G785DRB5XH
DTXSID7029247
alpha,alpha'-Dihydroxy-p-diisopropylbenzene
alpha,alpha,alpha',alpha'-Tetramethyl-p-xylylenediol
alpha,alpha,alpha',alpha'-Tetramethyl-p-benzenedimethanol
DTXCID309247
1,4-Benzenedimethanol, alpha,alpha,alpha',alpha'-tetramethyl-
p-Xylene-alpha,alpha'-diol, alpha,alpha,alpha',alpha'-tetramethyl-
1,4-Benzenedimethanol, alpha1,alpha1,alpha4,alpha4-tetramethyl-
P-BIS(2-HYDROXYISOPROPYL)BENZENE [HSDB]
1,4Bis(2hydroxy2propyl)benzene
pBis(alphahydroxyisopropyl)benzene
alpha,alpha'Dihydroxypdiisopropylbenzene
alpha,alpha,alpha',alpha'Tetramethylpxylenediol
alpha,alpha,alpha',alpha'Tetramethylpbenzenedimethanol
alpha,alpha,alpha',alpha'Tetramethyl1,4benzenedimethanol
1,4Benzenedimethanol, alpha,alpha,alpha',alpha'tetramethyl
pXylenealpha,alpha'diol, alpha,alpha,alpha',alpha'tetramethyl
1,4-Benzenedimethanol, .alpha.1,.alpha.1,.alpha.4,.alpha.4-tetramethyl-
inchi=1/c12h18o2/c1-11(2,13)9-5-7-10(8-6-9)12(3,4)14/h5-8,13-14h,1-4h
1,4-BIS(1-METHYL-1-HYDROXYETHYL)BENZENE
1,4-BIS(2-HYDROXYISOPROPYL)BENZENE
2,2'-(1,4-Phenylene)bis(propan-2-ol)
2-[4-(2-hydroxypropan-2-yl)phenyl]propan-2-ol
1,4-Benzenedimethanol, .alpha.,.alpha.,.alpha.',.alpha.'-tetramethyl-
.alpha.,.alpha.'-Dihydroxy-p-diisopropylbenzene
.alpha.,.alpha.,.alpha.',.alpha.'-Tetramethyl-1,4-benzenedimethanol
UNII-G785DRB5XH
MFCD00009827
|A,|A'-Dihydroxy-1,4-diisopropylbenzene
alpha,alpha,alpha',alpha'-Tetramethyl-p-xylene-alpha,alpha'-diol
SCHEMBL196799
CHEMBL3187761
1,4-bis(hydroxyisopropyl) benzene
2,2'-(p-Phenylene)di-2-propanol
Tox21_200476
1'.4'-Dioxy-1.4-diisopropylbenzol
AKOS015912564
1,4-Bis(alpha-hydroxyisopropyl)benzene
2,2'-(1,4-phenylene)dipropan-2-ol
NCGC00248647-01
NCGC00258030-01
CAS-2948-46-1
1,4-Bis(2-hydroxyisopropyl)benzene, 97%
alpha,alpha'-dihydroxy-p-diisopropyl benzene
CS-0128436
D1577
NS00007309
a,a,a',a'-tetramethyl-1,4-benzenedimethanol
alpha,alpha'-Dihydroxy-1,4-diisopropylbenzene
Y14692
AE-562/43460607
2-[4-(1-hydroxy-1-methylethyl)phenyl]-2-propanol
Q27278881
I+/-,I+/-,I+/-',I+/-'-Tetramethyl-1,4-benzenedimethanol