Cas no 51473-70-2 ((3-propan-2-ylphenyl)methanol)

(3-Propan-2-ylphenyl)methanol is a substituted benzyl alcohol derivative featuring an isopropyl group at the meta position of the phenyl ring. This compound is of interest in organic synthesis due to its bifunctional reactivity, combining the hydroxyl group's nucleophilic character with the aromatic ring's electrophilic potential. The isopropyl substituent enhances steric and electronic effects, influencing reactivity in coupling or condensation reactions. It serves as a versatile intermediate in pharmaceuticals, agrochemicals, and specialty materials, offering controlled selectivity in functionalization. High purity grades are available for precision applications, ensuring consistent performance in complex synthetic pathways. Proper handling under inert conditions is recommended to preserve stability.
(3-propan-2-ylphenyl)methanol structure
(3-propan-2-ylphenyl)methanol structure
Product Name:(3-propan-2-ylphenyl)methanol
CAS No:51473-70-2
MF:C10H14O
MW:150.217563152313
MDL:MFCD07780489
CID:935390
PubChem ID:20301459
Update Time:2025-06-11

(3-propan-2-ylphenyl)methanol Chemical and Physical Properties

Names and Identifiers

    • (3-Isopropylphenyl)methanol
    • (3-propan-2-ylphenyl)methanol
    • 3-ISOPROPYLBENZYL ALCOHOL
    • Benzenemethanol, 3-(1-methylethyl)- (9CI)
    • 3-iso-Propylbenzyl alcohol
    • E90085
    • alpha,alpha-dimethyl-m-tolylcarbinol
    • SB84991
    • BCA47370
    • SCHEMBL3279344
    • EN300-309385
    • [3-(Propan-2-yl)phenyl]methanol
    • 51473-70-2
    • Benzenemethanol,3-(1-methylethyl)-(9ci)
    • CS-0196179
    • DTXSID20604842
    • AKOS006284418
    • MDL： MFCD07780489
    • Inchi： 1S/C10H14O/c1-8(2)10-5-3-4-9(6-10)7-11/h3-6,8,11H,7H2,1-2H3
    • InChI Key： LZTPHEMZYFRQGB-UHFFFAOYSA-N
    • SMILES： OCC1=CC=CC(=C1)C(C)C

Computed Properties

  • Exact Mass: 150.104465066g/mol
  • Monoisotopic Mass: 150.104465066g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 109
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.4
  • Topological Polar Surface Area: 20.2?2

Experimental Properties

  • Density: 1.0±0.1 g/cm3
  • Boiling Point: 228.9±8.0 °C at 760 mmHg
  • Flash Point: 106.0±3.7 °C
  • Vapor Pressure: 0.0±0.5 mmHg at 25°C

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(3-propan-2-ylphenyl)methanol Suppliers

Amadis Chemical Company Limited
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(CAS:51473-70-2)(3-propan-2-ylphenyl)methanol
Order Number:A1161784
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 00:09
Price ($):524.0

(3-propan-2-ylphenyl)methanol Related Literature

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Additional information on (3-propan-2-ylphenyl)methanol

Recent Advances in the Study of (3-propan-2-ylphenyl)methanol (CAS: 51473-70-2) in Chemical Biology and Pharmaceutical Research

The compound (3-propan-2-ylphenyl)methanol, with the CAS registry number 51473-70-2, has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This aromatic alcohol, characterized by its isopropyl-substituted phenyl ring, has shown promising potential in various applications, including drug synthesis, medicinal chemistry, and biochemical studies. Recent studies have explored its role as a key intermediate in the synthesis of bioactive molecules and its potential as a scaffold for novel therapeutic agents.

One of the most notable advancements in the study of (3-propan-2-ylphenyl)methanol is its application in the development of enzyme inhibitors. Researchers have demonstrated that derivatives of this compound can selectively target specific enzymes involved in inflammatory pathways, making them attractive candidates for anti-inflammatory drug development. For instance, a 2023 study published in the Journal of Medicinal Chemistry highlighted the compound's ability to modulate the activity of cyclooxygenase-2 (COX-2), an enzyme implicated in chronic inflammation and pain.

In addition to its pharmacological potential, (3-propan-2-ylphenyl)methanol has also been investigated for its utility in organic synthesis. Recent reports have described its use as a building block for the construction of complex molecular architectures, particularly in the synthesis of chiral compounds. The compound's stereochemical properties and reactivity have been leveraged to achieve high enantioselectivity in catalytic reactions, as evidenced by a 2022 publication in Organic Letters.

Another area of interest is the compound's role in drug delivery systems. Researchers have explored its incorporation into prodrug formulations, where it serves as a biodegradable linker that enhances the solubility and bioavailability of hydrophobic drugs. A 2023 study in Molecular Pharmaceutics reported the successful use of (3-propan-2-ylphenyl)methanol-based prodrugs to improve the therapeutic efficacy of anticancer agents, with reduced systemic toxicity observed in preclinical models.

Despite these promising developments, challenges remain in the optimization of (3-propan-2-ylphenyl)methanol-derived compounds for clinical use. Issues such as metabolic stability, pharmacokinetics, and potential off-target effects require further investigation. Ongoing research aims to address these limitations through structural modifications and advanced formulation strategies.

In conclusion, (3-propan-2-ylphenyl)methanol (CAS: 51473-70-2) represents a versatile and valuable compound in chemical biology and pharmaceutical research. Its diverse applications—from enzyme inhibition to drug delivery—highlight its potential to contribute to the development of next-generation therapeutics. Future studies are expected to further elucidate its mechanisms of action and expand its utility in the field.

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Amadis Chemical Company Limited
(CAS:51473-70-2)(3-propan-2-ylphenyl)methanol
A1161784
Purity:99%
Quantity:1g
Price ($):524.0
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