Cas no 21190-34-1 ((2-Isopropylphenyl)methanol)

(2-Isopropylphenyl)methanol is a substituted benzyl alcohol derivative featuring an isopropyl group at the ortho position of the phenyl ring. This compound is commonly utilized as an intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its structure allows for further functionalization, making it valuable for constructing complex molecular frameworks. The presence of the hydroxyl group enables reactions such as esterification, etherification, or oxidation, while the isopropyl substituent can influence steric and electronic properties. The compound is typically handled under standard laboratory conditions, with stability suitable for controlled synthetic applications. Proper storage in a cool, dry environment is recommended to maintain integrity.
(2-Isopropylphenyl)methanol structure
(2-Isopropylphenyl)methanol structure
Product Name:(2-Isopropylphenyl)methanol
CAS No:21190-34-1
MF:C10H14O
MW:150.217563152313
MDL:MFCD09999704
CID:859401
PubChem ID:15269897
Update Time:2025-09-24

(2-Isopropylphenyl)methanol Chemical and Physical Properties

Names and Identifiers

    • (2-Isopropylphenyl)methanol
    • (2-propan-2-ylphenyl)methanol
    • 2-ISOPROPYLBENZYL ALCOHOL
    • Benzenemethanol, 2-(1-methylethyl)- (Related Reference)
    • DA-32102
    • o-Isopropylbenzyl alcohol
    • SCHEMBL357956
    • WAA19034
    • BS-27957
    • CS-0210959
    • 21190-34-1
    • DTXSID30570761
    • [2-(Propan-2-yl)phenyl]methanol
    • AKOS006302630
    • SB85203
    • E90352
    • o-i-propylbenzyl alcohol
    • (2-Isopropyl-phenyl)-methanol
    • 2-(1-Methylethyl)benzenemethanol
    • MDL: MFCD09999704
    • Inchi: 1S/C10H14O/c1-8(2)10-6-4-3-5-9(10)7-11/h3-6,8,11H,7H2,1-2H3
    • InChI Key: UTKXDSMWHKPGNZ-UHFFFAOYSA-N
    • SMILES: OCC1C=CC=CC=1C(C)C

Computed Properties

  • Exact Mass: 150.10452
  • 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: 2.2
  • Topological Polar Surface Area: 20.2?2

Experimental Properties

  • PSA: 20.23

(2-Isopropylphenyl)methanol Pricemore >>

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Additional information on (2-Isopropylphenyl)methanol

Introduction to (2-Isopropylphenyl)methanol (CAS No. 21190-34-1)

(2-Isopropylphenyl)methanol, also known by its CAS registry number CAS No. 21190-34-1, is a versatile organic compound with significant applications in various industries. This compound, characterized by its unique chemical structure, has garnered attention in recent years due to its potential in pharmaceuticals, fragrances, and specialty chemicals. The molecule consists of a methanol group attached to a 2-isopropylphenyl ring, which contributes to its distinctive properties and reactivity.

Recent studies have highlighted the importance of (2-Isopropylphenyl)methanol in the synthesis of bioactive compounds. Researchers have explored its role as an intermediate in the production of pharmaceutical agents, particularly in the development of new drug candidates with improved efficacy and reduced side effects. The compound's ability to undergo various chemical transformations, such as oxidation and esterification, makes it a valuable building block in organic synthesis.

The synthesis of CAS No. 21190-34-1 has been optimized through advanced catalytic methods, enhancing its production efficiency and sustainability. Green chemistry approaches, including the use of biocatalysts and solvent-free conditions, have been employed to minimize environmental impact while maintaining high yields. These advancements underscore the compound's importance in modern chemical manufacturing.

In the fragrance industry, (2-Isopropylphenyl)methanol is recognized for its pleasant odor profile, making it a popular ingredient in perfumes and personal care products. Its aromatic properties are derived from the isopropyl group attached to the phenyl ring, which imparts a unique scent that is both refreshing and long-lasting.

Recent research has also focused on the application of CAS No. 21190-34-1 in materials science. The compound has been used as a precursor for the synthesis of advanced polymers and coatings with enhanced mechanical and thermal properties. Its ability to form stable bonds with other monomers makes it a promising candidate for developing high-performance materials.

The global market for (2-Isopropylphenyl)methanol has seen steady growth due to increasing demand from pharmaceuticals, fragrances, and specialty chemicals sectors. Key players in the industry are investing in R&D to explore new applications and improve production processes further. This trend is expected to continue as the compound's versatility continues to drive innovation across multiple industries.

In conclusion, (2-Isopropylphenyl)methanol (CAS No. 21190-34-1) is a multifaceted compound with a wide range of applications and ongoing research potential. Its role as an intermediate in pharmaceutical synthesis, its use in fragrances, and its emerging applications in materials science highlight its significance in contemporary chemistry. As technology advances and new discoveries emerge, this compound is poised to play an even greater role in shaping future innovations.

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