Cas no 13443-29-3 (2-Oxiranemethanol,2-benzoate)

2-Oxiranemethanol, 2-benzoate is an epoxy-functionalized benzoate ester with applications in polymer chemistry and organic synthesis. Its key advantages include its dual functionality, combining the reactivity of an epoxy group with the stability of a benzoate ester, making it useful as a crosslinking agent or intermediate in resin formulations. The compound exhibits good solubility in common organic solvents, facilitating its incorporation into various reaction systems. Its epoxy moiety enables participation in ring-opening reactions, while the benzoate group offers steric and electronic modulation. This balance of reactivity and stability makes it suitable for controlled polymerization processes and surface modification applications.
2-Oxiranemethanol,2-benzoate structure
2-Oxiranemethanol,2-benzoate structure
Product Name:2-Oxiranemethanol,2-benzoate
CAS No:13443-29-3
MF:C10H10O3
MW:178.184603214264
CID:144730
Update Time:2025-10-28

2-Oxiranemethanol,2-benzoate Chemical and Physical Properties

Names and Identifiers

    • 2-Oxiranemethanol,2-benzoate
    • 2,3-epoxypropyl benzoate
    • oxiran-2-ylmethyl benzoate
    • 1-Benzoyloxy-2,3-epoxy-propan
    • Denacol EX 191
    • EINECS 236-583-5
    • Glycidyl benzoate
    • Monoglycidyl benzoate
    • Oxiranemethanol,benzoate
    • Benzoic acid glycidyl ester
    • Benzoic acid (oxiran-2-yl)methyl ester
    • Inchi: 1S/C10H10O3/c11-10(13-7-9-6-12-9)8-4-2-1-3-5-8/h1-5,9H,6-7H2
    • InChI Key: XRQKARZTFMEBBY-UHFFFAOYSA-N
    • SMILES: O1CC1COC(C1C=CC=CC=1)=O

Computed Properties

  • Exact Mass: 178.06300
  • Monoisotopic Mass: 178.062994
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 4
  • Complexity: 185
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2
  • Topological Polar Surface Area: 38.8

Experimental Properties

  • Density: 1.206
  • Boiling Point: 272.7°Cat760mmHg
  • Flash Point: 109°C
  • Refractive Index: 1.547
  • PSA: 38.83000
  • LogP: 1.24220

2-Oxiranemethanol,2-benzoate Pricemore >>

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2-Oxiranemethanol,2-benzoate Related Literature

Additional information on 2-Oxiranemethanol,2-benzoate

Introduction to 2-Oxiranemethanol,2-benzoate (CAS No. 13443-29-3)

2-Oxiranemethanol,2-benzoate, with the chemical formula C9H8O3 and a CAS number of 13443-29-3, is a significant compound in the field of organic chemistry and pharmaceutical research. This compound belongs to the class of oxirane derivatives, which are widely recognized for their versatile applications in synthetic chemistry and drug development. The presence of both an oxirane ring and a benzoate moiety makes it a particularly interesting molecule for further exploration and utilization.

The structure of 2-Oxiranemethanol,2-benzoate features a highly reactive oxirane group, which is known for its ability to undergo various chemical transformations, including ring-opening reactions with nucleophiles. This reactivity makes it a valuable intermediate in the synthesis of more complex molecules. Additionally, the benzoate group contributes to the compound's solubility in polar organic solvents, facilitating its use in various chemical reactions and processes.

In recent years, there has been growing interest in the applications of oxirane derivatives in pharmaceutical research. The oxirane ring can be functionalized in multiple ways, allowing for the creation of diverse molecular architectures. These modifications have led to the development of novel compounds with potential therapeutic applications. For instance, studies have shown that derivatives of 2-Oxiranemethanol,2-benzoate exhibit interesting biological activities, making them promising candidates for further investigation.

One of the most notable areas where 2-Oxiranemethanol,2-benzoate has shown promise is in the synthesis of bioactive molecules. Researchers have utilized this compound as a building block to create new drugs targeting various diseases. The oxirane ring's ability to undergo nucleophilic substitution reactions allows for the introduction of different functional groups, enabling the design of molecules with specific biological properties. This flexibility has been particularly useful in the development of antimicrobial and anti-inflammatory agents.

The benzoate moiety in 2-Oxiranemethanol,2-benzoate also plays a crucial role in its applications. Benzoic acid derivatives are well-known for their pharmacological properties and have been used in numerous drugs and pharmaceutical formulations. The presence of this group enhances the compound's bioavailability and stability, making it an attractive candidate for drug development. Moreover, the benzoate group can be further modified to improve solubility and metabolic profiles, which are critical factors in drug design.

Recent advancements in synthetic methodologies have further expanded the potential applications of 2-Oxiranemethanol,2-benzoate. New techniques have allowed for more efficient and selective transformations of this compound, enabling researchers to access previously inaccessible molecular structures. These advancements have not only improved the synthesis of existing drugs but also opened up new avenues for drug discovery.

The pharmaceutical industry has been particularly interested in leveraging the unique properties of 2-Oxiranemethanol,2-benzoate for developing novel therapeutics. For example, researchers have explored its use in creating targeted drug delivery systems. The oxirane ring can be incorporated into polymers or nanoparticles designed to release drugs at specific sites within the body. This approach has shown promise in improving treatment efficacy while minimizing side effects.

Another area where 2-Oxiranemethanol,2-benzoate has found utility is in agrochemical research. Oxirane derivatives have been used as intermediates in the synthesis of pesticides and herbicides due to their reactivity and versatility. The benzoate group enhances these compounds' stability and environmental compatibility, making them suitable for agricultural applications.

The future prospects for 2-Oxiranemethanol,2-benzoate are promising as research continues to uncover new applications and synthetic strategies. The combination of its reactive oxirane group and functional benzoate moiety makes it a valuable tool for chemists and pharmacologists alike. As our understanding of its properties grows, so too will its role in advancing chemical research and pharmaceutical development.

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