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Catalog Number:
34806
CAS Number:
101-49-5
2-Benzyl-1,3-dioxolane
Purity:
98 - 100% (GC)
Synonym(s):
Phenylacetaldehyde ethylene acetal
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Product Information

2-Benzyl-1,3-dioxolane is a versatile organic compound that serves as a valuable intermediate in the synthesis of various pharmaceuticals and fine chemicals. Its unique structure, featuring a dioxolane ring, enhances its reactivity and makes it an ideal candidate for applications in organic synthesis. Researchers and industry professionals utilize this compound for the development of complex molecules, particularly in the fields of medicinal chemistry and materials science. The compound's ability to undergo various chemical transformations allows for the efficient production of target compounds, making it a preferred choice in laboratories focused on drug discovery and development.

In addition to its synthetic utility, 2-Benzyl-1,3-dioxolane is recognized for its potential in the formulation of specialty chemicals and agrochemicals. Its stability and compatibility with a range of reagents enable its use in diverse chemical reactions, including cycloadditions and rearrangements. This compound not only streamlines the synthesis process but also enhances the overall yield of desired products, providing a significant advantage over similar compounds. With its broad applicability and beneficial properties, 2-Benzyl-1,3-dioxolane is an essential tool for researchers aiming to innovate in their respective fields.

Synonyms
Phenylacetaldehyde ethylene acetal
CAS Number
101-49-5
Purity
98 - 100% (GC)
Molecular Formula
C10H12O2
Molecular Weight
164.2
MDL Number
MFCD00003215
PubChem ID
7562
Appearance
Colorles, oily liquid
Boiling Point
115 - 120 °C at 12 mmHg (Lit.)
Refractive Index
n20/D 1.520 - 1.523
Conditions
Store at RT
General Information
Synonyms
Phenylacetaldehyde ethylene acetal
CAS Number
101-49-5
Purity
98 - 100% (GC)
Molecular Formula
C10H12O2
Molecular Weight
164.2
MDL Number
MFCD00003215
PubChem ID
7562
Appearance
Colorles, oily liquid
Boiling Point
115 - 120 °C at 12 mmHg (Lit.)
Refractive Index
n20/D 1.520 - 1.523
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Benzyl-1,3-dioxolane is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a valuable intermediate in the synthesis of various pharmaceutical agents, enhancing the efficiency of drug formulation processes.
  • Flavor and Fragrance Industry: Its pleasant aromatic properties make it a popular choice in the formulation of perfumes and flavorings, providing a unique scent profile that appeals to consumers.
  • Polymer Chemistry: Used as a monomer or additive, it contributes to the development of specialty polymers, improving material properties such as flexibility and durability.
  • Organic Synthesis: The compound is a key reagent in organic synthesis, facilitating the creation of complex molecules in research laboratories, which is crucial for advancing chemical knowledge.
  • Cosmetic Formulations: Its stability and skin-friendly properties make it an ingredient in cosmetic products, enhancing texture and scent while ensuring safety for users.

Citations