CAS 5234-06-0

2-[(2-Naphthalenyloxy)methyl]oxirane

Description:

2-[(2-Naphthalenyloxy)methyl]oxirane, also known as a glycidyl ether, is an organic compound characterized by the presence of an epoxide functional group and a naphthyl ether moiety. This compound typically appears as a colorless to pale yellow liquid and is known for its reactivity due to the strained three-membered epoxide ring, which can undergo ring-opening reactions in the presence of nucleophiles. The naphthalenyl group contributes to its hydrophobic properties and potential for π-π stacking interactions, which can influence its solubility and reactivity in various solvents. This compound is often utilized in organic synthesis, particularly in the production of polymers and as an intermediate in the synthesis of more complex molecules. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety considerations should be taken into account, as epoxides can be irritants and potentially hazardous. Proper handling and storage conditions are essential to ensure safety during its use in laboratory and industrial settings.

Formula: C₁₃H₁₂O₂

InChI: InChI=1S/C13H12O2/c1-2-4-11-7-12(6-5-10(11)3-1)14-8-13-9-15-13/h1-7,13H,8-9H2

InChI key: InChIKey=BKYSFVJCBRHGMA-UHFFFAOYSA-N

SMILES: O(CC1CO1)C2=CC3=C(C=C2)C=CC=C3

Synonyms:

• (2-Naphthyloxymethyl)oxirane
• (2R)-2-[(naphthalen-2-yloxy)methyl]oxirane
• (2S)-2-[(naphthalen-2-yloxy)methyl]oxirane
• 1-(2-Naphthaleneoxy)-2,3-epoxypropane
• 1-(2-Naphthyloxy)-2,3-epoxypropane
• 2-Glycidyloxynaphthalene
• 2-Naphthyl glycidyl ether
• 2-[(2-Naphthalenyloxy)methyl]oxirane
• 2-[(2-Naphthyloxy)methyl]oxirane
• 2-[(Naphthalen-2-Yloxy)Methyl]Oxirane
• Ai3-13143
• Ccris 2070
• Ether, 2,3-epoxypropyl 2-naphthyl
• Glycidyl 2-Naphthalenyl ether
• Glycidyl 2-naphthyl ether
• Glycidyl beta-naphthyl ether
• Glycidyl β-naphthyl ether
• Naphthalene, 2-(2,3-epoxypropoxy)-
• Naphthalene, 2-(2,3-expoxypropoxy)- (7CI,8CI)
• Oxirane, ((2-naphthalenyloxy)methyl)- (9CI)
• Oxirane, 2-((2-naphthyloxy)methyl)-
• Oxirane, 2-[(2-naphthalenyloxy)methyl]-
• Oxirane, [(2-naphthalenyloxy)methyl]-
• Propane, 1,2-epoxy-3-(2-naphthyloxy)-
• Propane, 1,2-epoxy-3-(2-naphthyloxy)- (6CI)
• [(2-Naphthalenyloxy)methyl]oxirane
• beta-Naphthyl glycidyl ether
• β-Naphthyl glycidyl ether

Propranolol Impurity 9

CAS: 5234-06-0

Formula: C₃H₁₂O₂

Molecular weight: 200.24

Ref: 4Z-P-1624

2-[(naphthalen-2-yloxy)methyl]oxirane

Controlled Product

CAS: 5234-06-0

Applications 2-[(naphthalen-2-yloxy)methyl]oxirane is a monoesters of ibuprofen where are used as prodrugs with analgesic activity
References Soltani Rad. et al., Bioorg. Chem. 107, 104570(2021)

Formula: C₁₃H₁₂O₂

Color and Shape: Neat

Molecular weight: 200.233

Ref: TR-N756923

2-[(Naphthalen-2-yloxy)methyl]oxirane

CAS: 5234-06-0

2-[(Naphthalen-2-yloxy)methyl]oxirane is a monomer that can be used to produce epoxides, amines, and other organic compounds. It is used as a transport agent and catalytic agent for the ring-opening of epoxides. The cyanosilylation reaction of 2-[(naphthalen-2-yloxy)methyl]oxirane with bis[trimethylsilyl]acetamide produces cyanosilylated products. This compound has been shown to be a ligand for phosphazene and polyethers, as well as an effective catalyst in the synthesis of cyclic ethers.

Formula: C₁₃H₁₂O₂

Purity: Min. 95%

Molecular weight: 200.23 g/mol

Ref: 3D-FAA23406

β propranolol epoxide

CAS: 5234-06-0

Formula: C₁₃H₁₂O₂

Molecular weight: 200.24

Ref: ST-EA-CP-P31008