CAS 13107-39-6
:2-(4-Methylphenyl)oxirane
Description:
2-(4-Methylphenyl)oxirane, also known as 4-Methylphenyl glycidyl ether, is an organic compound characterized by its epoxide functional group, which is a three-membered cyclic ether. This compound features a methyl group attached to a phenyl ring, contributing to its aromatic properties. The presence of the oxirane ring imparts significant reactivity, making it susceptible to nucleophilic attack, which is a key feature in various chemical reactions, including ring-opening reactions. It is typically a colorless to pale yellow liquid with a distinctive odor. The compound is used in the synthesis of various polymers and as an intermediate in organic synthesis. Its reactivity and structure make it valuable in the production of epoxy resins and other materials. However, like many epoxides, it may pose health risks, including skin and respiratory irritation, and should be handled with appropriate safety measures. Overall, 2-(4-Methylphenyl)oxirane is an important compound in the field of organic chemistry and materials science.
Formula:C9H10O
InChI:InChI=1S/C9H10O/c1-7-2-4-8(5-3-7)9-6-10-9/h2-5,9H,6H2,1H3
InChI key:InChIKey=QAWJAMQTRGCJMH-UHFFFAOYSA-N
SMILES:CC1=CC=C(C2CO2)C=C1
Synonyms:- (4-Methylphenyl)oxirane
- 2-(4-Methylphenyl)oxirane
- 2-p-Tolyloxirane
- 4-Methylstyrene epoxide
- 4-Methylstyrene oxide
- Brn 0110708
- Ccris 1157
- Oxirane, (4-methylphenyl)-
- Oxirane, 2-(4-methylphenyl)-
- Toluene, p-(epoxyethyl)-
- p-Methylstyrene oxide
- p-Tolyloxirane
- 5-17-01-00591 (Beilstein Handbook Reference)
- See more synonyms
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Found 3 products.
Oxirane, 2-(4-methylphenyl)-
CAS:Formula:C9H10OPurity:95%Color and Shape:LiquidMolecular weight:134.17512-(4-methylphenyl)oxirane
CAS:Controlled Product<p>Applications 2-(4-methylphenyl)oxirane (cas# 13107-39-6) is a useful research chemical.<br></p>Formula:C9H10OColor and Shape:ColourlessMolecular weight:134.172-(4-Methylphenyl)oxirane
CAS:<p>2-(4-Methylphenyl)oxirane (2MPO) is an epoxide that belongs to the group of reactive compounds. It has been shown to react with nucleic acids, forming a covalent linkage with guanosine. 2MPO also reacts with styrene, forming a covalent bond and producing reactive metabolites. The reaction products are hydroxylated by hydroxyl groups on the ring structure, which catalyzes the reaction. Additives can be used to alter the rate of this reaction. 2MPO is also known to react with pluronic F127, forming a covalently linked adduct. This bond is cleaved by hydrolysis in water and exposure to light, releasing 2MPO and regenerating pluronic F127.</p>Formula:C9H10OPurity:Min. 95%Molecular weight:134.17 g/mol


