Description

1-Methylindene (CAS 767-59-9) is a high-purity organic compound with the molecular formula C₁₀H₁₀, widely utilized in chemical synthesis and material science research. This aromatic hydrocarbon, also known as 1-methyl-1H-indene, features a reactive indene core substituted with a methyl group at the 1-position, making it a versatile intermediate for polymerization, ligand design, and specialty chemical production. Our product is rigorously tested to ensure optimal purity and consistency, meeting the stringent requirements of academic, industrial, and pharmaceutical researchers. Available in scalable quantities with detailed technical documentation, 1-Methylindene is ideal for applications demanding precise molecular control.

Properties

• CAS Number: 767-59-9
• Complexity: 146
• IUPAC Name: 1-methyl-1H-indene
• InChI: InChI=1S/C10H10/c1-8-6-7-9-4-2-3-5-10(8)9/h2-8H,1H3
• InChI Key: LRTOHSLOFCWHRF-UHFFFAOYSA-N
• Exact Mass: 130.078250319
• Molecular Formula: C10H10
• Molecular Weight: 130.19
• SMILES: CC1C=CC2=CC=CC=C12
• Monoisotopic Mass: 130.078250319
• Physical Description: Colorless liquid;
• Synonyms: 1-Methyl-1H-indene, 1-METHYLINDENE, 767-59-9, 1H-Indene, 1-methyl-, METHYLINDENE, 1H-Indene, methyl-, .alpha.-Methylindene, Methyl-1H-indene, XEL55RNS7J, 29036-25-7, EINECS 212-185-7, EINECS 249-382-2, NSC-38857, DTXSID50865464, NSC 38857, 1Methylindene, Methyl1Hindene, alpha-Methylindene, 1HIndene, methyl, 1HIndene, 1methyl, DTXCID10220873, DTXSID301026294, 1-METHYLINDENE, (+-)-, 212-185-7, 249-382-2, inchi=1/c10h10/c1-8-6-7-9-4-2-3-5-10(8)9/h2-8h,1h, Indene, 1-methyl-, METHYL INDENE, UNII-XEL55RNS7J, MFCD00039585, 1-Methyl-1H-indene #, SCHEMBL186865, SCHEMBL186866, SCHEMBL217947, SCHEMBL217948, SCHEMBL1423738, SCHEMBL2965909, SCHEMBL2970793, SCHEMBL2972285, SCHEMBL2972842, SCHEMBL2973426, NSC38857, 1-METHYLINDENE, (+/-)-, AKOS004907874, FM35323, DB-056128, NS00042549, A1-00157, Q27293807

Application

1-Methylindene serves as a key monomer in the synthesis of specialty polymers and copolymers, particularly those with tailored optical or electronic properties. It is also employed in organic catalysis and as a precursor for functionalized indene derivatives in pharmaceutical and agrochemical research. Researchers leverage its reactivity in Diels-Alder reactions and metallocene catalyst systems for advanced material development.

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