68140-48-7CC(=O)c1cc2c(cc1C)C(C)(C)C(C)C2C(C)CIMRYETFJNLKUHK-UHFFFAOYSA-NTraseolide is an indane derivative in which the indane skeleton is substituted by geminal methyl groups at C-1, by single methyl groups at C-2 and C-6, by an isopropyl group at C-3 and by an acetyl group at C-6. It is a constituent of musk odorant. It has a role as a fragrance and an odorant receptor agonist. It is a member of indanes, a methyl ketone and an aromatic ketone.
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
Warning
H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 1609 reports by companies from 2 notifications to the ECHA C&L Inventory.
Chemical: Ethanone, 1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl]-
REACH registered substance: 1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl]ethan-1-one (EC: 268-799-0)
Ethanone, 1-2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl-: Does not have an individual approval but may be used under an appropriate group standard
使用A component of Musk fragrances.
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68140-48-7DTXSID9052393CHEMBL4547572CHEBI:63781化学的特性TRASEOLIDE is a musk fragrance that is prepared from toluene and isobutanoyl chloride by a Friedel–Crafts reaction that yields p-tolyl isopropyl ketone; the ketone is reduced to the corresponding alcohol. Chlorination and treatment with 2-methyl-2-butene yield 1 (cipher)- isopropyl-2,3,3,5-tetramethylindane, which gives the title compound through a Friedel–Crafts reaction with acetyl chloride: It is used in perfume compositions for soaps and detergents.
定義ChEBI: An indane derivative in which the indane skeleton is substituted by geminal methyl groups at C-1, by single methyl groups at C-2 and C-6, by an isopropyl group at C-3 and by an acetyl group at C-6. It is a constituent of musk odorant.