- Traseolide 9366993
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- $20.00 / 1KG
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2024-08-15
- CAS:68140-48-7
- Min. Order: 1KG
- Purity: 0.99
- Supply Ability: 20MT/MON
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| TRASEOLIDE Basic information |
Product Name: | TRASEOLIDE | Synonyms: | ATII;5-ACETYL-3-ISOPROPYL-1,1,2,6-TETRAMETHYLINDANE;TRASEOLIDE;1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1h-inden-5-yl]-ethanon;1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl]-Ethanone;Ethanone,1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl]-;Ketone,3-isopropyl-1,1,2,6-tetramethyl-5-indanylmethyl;1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl]ethan-1-one | CAS: | 68140-48-7 | MF: | C18H26O | MW: | 258.4 | EINECS: | 268-799-0 | Product Categories: | Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals | Mol File: | 68140-48-7.mol | |
| TRASEOLIDE Chemical Properties |
Boiling point | 350.0±31.0 °C(Predicted) | density | 0.933±0.06 g/cm3(Predicted) | solubility | Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) | form | Oil to Thick Oil | color | Colourless | Odor | at 100.00 %. dry sweet amber musk herbal creamy | Odor Type | musk | LogP | 5.018 (est) | NIST Chemistry Reference | Ethanone, 1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1h-inden-5-yl]-(68140-48-7) | EPA Substance Registry System | Ethanone, 1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl]- (68140-48-7) |
| TRASEOLIDE Usage And Synthesis |
Chemical Properties | Colourless Oil | Chemical Properties | 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. | Uses | A component of Musk fragrances. | Definition | 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. | Flammability and Explosibility | Not classified |
| TRASEOLIDE Preparation Products And Raw materials |
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