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- Top rated TRASEOLIDE(68140-48-7)
- Various Specifications TRASEOLIDE(68140-48-7)
- TRASEOLIDE(68140-48-7)
Quick Details
- ProName: Supply high quality TRASEOLIDE(68140-...
- CasNo: 68140-48-7
- Molecular Formula: C18H26O
- Appearance: ask
- Application: ask
- DeliveryTime: Three days later
- PackAge: customer demand
- Port: Shanghai or Qingdao
- ProductionCapacity: 50 Kilogram/Month
- Purity: 94%~99%
- Storage: ask
- Transportation: by sea or by air
- LimitNum: 1 Gram
- Boiling point: 350.0±31.0 °C(Predicted)
- density: 0.933±0.06 g/cm3(Predicted)
Superiority
Details
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 |
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TRASEOLIDE Chemical Properties |
Boiling point | 350.0±31.0 °C(Predicted) |
density | 0.933±0.06 g/cm3(Predicted) |
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) |
Safety Information |
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. |
TRASEOLIDE Preparation Products And Raw materials |