Detail of > 17283-81-7
- CAS Number:
- 17283-81-7
- Name:
2-Butanone,4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-
- Superlist Name:
- Dihydro-beta-ionone
- Formula:
- C13H22O
- Molecular Structure:
- Synonyms:
- 4-(2,6,6-Trimethyl-1-cyclohexen-1-yl)-2-butanone;7,8-Dihydro-b-ionone;Dihydro-b-ionone;a,b-Dihydro-b-ionone;b-7,8-Dihydroionone;b-Ionone, dihydro-;4-(2,6,6-trimethylcyclohex-1-en-1-yl)butan-2-one;2-butanone, 4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-;4-(2,6,6-Trimethylcyclohex-1-en-1-yl)butan-2-one;
- Molecular Weight:
- 194.31
- Density:
- 0.876 g/cm3
- Melting Point:
- 311 °C(lit.)
- Boiling Point:
- 263.546 °C at 760 mmHg
- Flash Point:
- 93.833 °C
- Hazard Symbols:
Xi; 
N- Risk Codes:
- 38-51/53
- Safety:
- 61Details
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Reference
- Studies on the constituents of the absolute from flower of Osmanthus fragrans (Gui Hua)
- Studies on the constituents of the absolute from flower of Osmanthus fragrans (Gui Hua). Wen, Guangyu; Yu, Fenglan; Wang, Huating; Kang, Zhiquan; Jiang, Ke; Bian, Yaming (Inst. Bot., Acad. Sin., Beijing, Peop. Rep. China). Zhiwu Xuebao, 25(5), 468-71 (Chinese) 1983. CODEN: CHWHAY.Several substances with their cas registry numbers 620-17-7 and 78-70-6 may be metioned in this study. ISSN: 0577-7496. DOCUMENT TYPE: Journal CA Section: 62 (Essential Oils and Cosmetics) Section cross-reference(s): 17 O. fragrans Flower abs. for use as perfumes or flavors contained trans-linalool oxide [11063-78-8], cis-linalool oxide [11063-77-7], a-ionone [127-41-3], b-ionone [79-77-6], nerol [106-25-2], linalool [78-70-6], geraniol [106-24-1], g-decalactone [706-14-9], 1-hexanol [111-27-3], megastigma-6,8-diene 2,5-oxide [89354-17-6], nonanol [28473-21-4], dihydro-b-ionone [17283-81-7], Et palmitate [628-97-7], 1,2-dimethylbenzene [95-47-6], 6-methyl-5-hepten-2-one [110-93-0], 3-hexenyl formate [2315-09-5], a-terpineol [98-55-5], 3,4-dimethylheptane [922-28-1], trans-6-ethenyltetrahydro-2,2,6-trimethylpyran-3-ol [39028-58-5], cis-6-ethenyltetrahydro-2,2,6-trimethylpyran-3-ol [14009-71-3], benzylethanol [122-97-4], 3,7,11-trimethyl-1,6,10-dodecatrien-3-ol [7212-44-4], m-ethylphenol [620-17-7], 9,12-octadecadienol [506-43-4], Me 3-hydroxybenzoate [19438-10-9] and Me 11,14,17-eicosatrienoate [62472-96-2]. The latter 13 compds. have not been previously detected in the flower oil. .
- Thermochemical study of intermediate products in vitamin A synthesis
- Thermochemical study of intermediate products in vitamin A synthesis. Gadzhiev, S. N.; Gubareva, A. I.; Gerasimov, P. A.; Beregovykh, V. V. (Kuzbas. Politekh. Inst., Kemerovo, USSR). Izv. Vyssh. Uchebn. Zaved. 89803-81-6 and 17283-81-7 are also in the experiment., Khim. Khim. Tekhnol., 27(2), 247-8 (Russian) 1984. CODEN: IVUKAR. ISSN: 0579-2991. DOCUMENT TYPE: Journal CA Section: 69 (Thermodynamics, Thermochemistry, and Thermal Properties) Section cross-reference(s): 26 The heats of combustion of intermediate products in vitamin A synthesis were detd. at room temp. and the heats of formation were derived. .
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