推荐产品
蒸汽密度
3.4 (vs air)
蒸汽壓力
3.4 mmHg ( 20 °C)
等級
puriss.
化驗
≥99.5% (GC)
expl. lim.
1.1 %, 100 °F
9.4 %
雜質
≤0.2% water (Karl Fischer)
折射率
n20/D 1.450 (lit.)
bp
155 °C (lit.)
mp
−47 °C (lit.)
密度
0.947 g/mL at 25 °C (lit.)
SMILES 字串
O=C1CCCCC1
InChI
1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2
InChI 密鑰
JHIVVAPYMSGYDF-UHFFFAOYSA-N
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说明
价格
訊號詞
Danger
危險分類
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 1
閃點（°F）
111.2 °F - closed cup
閃點（°C）
44 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Aldol Condensation of Cyclohexanone and Synthesis of Acetal or Ketals [J]. J. Jilin
Yiezhi L, et al.
Journal of Jilin University (Science Edition) / Chi Lin Ta Hsueh Hsueh Pao (Li Hsueh Pan ), 2, 021-021 (1989)
194. A synthesis of vitamin a from cyclohexanone.
Attenburrow J, et al.
Journal of the Chemical Society, 1094-1111 (1952)
Huizhen Liu et al.
Science (New York, N.Y.), 326(5957), 1250-1252 (2009-12-08)
Cyclohexanone is an industrially important intermediate in the synthesis of materials such as nylon, but preparing it efficiently through direct hydrogenation of phenol is hindered by over-reduction to cyclohexanol. Here we report that a previously unappreciated combination of two common
Saulo F P Braga et al.
European journal of medicinal chemistry, 71, 282-289 (2013-12-11)
A series of bis-(arylmethylidene)-cycloalkanones was synthesized by cross-aldol condensation. The activity of the compounds was evaluated against amastigotes forms of Trypanosoma cruzi and promastigotes forms of Leishmania amazonensis. The cytotoxicity of the active compounds on uninfected fibroblasts or macrophages was
Yun-Yun Xu et al.
Bioorganic & medicinal chemistry, 21(2), 388-394 (2012-12-19)
A type of novel α,β-unsaturated cyclohexanone analogous, which designed based on the curcumin core structure, have been discovered as potential EGFR inhibitors. These compounds exhibit potent antiproliferative activity in two human tumor cell lines (Hep G2 and B16-F10). Among them
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