推荐产品
等级
JIS special grade
蒸汽密度
3.4 (vs air)
蒸汽压
3.4 mmHg ( 20 °C)
方案
≥99.0%
表单
liquid
自燃温度
788 °F
expl. lim.
1.1 %, 100 °F
9.4 %
存货情况
available only in Japan
折射率
n20/D 1.450 (lit.)
沸点
155 °C (lit.)
mp
−47 °C (lit.)
密度
0.947 g/mL at 25 °C (lit.)
SMILES字符串
O=C1CCCCC1
InChI
1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2
InChI key
JHIVVAPYMSGYDF-UHFFFAOYSA-N
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警示用语:
Danger
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
111.2 °F
闪点(°C)
44 °C
法规信息
新产品
Application of fragment screening and merging to the discovery of inhibitors of the Mycobacterium tuberculosis cytochrome P450 CYP121.
Sean A Hudson et al.
Angewandte Chemie (International ed. in English), 51(37), 9311-9316 (2012-08-15)
Viktória Fábos et al.
Chemistry, an Asian journal, 7(11), 2629-2637 (2012-09-07)
Iron (and to a lesser extent manganese) in the wall of a 316 stainless steel (SS) reactor is responsible for the hydrogenation of cyclohexanone to cyclohexanol when using an aqueous formic acid solution under high temperature and pressure water (HTPW)
Alakananda Hajra et al.
Organic letters, 14(21), 5488-5491 (2012-10-18)
Dehydrogenative aromatization of cyclohexanone imines to arylamines has been achieved using a palladium catalyst under aerobic conditions. The reaction is applicable to a variety of imines that are either preformed or generated in situ from cyclohexanone derivatives and aryl or
Brahm J Yachnin et al.
Journal of the American Chemical Society, 134(18), 7788-7795 (2012-04-18)
The Baeyer-Villiger monooxygenases (BVMOs) are a family of bacterial flavoproteins that catalyze the synthetically useful Baeyer-Villiger oxidation reaction. This involves the conversion of ketones into esters or cyclic ketones into lactones by introducing an oxygen atom adjacent to the carbonyl
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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