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
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)
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
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)
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
Raju Adepu et al.
Organic & biomolecular chemistry, 10(29), 5554-5569 (2012-06-20)
Novel thieno[2,3-d]pyrimidines containing a cyclohexane ring fused with a six- or five-membered heterocyclic moiety along with a benzylic nitrile were designed as potential inhibitors of PDE4. Expeditious synthesis of these compounds was carried out via a multi-step sequence consisting of
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