推荐产品
品質等級
化驗
99%
形狀
liquid
折射率
n20/D 1.461 (lit.)
bp
179 °C (lit.)
密度
0.951 g/mL at 25 °C (lit.)
SMILES 字串
O=C1CCCCCC1
InChI
1S/C7H12O/c8-7-5-3-1-2-4-6-7/h1-6H2
InChI 密鑰
CGZZMOTZOONQIA-UHFFFAOYSA-N
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訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral - Flam. Liq. 3
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
131.0 °F
閃點（°C）
55 °C
個人防護裝備
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Brian T Sullivan et al.
Journal of chemical ecology, 47(1), 10-27 (2021-01-07)
We investigated geographic variation in the semiochemistry of major disturbance agents of western North American pine forests, Dendroctonus brevicomis Le Conte and Dendroctonus barberi Hopkins (Coleoptera: Curculionidae: Scolytinae), species separated by the Great Basin in the USA that until recently
R Singh et al.
Current medicinal chemistry. Anti-cancer agents, 3(6), 431-438 (2003-10-08)
A series of naturally occurring and synthetic novel oxapenam (4-oxa-1-azabicyclo[3.2.0] heptan-7-one) derivatives with their antitumor activity and the structure-activity relationship among this class of compounds is reported. Among the synthetic 4-oxa-1-azabicyclo[3.2.0]heptan-7-one having an ester, amide, ether derivatives of hydroxy group
Richmond Sarpong et al.
Journal of the American Chemical Society, 125(45), 13624-13625 (2003-11-06)
A set of mild processes for the conversion of vinyl cyclopropyl diazo ketones to highly functionalized cycloheptadienones and vinyl cyclopentenones by use of a target-inspired tandem Wolff/Cope rearrangement sequence is described. A divergent reaction course of the vinyl cyclopropyl diazo
M Juza
Journal of chromatography. A, 865(1-2), 35-49 (2000-02-16)
A binary test mixture consisting of cyclopentanone and cycloheptanone is used for the performance evaluation of a pilot-scale simulated moving bed unit. The involved adsorption equilibria and the kinetic behavior are discussed in detail. The results of the test runs
Redouane Beniazza et al.
The Journal of organic chemistry, 76(3), 791-799 (2011-01-13)
A short access to homocalystegine analogues silylated at C7 is described. The synthesis involves the desymmetrization of a (phenyldimethylsilyl)methylcycloheptatriene using osmium-mediated dihydroxylation, followed by the diol protection and a cycloaddition involving the remaining diene moiety and an acylnitroso reagent. Additions
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