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Merck
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Key Documents

C99000

Sigma-Aldrich

Cycloheptanone

99%

동의어(들):

Ketocycloheptane, Ketoheptamethylene, Suberone

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About This Item

Linear Formula:
C7H12(=O)
CAS Number:
Molecular Weight:
112.17
Beilstein:
969823
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

99%

형태

liquid

refractive index

n20/D 1.461 (lit.)

bp

179 °C (lit.)

density

0.951 g/mL at 25 °C (lit.)

SMILES string

O=C1CCCCCC1

InChI

1S/C7H12O/c8-7-5-3-1-2-4-6-7/h1-6H2

InChI key

CGZZMOTZOONQIA-UHFFFAOYSA-N

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관련 카테고리

픽토그램

FlameExclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

131.0 °F

Flash Point (°C)

55 °C

개인 보호 장비

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


시험 성적서(COA)

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문서 라이브러리 방문

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
Takuya Hashimoto et al.
Journal of the American Chemical Society, 131(18), 6614-6617 (2009-04-22)
Insertion of one methylene unit into the C-C bond of cyclohexanones is a potentially useful, straightforward method for the construction of seven-membered carbocycles. An especially appealing but largely unexplored method in this arena is the nucleophilic addition of diazoalkanes to
Avidor Shulman et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 8(1), 229-239 (2002-02-02)
Antibody 38C2 efficiently catalyzes deuterium-exchange reactions at the alpha position of a variety of ketones and aldehydes, including substrates that have a variety of sensitive functional groups. In addition to the regio- and chemoselectivity of these reactions, the catalytic rates
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
K D Holland et al.
Molecular pharmacology, 37(1), 98-103 (1990-01-01)
The convulsant and/or anticonvulsant activity of unsubstituted and mono-alkyl-substituted cyclopentanones and cyclohexanones were examined by testing the ability of these compounds to produce seizures or to inhibit seizures induced by pentylenetetrazol and maximal electroshock in CF-1 mice. In addition, these

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