139211
Cyclohexyl phenyl ketone
98%
๋์์ด(๋ค):
Benzoylcyclohexane
์กฐ์ง ๋ฐ ๊ณ์ฝ ๊ฐ๊ฒฉ์ ๋ณด๋ ค๋ฉด ๋ก๊ทธ์ธ๋ฅผ ํด๋ฆญํฉ๋๋ค.
ํฌ๊ธฐ ์ ํ
์ ํ์ ๋ณด (DICE ๋ฐฐ์ก ์ ๋น์ฉ ๋ณ๋)
Linear Formula:
C6H11COC6H5
CAS ๋ฒํธ:
Molecular Weight:
188.27
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-923-5
Beilstein/REAXYS Number:
2046712
MDL number:
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๋์ ๋ฌธ์์ ํ ์ด๋ฆ
Cyclohexyl phenyl ketone, 98%
InChI key
BMFYCFSWWDXEPB-UHFFFAOYSA-N
InChI
1S/C13H16O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1,3-4,7-8,12H,2,5-6,9-10H2
SMILES string
O=C(C1CCCCC1)c2ccccc2
assay
98%
form
solid
mp
55-57 ยฐC (lit.)
functional group
ketone
phenyl
Quality Level
์ ์ฌํ ์ ํ์ ์ฐพ์ผ์ญ๋๊น? ๋ฐฉ๋ฌธ ์ ํ ๋น๊ต ์๋ด
๊ด๋ จ ์นดํ ๊ณ ๋ฆฌ
Application
Cyclohexyl phenyl ketone was used to investigate the crosslinked cyclohexyl phenyl compounds under thermal and aquathermal conditions. It was used to examine the effects of molecular changes in the benzophenone molecule on phototoxic behavior.
Biochem/physiol Actions
Cyclohexyl phenyl ketone induces photohaemolysis after exposure to ultraviolet A-rich irradiation in human erythrocytes.
์ ์ฅ ๋ฑ๊ธ
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 ยฐF - closed cup
flash_point_c
113 ยฐC - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
๊ฐ์ฅ ์ต์ ๋ฒ์ ์ค ํ๋๋ฅผ ์ ํํ์ธ์:
์ด ์ ํ์ ์ด๋ฏธ ๊ฐ์ง๊ณ ๊ณ์ญ๋๊น?
๋ฌธ์ ๋ผ์ด๋ธ๋ฌ๋ฆฌ์์ ์ต๊ทผ์ ๊ตฌ๋งคํ ์ ํ์ ๋ํ ๋ฌธ์๋ฅผ ์ฐพ์๋ณด์ธ์.
Aqueous organic chemistry. 2. Crosslinked cyclohexyl phenyl compounds.
Siskin M, et al.
Energy and Fuels, 4(5), 482-488 (1990)
Jose Serrano et al.
Xenobiotica; the fate of foreign compounds in biological systems, 50(2), 192-208 (2019-03-20)
1. Cyclic phenones are chemicals of interest to the USEPA due to their potential for endocrine disruption to aquatic and terrestrial species.2. Prior to this report, there was very limited information addressing metabolism of cyclic phenones by fish species and
Marianne Placzek et al.
Acta dermato-venereologica, 93(1), 30-32 (2012-09-18)
Benzophenone is a phototoxic compound with absorption maxima in the ultraviolet A (UVA) and ultraviolet B (UVB) range. Many benzophenone derivatives are known to be photosensitizing. On the other hand, 2-hydroxy-4-methoxybenzophenone is used as a photoprotective agent. The aim of
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