46195
金合欢基丙酮
technical, mixture of stereo isomers, ≥90% (GC)
别名:
6,10,14-三甲基十五碳-5,9,13-三烯-2-酮
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关于此项目
经验公式（希尔记法）:
C18H30O
化学文摘社编号:
分子量:
262.43
EC Number:
212-097-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1781239
MDL number:
Assay:
≥90% (GC)
grade
technical
assay
≥90% (GC)
refractive index
n20/D 1.481
density
0.88 g/mL at 20 °C (lit.)
SMILES string
C\C(C)=C\CCC(C)=CCCC(C)=CCCC(C)=O
InChI
1S/C18H30O/c1-15(2)9-6-10-16(3)11-7-12-17(4)13-8-14-18(5)19/h9,11,13H,6-8,10,12,14H2,1-5H3
InChI key
LTUMRKDLVGQMJU-UHFFFAOYSA-N
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves
法规信息
新产品
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Substrate specificity of undecaprenyl pyrophophate synthetase from Lactobacillus plantarum.
Baba T and Allen Jr CA.
Biochemistry, 17(26), 5598-5604 (1978)
Geonseek Ryu et al.
Archives of pharmacal research, 26(10), 796-799 (2003-11-12)
Two known farnesylacetone derivatives (1 and 2) were isolated from the Korean brown alga Sargassum sagamianum off Jeju Island, Korea. Compounds 1 and 2 were identified as (5E,10Z)-6,10,14-trimethylpentadeca-5,10-dien-2,12-dione and (5E,9E,13E)-6,10,4-trimethyl-pentadeca-5,9,13-trien-2,12-dione, respectively, by comparison with the literature data. Compounds 1 and
Woon-Seob Shin et al.
Vascular pharmacology, 58(4), 299-306 (2013-02-19)
A specific blocker of L-type Ca(2+) channels may be useful in decreasing arterial tone by reducing the open-state probability of L-type Ca(2+) channels. The aim of the present study was to evaluate the farnesylacetones, which are major active constituents of