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Merck
CN

175161

2,2-二甲基-6,6,7,7,8,8,8-七氟-3,5-辛二酮

98%

别名:

6,6,7,7,8,8,8-七氟-2,2-二甲基-3,5-辛二酮

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关于此项目

线性分子式:
CF3CF2CF2COCH2COC(CH3)3
化学文摘社编号:
分子量:
296.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-556-6
Beilstein/REAXYS Number:
2056991
MDL number:
Assay:
98%
Form:
liquid
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assay

98%

form

liquid

impurities

0.1% 4,4′-methylenebis(2,6-di-tert-butylphenol)

refractive index

n20/D 1.379 (lit.)

bp

46-47 °C/5 mmHg (lit.)

density

1.273 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)C(=O)CC(=O)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C10H11F7O2/c1-7(2,3)5(18)4-6(19)8(11,12)9(13,14)10(15,16)17/h4H2,1-3H3

InChI key

SQNZLBOJCWQLGQ-UHFFFAOYSA-N

Application

6,6,7,7,8,8,8-Heptafluoro-2,2-dimethyl-3,5-octanedione (2,2-Dimethyl-6,6,7,7,8,8,8-heptafluoro-3,5-octanedione) was used as a co-inducer in the production of human γ interferon (HuIFN-γ). It was also used as a beta-diketone chelating agent in the extraction of supercritical carbon dioxide.


pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

127.4 °F - closed cup

flash_point_c

53 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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M Deleers et al.
Chemistry and physics of lipids, 33(1), 11-20 (1983-07-01)
The beta-diketone 1,1,1,2,2,3,3-heptafluoro-7,7-dimethyloctane-4,6-dione (FOD) translocates calcium from an aqueous medium into an organic phase. FOD is less efficient than but acts synergistically with A23187 in causing calcium translocation. The FOD-mediated process of calcium translocation is inhibited by NaCl, although the
B D Gomperts et al.
European journal of biochemistry, 117(3), 559-562 (1981-07-01)
We show that the relatively simple beta-diketone, 1.1.1.2.2.3.3-heptafluoro-7,7-dimethyloctane-4,6-dione, known as "fod", will solvate Ca2+ ions in an organic phase. In consequence it will transport Ca2+ across phospholipid bilayers. It acts as predicted for a Ca2+-transporting ionophore in two biological systems:
A Kreutzberger et al.
Arzneimittel-Forschung, 31(2), 288-290 (1981-01-01)
Since in the compound class of 2-ureidopyrimidines accessible through condensation of guanidinecarboxamide (1) with beta-diketones, representatives occur possessing hypnotic activity, the range of applicability of this synthesis on the one hand and the properties of the end products as related



全球贸易项目编号

货号GTIN
175161-5G04061836682804