149233
2,6-Dimethyl-2,5-heptadien-4-one
95%
Synonym(s):
Phorone, sym-Diisopropylideneacetone
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About This Item
Linear Formula:
(CH3)2C=CHCOCH=C(CH3)2
CAS Number:
Molecular Weight:
138.21
EC Number:
207-986-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1699751
MDL number:
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vapor density
4.8 (vs air)
vapor pressure
0.38 mmHg ( 20 °C), 1 mmHg ( 42 °C)
assay
95%
refractive index
n20/D 1.497 (lit.)
bp
198-199 °C (lit.)
mp
23-26 °C (lit.)
density
0.885 g/mL at 25 °C (lit.)
SMILES string
C\C(C)=C\C(=O)\C=C(\C)C
InChI
1S/C9H14O/c1-7(2)5-9(10)6-8(3)4/h5-6H,1-4H3
InChI key
MTZWHHIREPJPTG-UHFFFAOYSA-N
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
174.2 °F - closed cup
flash_point_c
79 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Sophie Cazanave et al.
Journal of hepatology, 46(5), 858-868 (2007-02-06)
The agonistic Jo2 anti-Fas antibody reproduces human fulminant hepatitis in mice. We tested the hypothesis that enhancing hepatic glutathione (GSH) stores may prevent Jo2-induced apoptosis. We fed mice with a normal diet or a sulfur amino acid-enriched (SAA(+)) diet increasing
Tom S Chan et al.
Biochemical and biophysical research communications, 317(1), 149-156 (2004-03-30)
Using isolated rat hepatocytes we have shown that glutathione (GSH) depletion by glutathione-S-transferase (GST)-catalyzed conjugation with 1-bromoheptane or phorone was accompanied by a significant elevation in ascorbate synthesis. Glycogenolysis was also stimulated without a significant rise in glucose synthesis. Furthermore
F Bahrami et al.
Chemico-biological interactions, 128(2), 97-113 (2000-10-12)
Previously we reported that methylsulphonyl-2,6-dichlorobenzene, 2, 6-(diCl-MeSO(2)-B), was irreversibly bound to the olfactory mucosa of mice and induced necrosis of the Bowman's glands with subsequent neuroepithelial degeneration and detachment. In this study, autoradiography and histopathology were used to determine tissue-localization
Tom S Chan et al.
Free radical biology & medicine, 38(7), 867-873 (2005-03-08)
Most animals synthesize ascorbate. It is an essential enzymatic cofactor for the synthesis of a variety of biological molecules and also a powerful antioxidant. There is, however, little direct evidence supporting an antioxidant role for endogenously produced ascorbate. Recently, we
Weihong Wang et al.
Organic letters, 14(17), 4486-4489 (2012-08-28)
A chemical investigation of a Korean marine sponge, Phorbas sp., yielded unprecedented sesterterpenoids phorone A (1) and isophorbasone A (2) along with ansellone B (3) and phorbasone A acetate (4). Their complete structures were elucidated by the combination of spectroscopic
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 325929-5G | 04061826715857 |
| 325929-25G | 04061833398333 |
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