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线性分子式:
C6H4(COCH3)2
化学文摘社编号:
分子量:
162.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
229-842-9
Beilstein/REAXYS Number:
2042511
MDL number:
Assay:
97%
Form:
crystals
产品名称
1,3-二乙酰基苯, 97%
InChI key
VCHOFVSNWYPAEF-UHFFFAOYSA-N
InChI
1S/C10H10O2/c1-7(11)9-4-3-5-10(6-9)8(2)12/h3-6H,1-2H3
SMILES string
CC(=O)c1cccc(c1)C(C)=O
assay
97%
form
crystals
bp
150-155 °C/15 mmHg (lit.)
mp
28-32 °C (lit.)
functional group
ketone
storage temp.
2-8°C
Quality Level
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Application
1,3-Diacetylbenzene was used in the preparation of polyhydroxylated analogs.
General description
1,3-Diacetylbenzene is an δ-diketone. It induces neuropathological changes in the rodent central and peripheral nervous systems.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
M Artico et al.
Journal of medicinal chemistry, 41(21), 3948-3960 (1998-10-10)
Various cinnammoyl-based structures were synthesized and tested in enzyme assays as inhibitors of the HIV-1 integrase (IN). The majority of compounds were designed as geometrically or conformationally constrained analogues of caffeic acid phenethyl ester (CAPE) and were characterized by a
Min-Sun Kim et al.
Toxicology and applied pharmacology, 183(1), 55-65 (2002-09-10)
The gamma-diketone analogs 1,2-diacetylbenzene (1,2-DAB) and 2,5-hexanedione (2,5-HD), but not the delta-diketone 1,3-diacetylbenzene (1,3-DAB) or the beta-diketone 2,4-hexanedione, induce neuropathological changes in the rodent central and peripheral nervous systems. The molecular targets of these neurotoxic aromatic and aliphatic gamma-diketones, and
Tim Goelen et al.
Pest management science, 77(2), 930-938 (2020-09-26)
Recent studies have shown that microorganisms emit volatile compounds that affect insect behaviour. However, it remains largely unclear whether microbes can be exploited as a source of attractants to improve biological control of insect pests. In this study, we used
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