246425
联甲基苯乙烯酮
98%
别名:
1,5-二苯-1,4-戊二烯-3-酮, 反,反-二亚苄基丙酮
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关于此项目
线性分子式:
C6H5CH=CHCOCH=CHC6H5
化学文摘社编号:
分子量:
234.29
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
联甲基苯乙烯酮, 98%
InChI
1S/C17H14O/c18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16/h1-14H/b13-11+,14-12+
SMILES string
O=C(\C=C\c1ccccc1)/C=C/c2ccccc2
InChI key
WMKGGPCROCCUDY-PHEQNACWSA-N
assay
98%
form
solid
mp
104-107 °C (lit.)
solubility
acetone: soluble(lit.)
alcohol: slightly soluble(lit.)
chloroform: soluble(lit.)
diethyl ether: slightly soluble(lit.)
water: insoluble(lit.)
functional group
ketone
phenyl
Quality Level
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Application
反式 -二亚苄基丙酮被用作铜催化的咪唑 N -芳基化反应的添加剂 。
涉及的反应物：
- Nazarov 样环化
- 转移氢化
- Lewis 酸介导的缩合
- 异-Diels-Alder 反应
- 不对称 1,4-加成反应
- Michael 加成反应
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Rahul Balasaheb Aher et al.
Bioorganic & medicinal chemistry letters, 21(10), 3034-3036 (2011-04-16)
A series of dibenzylideneacetones (A1-A12) and some of their pyrazolines (B1-B4) were synthesized and evaluated in vitro for blood stage antiplasmodial properties in Plasmodium falciparum culture using SYBR-green-I fluorescence assay. The compound (1E, 4E)-1,5-bis(3,4-dimethoxyphenyl)penta-1,4-dien-3-one (A9) was found to be the
Regina Appiah-Opong et al.
European journal of medicinal chemistry, 43(8), 1621-1631 (2008-02-06)
Inhibition of cytochrome P450 (CYP) is a major cause of drug-drug interactions. In this work, inhibitory potentials of 33 curcumin analogues, i.e. 2,6-dibenzylidenecyclohexanone (A series), 2,5-dibenzylidenecyclopentanone (B series) and 1,4-pentadiene-3-one (C series) substituted analogues of curcumin towards recombinant human CYP1A2
Kiyomori A, et al.
Tetrahedron Letters, 40(14), 2657-2660 null
Mengchao Cui et al.
Journal of medicinal chemistry, 54(7), 2225-2240 (2011-03-23)
A new and extensive set of dibenzylideneacetone derivatives was synthesized and screened for affinity toward Aβ(1-42) aggregates. Structure-activity relationships revealed the binding of dibenzylideneacetones to be affected by various substituents. The introduction of a substituent group in the ortho position
D Batovska et al.
European journal of medicinal chemistry, 42(1), 87-92 (2006-09-30)
A large series of chalcones were synthesized and studied for activity against Candida albicans. The SAR analysis showed that the antifungal activity was highly dependent on the substitution pattern of the aryl rings and correlated to a large extent with
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