所有图片(1)
About This Item
线性分子式:
C6H5CH=CHCOCH=CHC6H5
CAS号:
分子量:
234.29
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
98%
表单
solid
mp
104-107 °C (lit.)
溶解性
acetone: soluble(lit.)
alcohol: slightly soluble(lit.)
chloroform: soluble(lit.)
diethyl ether: slightly soluble(lit.)
water: insoluble(lit.)
官能团
ketone
phenyl
SMILES字符串
O=C(\C=C\c1ccccc1)/C=C/c2ccccc2
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+
InChI key
WMKGGPCROCCUDY-PHEQNACWSA-N
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应用
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
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
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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