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Merck
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文件

246425

Sigma-Aldrich

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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About This Item

线性分子式:
C6H5CH=CHCOCH=CHC6H5
CAS号:
35225-79-7
分子量:
234.29
MDL號碼:
MFCD00004790
分類程式碼代碼:
12352100
PubChem物質ID:
24854806
NACRES:
NA.22

化驗

98%

形狀

solid

mp

104-107 °C (lit.)

溶解度

acetone: soluble(lit.)
alcohol: slightly soluble(lit.)
chloroform: soluble(lit.)
diethyl ether: slightly soluble(lit.)
water: insoluble(lit.)

SMILES 字串

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 密鑰

WMKGGPCROCCUDY-PHEQNACWSA-N

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相关类别

應用

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

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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
Kiyomori A, et al.
Tetrahedron Letters, 40(14), 2657-2660 null
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
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
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

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