Merck
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文件

安全信息

241091

Sigma-Aldrich

反式-4-苯基-3-丁烯-2-酮

≥99%

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线性分子式:
C6H5CH=CHCOCH3
CAS号:
1896-62-4
分子量:
146.19
EC 号:
217-587-6
MDL编号:
MFCD00008779
PubChem化学物质编号:
24854463

蒸汽压

0.01 mmHg ( 25 °C)

检测方案

≥99%

形式

solid

bp

260-262 °C (lit.)

mp

39-41 °C (lit.)

溶解性

alcohol: freely soluble(lit.)
benzene: freely soluble(lit.)
chloroform: freely soluble(lit.)
diethyl ether: freely soluble(lit.)
petroleum ether: very slightly soluble(lit.)
water: very slightly soluble(lit.)

SMILES string

CC(=O)\C=C\c1ccccc1

InChI

1S/C10H10O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-8H,1H3/b8-7+

InChI key

BWHOZHOGCMHOBV-BQYQJAHWSA-N

一般描述

当NADPH存在时，反式-4-苯基-3-丁烯-2-酮可与未经处理的大鼠肝微粒体孵育形成作为代谢产物的反式-4-（4-羟苯基）-3-丁烯-2-酮（4-OH-PBO）。

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

230.0 °F

闪点(°C)

> 110 °C

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

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Jiyong Zhang et al.
The Journal of organic chemistry, 71(7), 2918-2921 (2006-03-25)
The first efficient asymmetric synthesis of obolactone 1 has been accomplished in 11 steps and with a 15% overall yield in which Brown's enantioselective allylation reactions and ring-closing metathesis reaction are key steps.
Bin Cao et al.
Organic & biomolecular chemistry, 10(6), 1239-1245 (2011-12-20)
An efficient and easy procedure to synthesize the pyridinyl analogues of dibenzylideneacetone (pyr-dba) was developed by the condensation of substituted nicotinaldehyde and acetone in the presence of K(2)CO(3) in toluene-EtOH-H(2)O solvent system. Structurally diverse pyr-dba, including quinolinyl dba, can be
Toshiyuki Wakimoto et al.
Methods in enzymology, 515, 337-358 (2012-09-25)
Members of the chalcone synthase superfamily of type III polyketide synthases (PKSs) catalyze iterative condensations of CoA thioesters to produce a variety of polyketide scaffolds with remarkable structural diversity and biological activities. The homodimeric type III PKSs share a common
Indrani Mitra et al.
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We have modeled antioxidant activities of hydroxybenzalacetones against lipid peroxidation induced by t-butyl hydroperoxide (pC1), gamma-irradiation (pC2) and also their 1,1-diphenyl-2-picryl hydrazyl (DPPH) free radical scavenging activity (pC3) using quantitative structure-activity relationship technique. The quantitative structure-activity relationship models were developed
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Organic letters, 4(21), 3623-3626 (2002-10-12)
[reaction: see text] Substrate specificities of plant polyketide synthases (PKSs) were investigated using analogues of malonyl-CoA, the extension unit of the polyketide chain elongation reactions. When incubated with methylmalonyl-CoA and 4-coumaroyl-CoA, plant PKSs (chalcone synthase from Scutellaria baicalensis, stilbene synthase
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