241091
反式-4-苯基-3-丁烯-2-酮
≥99%
登录 查看组织和合同定价。
选择尺寸
关于此项目
线性分子式:
C6H5CH=CHCOCH3
化学文摘社编号:
分子量:
146.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-587-6
MDL number:
Assay:
≥99%
Form:
solid
产品名称
反式-4-苯基-3-丁烯-2-酮, ≥99%
InChI key
BWHOZHOGCMHOBV-BQYQJAHWSA-N
InChI
1S/C10H10O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-8H,1H3/b8-7+
SMILES string
CC(=O)\C=C\c1ccccc1
vapor pressure
0.01 mmHg ( 25 °C)
assay
≥99%
form
solid
bp
260-262 °C (lit.)
mp
39-41 °C (lit.)
solubility
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.)
functional group
ketone
phenyl
Quality Level
General description
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）。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>230.0 °F
flash_point_c
> 110 °C
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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
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.
Ikuro Abe et al.
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
Highly asymmetric Michael addition to alpha,beta-unsaturated ketones catalyzed by 9-amino-9-deoxyepiquinine.
Jian-Wu Xie et al.
Angewandte Chemie (International ed. in English), 46(3), 389-392 (2006-12-13)
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
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持