烯丙基苯基醚 | 1746-13-0
中文名称:
烯丙基苯基醚
英文名称:
Allyl Phenyl Ether
CAS No.:
1746-13-0
分子式:
C9 H1 0 O
分子量:
134.175102710724
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:烯丙基苯基醚结构式
名称和标识符
MDL
MFCD00008644
InChIKey
POSICDHOUBKJKP-UHFFFAOYSA-N
Inchi
1S/C9H10O/c1-2-8-10-9-6-4-3-5-7-9/h2-7H,1,8H2
SMILES
C=CCOC1=CC=CC=C1
BRN
1905622
别名信息
- 中文别名 -
烯丙基苯基醚
丙烯基苯基醚
(2-丙烯氧基)苯
苯基烯丙基醚
烯丙基苯醚
苯烯丙醚
苯氧基丙烯
烯丙氧基苯酚
烯丙基苯乙酯
烯丙氧苯
烯丙氧基苯
2-丙烯氧苯
Allyl Phenyl Ether 丙烯基苯基醚
Meso-丁烷-1,2,3,4-四羧酸酐
- 英文别名 -
(Allyloxy)benzene
(2-PROPENYLOXY)BENZENE
ALLYLOXYBENZENE
PHENYL ALLYL ETHER
(2-propenyloxy)-benzen
(prop-2-enyloxy)-benzene
3-Phenoxypropene
Allyl phenoxylate
Ether, allyl phenyl
Phenyl 2-propenyl ether
Phenylpropenyl ether
USAF do-23
3-Phenoxy-1-propene
BENZENE,(2-PROPENYLOXY)-
2-propenoxybenzene
Phenylpropenyl ethe
Phenol allyl ether
Allyl phenyl ether
prop-2-enoxybenzene
usafdo-23
ether,allylphenyl
(2-Propenyloxy)benzene
ALLYL PHENYL ETHER
物化性质
实验特性
LogP
2.25140
PSA
9.23000
折射率
n20/D 1.522(lit.)
水溶性
不溶
沸点
195°C(lit.)
闪点
华氏:145.4 °F 摄氏:63 °C
颜色与性状
无色透明液体。能随水蒸气挥发。
溶解性
溶于乙醇和乙醚,不溶于水。
密度
0.978 g/mL at 25 °C(lit.)
计算特性
精确分子量
134.07300
氢键供体数量
0
氢键受体数量
1
可旋转化学键数量
3
同位素质量
134.073
重原子数量
10
复杂度
92.9
同位素原子数量
0
确定原子立构中心数量
0
不确定原子立构中心数量
0
确定化学键立构中心数量
0
不确定化学键立构中心数量
0
共价键单元数量
1
疏水参数计算参考值(XlogP)
无
互变异构体数量
无
表面电荷
0
拓扑分子极性表面积
9.2A^2
海关数据
海关编码
2909309090
海关数据
中国海关编码:
2909309090
概述:
2909309090 其他芳香醚及其卤化衍生物、磺化、硝化衍生物(包括亚硝化衍生物)。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:5.5%。普通关税:30.0%
申报要素:
品名, 成分含量, 用途
Summary:
2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
相关文献
1.
Synthesis of 2-aryloxy butenoates by copper-catalysed allylic C–H carboxylation of allyl aryl ethers with carbon dioxide
Atsushi Ueno,Masanori Takimoto,Zhaomin Hou Org. Biomol. Chem. 2017 15 2370
2.
Organic synthesis with the most abundant transition metal–iron: from rust to multitasking catalysts
Sujoy Rana,Jyoti Prasad Biswas,Sabarni Paul,Aniruddha Paik,Debabrata Maiti Chem. Soc. Rev. 2021 50 243
3.
The ortho-Claisen rearrangement of phenyl allyl ethers in trifluoroacetic acid
Ulla Svanholm,Vernon D. Parker J. Chem. Soc. Chem. Commun. 1972 645
4.
Photo-impulsive reactions in the electronic ground state without electronic excitation: non-photo, non-thermal chemical reactions
Izumi Iwakura,Atsushi Yabushita,Jun Liu,Kotaro Okamura,Takayoshi Kobayashi Phys. Chem. Chem. Phys. 2012 14 9696
5.
The mechanism of Claisen rearrangement of allyl phenyl ether from the perspective of topological analysis of the ELF
S?awomir Berski,Piotr Durlak New J. Chem. 2016 40 8717
6.
Dihydrobenzofuran production from catalytic tandem Claisen rearrangement–intramolecular hydroaryloxylation of allyl phenyl ethers in subcritical water
Ligang Luo,Chunze Liu,Zhiqiang Hou,Yuanyuan Wang,Liyi Dai RSC Adv. 2014 4 29527
7.
172. The chemical effects of γ-radiation on organic systems. Part VIII. The radiolysis of allyl phenyl ether and certain other ethers
A. F. Everard,G. A. Swan,P. S. Timmons J. Chem. Soc. 1962 918
8.
Palladium-catalyzed decarboxylative O-allylation of phenols with γ-methylidene-δ-valerolactones
Ran Song,Zhendong Lian,Wei Feng,Tianyi Guan,Wen Si,Daoshan Yang,Jian Lv Org. Chem. Front. 2022 9 4365
9.
Palladium-catalyzed anti-Markovnikov oxidative acetalization of activated olefins with iron(iii) sulphate as the reoxidant
Rodney A. Fernandes,Sandhya S. Yadav,Praveen Kumar Org. Biomol. Chem. 2022 20 427
10.
Base-catalysed prototropic rearrangement. Part I. Comparison of the base-catalysed and the metal carbonyl-catalysed isomerisation of allyl ethers
A. J. Hubert,A. Georis,R. Warin,P. Teyssié J. Chem. Soc. Perkin Trans. 2 1972 366
参考资料
Reaxys RN
1905622
Beilstein
6(4)562
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