935-04-6 (乙烯氧基甲基-苯,vinyloxymethylbenzene)

CAS号:
935-04-6
中文名称:
乙烯氧基甲基-苯
英文名称:
vinyloxymethylbenzene
分子式:
C9H10O
分子量:
134.175102710724

乙烯氧基甲基-苯(935-04-6)名称与标识符

名称

中文别名:
(乙烯基氧基甲基)苯;乙烯氧基甲基-苯;乙烯基苯甲基醚;
英文别名:
((Vinyloxy)methyl)benzene;(vinyloxymethyl)benzene;Benzene,[(ethenyloxy)methyl]-;ethenoxymethylbenzene;allyl benzyl ether;benzyloxyethylene;Benzylvinylether;ethenoxy-methyl-benzene;vinyl phenylmethyl ether;Benzyl vinyl ether;vinyl benzyl ether;Vinyloxymethylbenzene;[(ethenyloxy)methyl]benzene;MPW87YYN6B;[(vinyloxy)methyl]benzene;vinylbenzyl ether;benzyl-vinyl ether;Vinyloxymethyl-benzene;Benzene, ((ethenyloxy)methyl)-;AZDCYKCDXXPQIK-UHFFFAOYSA-N;NE38828;[(Ethenyloxy)methyl]benzene (ACI);Ether, benzyl vinyl (6CI, 7CI, 8CI);UNII-MPW87YYN6B;Q27284166;AKOS014316067;SB40645;SCHEMBL145091;SCHEMBL13341609;DB-362472;AS-50926;DTXSID90455666;EN300-102076;SY097145;P11489;CS-0049793;935-04-6;MFCD12547209;

标识符

MDL:
MFCD12547209
InChIKey:
AZDCYKCDXXPQIK-UHFFFAOYSA-N
Inchi:
1S/C9H10O/c1-2-10-8-9-6-4-3-5-7-9/h2-7H,1,8H2
SMILES:
O(CC1C=CC=CC=1)C=C

乙烯氧基甲基-苯(935-04-6)物化性质

实验特性

  • LogP : 2.34670
  • PSA : 9.23000
  • 折射率 : 1.51
  • 沸点 : 198.3±19.0 °C at 760 mmHg
  • 蒸气压 : 0.5±0.4 mmHg at 25°C
  • 闪点 : 67.5±12.0 °C
  • 密度 : 1.0±0.1 g/cm3

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 : 134.073164938g/mol
  • 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) : 2.3
  • 拓扑分子极性表面积 : 9.2

乙烯氧基甲基-苯(935-04-6)国际标准相关数据

EINECS:

乙烯氧基甲基-苯(935-04-6)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%

乙烯氧基甲基-苯(935-04-6)合成路线

合成路线:1 步
反应条件:
参考文献:
Electron-transfer reduction of selected alcohols with alkalide K-, K+(15-crown-5)2 via organometallic intermediates
Grobelny, Zbigniew; Stolarzewicz, Andrzej; Maercker, Adalbert; Krompiec, Stanislaw; Kasperczyk, Janusz; et al, Journal of Organometallic Chemistry, 2004, 689(14), 2361-2367
合成路线:1 步
反应条件:
参考文献:
Decomposition of vinyl ethers by alkalide K-, K+(15-crown-5)2 via organopotassium intermediates
Grobelny, Zbigniew; Stolarzewicz, Andrzej; Maercker, Adalbert; Krompiec, Stanislaw; Kasperczyk, Janusz; et al, Journal of Organometallic Chemistry, 2004, 689(9), 1580-1585
合成路线:1 步
反应条件:
参考文献:
Synthesis of Allyl and Alkyl Vinyl Ethers Using an in Situ Prepared Air-Stable Palladium Catalyst. Efficient Transfer Vinylation of Primary, Secondary, and Tertiary Alcohols
Bosch, Martin; Schlaf, Marcel, Journal of Organic Chemistry, 2003, 68(13), 5225-5227
合成路线:1 步
反应条件:
参考文献:
Method for preparing bilastine intermediate
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of vinyl ether compounds using transition metal compound catalysts
, European Patent Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Development of a Highly Efficient Catalytic Method for Synthesis of Vinyl Ethers
Okimoto, Yoshio; Sakaguchi, Satoshi; Ishii, Yasutaka, Journal of the American Chemical Society, 2002, 124(8), 1590-1591
合成路线:1 步
反应条件:
参考文献:
Examining the vinyl moiety as a protecting group for hydroxyl (-OH) functionality under basic conditions
Voronin, Vladimir V.; Ledovskaya, Maria S.; Rodygin, Konstantin S.; Ananikov, Valentine P., Organic Chemistry Frontiers, 2020, 7(11), 1334-1342
合成路线:1 步
反应条件:
参考文献:
A solid acetylene reagent with enhanced reactivity: fluoride-mediated functionalization of alcohols and phenols
Werner, Georg; Rodygin, Konstantin S.; Kostin, Anton A.; Gordeev, Evgeniy G.; Kashin, Alexey S.; et al, Green Chemistry, 2017, 19(13), 3032-3041
合成路线:1 步
反应条件:
参考文献:
Synthesis of vinyl ethers of alcohols using calcium carbide under superbasic catalytic conditions (KOH/DMSO)
Matake, Ryosuke; Adachi, Yusuke; Matsubara, Hiroshi, Green Chemistry, 2016, 18(9), 2614-2618
合成路线:1 步
反应条件:
参考文献:
Direct Synthesis of Deuterium-Labeled O -, S -, N -Vinyl Derivatives from Calcium Carbide
Ledovskaya, Maria S.; Voronin, Vladimir V.; Rodygin, Konstantin S.; Posvyatenko, Alexandra V.; Egorova, Ksenia S.; et al, Synthesis, 2019, 51(15), 3001-3013
合成路线:1 步
反应条件:
参考文献:
Process for preparation of 3-(benzyloxy)-1-cyclobutanone
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Process for preparation of vinyl ether compounds
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Au(I) complexes-catalyzed transfer vinylation of alcohols and carboxylic acids
Nakamura, Aki; Tokunaga, Makoto, Tetrahedron Letters, 2008, 49(23), 3729-3732
合成路线:1 步
反应条件:
参考文献:
Trimethyl Phosphite as a Trap for Alkoxy Radicals Formed from the Ring Opening of Oxiranylcarbinyl Radicals. Conversion to Alkenes. Mechanistic Applications to the Study of C-C versus C-O Ring Cleavage
Ding, Bangwei; Bentrude, Wesley G., Journal of the American Chemical Society, 2003, 125(11), 3248-3259
合成路线:1 步
反应条件:
参考文献:
Chemoselective Formal [4+2] Cycloaddition of 3-Hydroxycyclobutanones with Enones
Harada, Kosuke; Nowaki, Aya; Matsuo, Jun-ichi, Asian Journal of Organic Chemistry, 2013, 2(11), 923-926
合成路线:1 步
反应条件:
参考文献:
Preparation of bifunctional compounds for the targeted degradation of androgen receptors
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Polymer-supported β-bromoethyl selenide: An efficient reagent for the synthesis of aryl vinyl ethers
Sheng, Shou-Ri; Liu, Xiao-Ling; Wang, Xiang-Cong; Xin, Qin; Song, Cai-Sheng, Synthesis, 2004, (17), 2833-2836
合成路线:1 步
反应条件:
参考文献:
Selective Approaches to α- and β-Arylated Vinyl Ethers
Domzalska-Pieczykolan, Anna; Funes-Ardoiz, Ignacio; Furman, Bartlomiej ; Bolm, Carsten, Angewandte Chemie, 2022, 61(1),
合成路线:1 步
反应条件:
参考文献:
Cyclopropylboronates and borates as intermediates for coupling reactions, process for preparation thereof by cyclopropanation of vinylboronates with diazo compounds
, World Intellectual Property Organization, , ,

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乙烯氧基甲基-苯(935-04-6)参考资料

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