摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-丁-3-烯基-3-氟苯 | 2248-12-6

中文名称
1-丁-3-烯基-3-氟苯
中文别名
——
英文名称
4-(3-fluorophenyl)but-1-ene
英文别名
4-(3-Fluor-phenyl)-buten-(1);4-(3-Fluorophenyl)-1-butene;1-but-3-enyl-3-fluorobenzene
1-丁-3-烯基-3-氟苯化学式
CAS
2248-12-6
化学式
C10H11F
mdl
——
分子量
150.196
InChiKey
UMKWOKGXBVXLTN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    176.3±9.0 °C(Predicted)
  • 密度:
    0.971±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2903999090

反应信息

  • 作为反应物:
    描述:
    1-丁-3-烯基-3-氟苯联硼酸频那醇酯 在 [Fe(bpy)3][FeBr4] 、 lithium tert-butoxide 作用下, 以 N,N-二甲基乙酰胺甲苯 为溶剂, 反应 12.0h, 生成 2-(1-(3-fluorophenyl)butan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
    参考文献:
    名称:
    [EN] METHODS OF BORYLATION AND USES THEREOF
    [FR] PROCÉDÉS DE BORYLATION ET LEURS UTILISATIONS
    摘要:
    本发明总体上涉及硼化方法及其用途。特别是,本发明提供了一种通过将化合物与硼化合物、Fe预催化剂和质子添加剂接触来硼化烯烃化合物的方法。硼化发生在化合物中电子给体或电子吸引基团的邻近(β)位置。
    公开号:
    WO2021080511A1
  • 作为产物:
    参考文献:
    名称:
    Picosecond radical kinetics. Rate constants for ring openings of 2-aryl-substituted cyclopropylcarbinyl radicals
    摘要:
    The kinetics of ring openings of a series of eight (trans-2-arylcyclopropyl)methyl radicals (1) were studied by indirect kinetic methods using Barton's PTOC esters as radical precursors and reaction with PhSeH as the competition reaction. The substituents were CF3, F, Me, and OMe located on both the para and meta positions of the aromatic ring. Syntheses of the radical precursors and the products of the radical reactions are described. Kinetics were determined between -43 and 25 degrees C in four cases (CF, and OMe substituents) and at 0 and 25 degrees C in the other four cases. The rate constants at 25 degrees C ranged from 1.0 x 10(11) s(-1) (p-CH3) to 4.1 x 10(11) s(-1) (p-CF,). The relatively large acceleration of the p-CF3 group, ca. 2.5 times as fast as the parent system with Ar = Ph, correlates well with Adam's Delta D substituent parameters but not with other radical substituent parameters. These calibrated radical rearrangements provide a new set of ultrafast reactions that can be applied in mechanistic probe studies.
    DOI:
    10.1139/cjc-77-5-6-1123
点击查看最新优质反应信息

文献信息

  • [EN] PREPARATION OF SURFACTANTS VIA CROSS-METATHESIS<br/>[FR] PRÉPARATION DE TENSIOACTIFS PAR MÉTATHÈSE CROISÉE
    申请人:MATERIA INC
    公开号:WO2015126462A1
    公开(公告)日:2015-08-27
    The present invention relates to compositions comprising 2-phenyl linear alkene benzenes or 2-phenyl linear alkene benzene sulfonates or 2-phenyl linear alkylbenzenes or 2-phenyl linear alkylbenzene sulfonates; where the benzene ring is optionally substituted with one or more groups designated R *, where R * is defined herein and to methods for making the same. This invention also relates to compositions, methods of making, use of, and articles of manufacuture comprising 2-ethoxylated hydroxymethylphenyl linear alkyl benzenes or 2-propoxylated hydroxymethylphenyl linear alkyl benzenes.
    本发明涉及包含2-苯基线性烯烃苯或2-苯基线性烯烃苯磺酸盐或2-苯基线性烷基苯或2-苯基线性烷基苯磺酸盐的组合物;其中苯环可以选择性地被一个或多个被指定为R*的基团取代,其中R*在此处被定义,并且涉及制备这些组合物的方法。本发明还涉及包含2-乙氧基羟甲基苯基线性烷基苯或2-丙氧基羟甲基苯基线性烷基苯的组合物、制备方法、使用方法和制造物品。
  • PREPARATION OF SURFACTANTS VIA CROSS-METATHESIS
    申请人:MATERIA, INC.
    公开号:US20160186094A1
    公开(公告)日:2016-06-30
    The present invention relates to compositions comprising alkene benzenes or alkene benzene sulfonates or alkylbenzenes or alkylbenzene sulfonates; methods for making alkene benzenes or alkene benzene sulfonates or alkylbenzenes or alkylbenzene sulfonates; where the benzene ring is optionally substituted with one or more groups designated R*, where R* is defined herein. More particularly, the present invention relates to compositions comprising 2-phenyl linear alkene benzenes or 2-phenyl linear alkene benzene sulfonates or 2-phenyl linear alkylbenzenes or 2-phenyl linear alkylbenzene sulfonates; methods for making 2-phenyl alkene benzenes or 2-phenyl alkene benzene sulfonates or 2-phenyl alkylbenzenes or 2-phenyl alkylbenzene sulfonates; where the benzene ring is optionally substituted with one or more groups designated R*, where R* is defined herein. This invention also relates to compositions, methods of making, use of, and articles of manufacture comprising 2-ethoxylated hydroxymethylphenyl linear alkyl benzenes. This invention also relates to compositions, methods of making, use of, and articles of manufacture comprising 2-propoxylated hydroxymethylphenyl linear alkyl benzenes.
    本发明涉及包含烯烃苯或烯烃苯磺酸盐或烷基苯或烷基苯磺酸盐的组合物;制备烯烃苯或烯烃苯磺酸盐或烷基苯或烷基苯磺酸盐的方法;其中苯环可以选择性地被一个或多个被指定为R*的基团所取代,其中R*在此被定义。更具体地,本发明涉及包含2-苯基线性烯烃苯或2-苯基线性烯烃苯磺酸盐或2-苯基线性烷基苯或2-苯基线性烷基苯磺酸盐的组合物;制备2-苯基烯烃苯或2-苯基烯烃苯磺酸盐或2-苯基烷基苯或2-苯基烷基苯磺酸盐的方法;其中苯环可以选择性地被一个或多个被指定为R*的基团所取代,其中R*在此被定义。本发明还涉及包含2-乙氧基羟甲基苯基线性烷基苯的组合物,制备方法,使用方法和制造物品。本发明还涉及包含2-丙氧基羟甲基苯基线性烷基苯的组合物,制备方法,使用方法和制造物品。
  • PYRIDONE COMPOUND, AND AGRICULTURAL AND HORTICULTURAL FUNGICIDE HAVING THIS AS ACTIVE COMPONENT
    申请人:Mitsui Chemicals Agro, Inc.
    公开号:EP3611164A1
    公开(公告)日:2020-02-19
    Novel compounds controlling plant diseases are provided. Pyridone compounds of the invention are novel and can control plant diseases. The pyridone compounds of the invention encompass compounds of formula (1) and salts thereof.
    本发明提供了控制植物病害的新型化合物。本发明的吡啶酮化合物很新颖,可以控制植物病害。本发明的吡啶酮化合物包括式(1)化合物及其盐类。
  • The Addition of Trichloromethyl Radical to Substituted 3-Phenyl-1-propenes and 4-Phenyl-1-butenes
    作者:Michael M. Martin、Gerald Jay. Gleicher
    DOI:10.1021/ja01056a026
    日期:1964.1
  • PYRAZOLO-TETRAHYDROPYRIDINE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS
    申请人:Actelion Pharmaceuticals Ltd.
    公开号:EP2013209B1
    公开(公告)日:2011-01-19
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐