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2-fluoro-1-(naphthalen-1-yl)ethanol | 1354542-07-6

中文名称
——
中文别名
——
英文名称
2-fluoro-1-(naphthalen-1-yl)ethanol
英文别名
2-Fluoro-1-(naphthalen-1-yl)ethan-1-ol;2-fluoro-1-naphthalen-1-ylethanol
2-fluoro-1-(naphthalen-1-yl)ethanol化学式
CAS
1354542-07-6
化学式
C12H11FO
mdl
——
分子量
190.217
InChiKey
SWDXEHMSTNIZJR-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    (2-fluoro-1-(naphthalen-1-yl)-2,2-bis(phenylsulfonyl)ethoxy)trimethylsilane 在 sodium dihydrogenphosphate 、 sodium amalgam 、 magnesium溶剂黄146 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 反应 11.0h, 生成 2-fluoro-1-(naphthalen-1-yl)ethanol
    参考文献:
    名称:
    轻松合成α-一氟甲基醇:使用TMSCF(SO 2 Ph)2进行醛的亲核单氟甲基化
    摘要:
    α-氟甲基苯基砜衍生物作为通用的氟甲基化试剂已广泛用于各种反应中。尽管已经使用氟甲基苯基砜或氟双(磺酰基)甲烷实现了醛类的亲核单氟甲基化,但在温和的反应条件下实现简便的操作方案仍然是人们一直追求的目标。现在,我们报告使用α-三甲基甲硅烷基-α-氟双(苯磺酰基)甲烷[TMSCF(SO 2 Ph)2,TFBSM]作为新型单氟甲基化试剂。由催化量的氟化物引发,可以轻松地将试剂添加到各种醛中,从而以高收率提供所需的产物。计算和动力学研究表明,与其他氟甲基硅烷相比,TFBSM中Si-C键具有出色的不稳定性。
    DOI:
    10.1016/j.jfluchem.2011.10.010
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文献信息

  • Acid- and radical-generating agent and method for generating acid and radical
    申请人:FUJIFILM Wako Pure Chemical Corporation
    公开号:US10451967B2
    公开(公告)日:2019-10-22
    It is a subject of the present invention to provide an acid- and radical-generating agent which has high sensitivity to an active energy ray having a wavelength of around 300 to 450 nm, and can exert both high acid-generating performance and high radical-generating performance, and has heat resistance; and a method for generating an acid and a radical. The present invention relates to a compound represented by the general formula (A); an acid- and radical-generating agent comprising the compound; and a method for generating an acid and a radical: wherein n pieces of R1 each independently represent an alkyl group, which may have a specific functional group in the chain, or in which a hydrogen atom may be substituted by a halogen atom; an alkoxy group, in which a hydrogen atom may be substituted by a halogen atom; an aryl group or an aryloxy group, in which a hydrogen atom may be substituted by a halogen atom, an alkyl group or a haloalkyl group; or an arylalkyl group or an arylalkyloxy group, in which a hydrogen atom may be substituted by a halogen atom, an alkyl group or a haloalkyl group; n pieces of R2 and R3 each independently represent a hydrogen atom, an alkyl group or an alkoxycarbonyl group; R4 to R7 each independently represent a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an alkenyl group, an aryl group, an alkoxycarbonyl group, a dialkylamino group or a nitro group; Y represents an oxygen atom, a sulfur atom, or a carbonyl group; n pieces of Z each independently represent a sulfonyl group or an alkoxyphosphoryl group; n represents 1 or 2.
    本发明的一个目的是提供一种对波长约为300至450纳米的活性能量射线具有高灵敏度的酸和自由基生成剂,能够发挥高酸生成性能和高自由基生成性能,并具有耐热性;以及一种生成酸和自由基的方法。本发明涉及一种由通式(A)表示的化合物;包括该化合物的酸和自由基生成剂;以及生成酸和自由基的方法:其中n个R1分别独立表示一种烷基基团,该烷基基团可能在链中具有特定的功能基团,或者氢原子可能被卤原子取代;一种烷氧基团,其中氢原子可能被卤原子取代;一种芳基或芳氧基,其中氢原子可能被卤原子,烷基或卤代烷基取代;或一种芳基烷基或芳基氧基,其中氢原子可能被卤原子,烷基或卤代烷基取代;n个R2和R3分别独立表示氢原子,烷基基团或烷氧羰基团;R4到R7分别独立表示氢原子,卤原子,烷基基团,烷氧基团,烯基基团,芳基,烷氧羰基团,二烷基氨基团或硝基;Y表示氧原子,硫原子或羰基;n个Z分别独立表示磺酰基或烷氧基磷酰基;n表示1或2。
  • ISOXAZOLE DERIVATIVES
    申请人:SANKYO COMPANY LIMITED
    公开号:EP0885891A1
    公开(公告)日:1998-12-23
    The isoxazole derivatives having the following general formula: [wherein R1 represents an optionally substituted aryl group or aromatic heterocyclic group; R2 represents a hydrogen atom, a halogen atom, an optionally substituted alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, a cycloalkenyl group, an alkoxy group, a cyano group, a carboxyl group, an alkanoyl group, an alkoxycarbonyl group or an optionally substituted carbamoyl group; R3 represents an optionally substituted amino group or a saturated heterocyclic group; X represents an oxygen atom or a sulfur atom; n is an integer of from 2 to 6] has an excellent monoamine oxidase inhibitory activity, and is useful as a therapeutic agent or a preventive agent against nervous diseases such as depression.
    具有以下通式的异噁唑衍生物: [其中 R1 代表任选取代的芳基或芳香杂环基团;R2 代表氢原子、卤素原子、任选取代的烷基、烯基、炔基、环烷基、环烯基、烷氧基、氰基、羧基、烷酰基、烷氧羰基或任选取代的氨基甲酰基;R3 代表任选取代的氨基或饱和杂环基团;X 代表氧原子或硫原子;n 为 2 至 6 的整数]具有极佳的单胺氧化酶抑制活性,可用作治疗剂或预防剂,防治抑郁症等神经疾病。
  • Exploiting a “Beast” in Carbenoid Chemistry: Development of a Straightforward Direct Nucleophilic Fluoromethylation Strategy
    作者:Giovanna Parisi、Marco Colella、Serena Monticelli、Giuseppe Romanazzi、Wolfgang Holzer、Thierry Langer、Leonardo Degennaro、Vittorio Pace、Renzo Luisi
    DOI:10.1021/jacs.7b07891
    日期:2017.10.4
    The first direct and straightforward nucleophilic fluoromethylation of organic compounds is reported. The tactic employs a "fleeting" lithium fluorocarbenoid (LiCH2F) generated from commercially available fluoroiodomethane. Precise reaction conditions were developed for the generation and synthetic exploitation of such a labile species. The versatility of the strategy is showcased in ca. 50 examples involving a plethora of electrophiles. Highly valuable chemicals such as fluoroalcohols, fluoroamines, and fluoromethylated oxygenated heterocycles could: be prepared in very good yields through a single synthetic operation. The scalability of the reaction and its application to complex molecular architectures (e.g., steroids) are documented.
  • ACID- AND RADICAL-GENERATING AGENT AND METHOD FOR GENERATING ACID AND RADICAL
    申请人:WAKO PURE CHEMICAL INDUSTRIES, LTD.
    公开号:US20160342084A1
    公开(公告)日:2016-11-24
    It is a subject of the present invention to provide an acid- and radical-generating agent which has high sensitivity to an active energy ray having a wavelength of around 300 to 450 nm, and can exert both high acid-generating performance and high radical-generating performance, and has heat resistance; and a method for generating an acid and a radical. The present invention relates to a compound represented by the general formula (A); an acid- and radical-generating agent comprising the compound; and a method for generating an acid and a radical: wherein n pieces of R 1 each independently represent an alkyl group, which may have a specific functional group in the chain, or in which a hydrogen atom may be substituted by a halogen atom; an alkoxy group, in which a hydrogen atom may be substituted by a halogen atom; an aryl group or an aryloxy group, in which a hydrogen atom may be substituted by a halogen atom, an alkyl group or a haloalkyl group; or an arylalkyl group or an arylalkyloxy group, in which a hydrogen atom may be substituted by a halogen atom, an alkyl group or a haloalkyl group; n pieces of R 2 and R 3 each independently represent a hydrogen atom, an alkyl group or an alkoxycarbonyl group; R 4 to R 7 each independently represent a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an alkenyl group, an aryl group, an alkoxycarbonyl group, a dialkylamino group or a nitro group; Y represents an oxygen atom, a sulfur atom, or a carbonyl group; n pieces of Z each independently represent a sulfonyl group or an alkoxyphosphoryl group; n represents 1 or 2.
  • US6005116A
    申请人:——
    公开号:US6005116A
    公开(公告)日:1999-12-21
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