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1-(Bromomethyl)-2-(fluoromethyl)benzene | 158884-44-7

中文名称
——
中文别名
——
英文名称
1-(Bromomethyl)-2-(fluoromethyl)benzene
英文别名
2-fluoromethylbenzyl bromide
1-(Bromomethyl)-2-(fluoromethyl)benzene化学式
CAS
158884-44-7
化学式
C8H8BrF
mdl
——
分子量
203.054
InChiKey
RAJRLLVWSOVELC-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:
    228.1±20.0 °C(Predicted)
  • 密度:
    1.443±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Intramolecular Reactivity of Arylcarbenes: Derivatives of o-Tolylcarbene
    摘要:
    Various CH(2)X groups have been attached to the ortho position of phenylcarbene. If 2'- or 3'-C-H bonds are present, as in 23 (X = Me), 71 (X = CMe(3)), and 58 (X = SiMe(3)), C-H insertion leading to five- or six-membered rings predominates in the gas phase and competes with intermolecular reactions in solution. The formation of benzocyclobutenes via insertion into 1'-C-H bonds is a very minor reaction path of 23 and 71. In contrast, 58 produces substantial amounts of the benzocyclobutene 59 by way of C-Si insertion, particularly in the gas phase. Insertion into the Si-Me bonds of 58 also occurs while the C-F bonds of 37 (X = CF3) and 50 (X = Fl are inert. In the gas phase, 37 and 50 give mainly benzocyclobutenes whereas intermolecular reactions prevail in solution. The effects of sensitization and of solvent polarity suggest that benzocyclobutenes arise from singlet arylcarbenes. The amount of carbene-carbene rearrangement decreases in the order 7 (X = H) > 37 (X = CF3) > 23 (X = Me); no rearrangement was observed with 50 (X = Fl, 58 (X = SiMe(3)), and 71 (X = CMe(3)).
    DOI:
    10.1021/jo00093a014
  • 作为产物:
    描述:
    1,2-二(溴甲基)苯 在 calcium fluoride 、 potassium fluoride 作用下, 以 乙腈 为溶剂, 反应 90.0h, 以31%的产率得到1-(Bromomethyl)-2-(fluoromethyl)benzene
    参考文献:
    名称:
    Intramolecular Reactivity of Arylcarbenes: Derivatives of o-Tolylcarbene
    摘要:
    Various CH(2)X groups have been attached to the ortho position of phenylcarbene. If 2'- or 3'-C-H bonds are present, as in 23 (X = Me), 71 (X = CMe(3)), and 58 (X = SiMe(3)), C-H insertion leading to five- or six-membered rings predominates in the gas phase and competes with intermolecular reactions in solution. The formation of benzocyclobutenes via insertion into 1'-C-H bonds is a very minor reaction path of 23 and 71. In contrast, 58 produces substantial amounts of the benzocyclobutene 59 by way of C-Si insertion, particularly in the gas phase. Insertion into the Si-Me bonds of 58 also occurs while the C-F bonds of 37 (X = CF3) and 50 (X = Fl are inert. In the gas phase, 37 and 50 give mainly benzocyclobutenes whereas intermolecular reactions prevail in solution. The effects of sensitization and of solvent polarity suggest that benzocyclobutenes arise from singlet arylcarbenes. The amount of carbene-carbene rearrangement decreases in the order 7 (X = H) > 37 (X = CF3) > 23 (X = Me); no rearrangement was observed with 50 (X = Fl, 58 (X = SiMe(3)), and 71 (X = CMe(3)).
    DOI:
    10.1021/jo00093a014
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文献信息

  • BICYCLOAMINE DERIVATIVES
    申请人:Ozaki Fumihiro
    公开号:US20090270369A1
    公开(公告)日:2009-10-29
    Compounds represented by formula (I) and pharmaceutically acceptable salts thereof have excellent sodium channel inhibitory action and are useful as therapeutic agents and analgesics for various kinds of neuralgia, neuropathy, epilepsy, insomnia, premature ejaculation and the like. wherein Q represents ethylene, etc., R 1 , R 2 and R 3 represent hydrogen, etc., X 1 represents C 1-6 alkylene, etc., X 2 represents C 1-6 alkylene, etc., A 1 represents a 5- to 6-membered heterocyclic group, etc., and A 2 represents C 6-14 aryl, etc.
    由式(I)表示的化合物及其药学上可接受的盐具有出色的钠通道抑制作用,并可用作治疗剂和各种神经痛、神经病、癫痫、失眠、早泄等的镇痛剂。其中Q代表乙烯等,R1、R2和R3代表氢等,X1代表C1-6烷基等,X2代表C1-6烷基等,A1代表5-至6-成员杂环基团等,A2代表C6-14芳基等。
  • [EN] HALOALUMINOXANE COMPOSITIONS, THEIR PREPARATION, AND THEIR USE IN CATALYSIS<br/>[FR] COMPOSITIONS D'HALOALUMINOXANE, PREPARATION ET UTILISATION DE CELLES-CI DANS DES CATALYSES
    申请人:ALBEMARLE CORP
    公开号:WO2005066191A1
    公开(公告)日:2005-07-21
    Novel haloaluminoxane compositions have been formed. The halogen is fluorine, chlorine, and/or bromine, and the amount of halogen atoms present in said composition is in the range of about 0.5 mole % to about 15 mole % relative to aluminum atoms.
    已经形成了新的氧化铝卤代铝簇合物。卤素可以是氟、氯和/或溴,而该簇合物中存在的卤素原子的数量在相对于铝原子约0.5摩尔%至约15摩尔%的范围内。
  • Spiro-oxindole compounds and their use as therapeutic agents
    申请人:Xenon Pharmaceuticals Inc.
    公开号:US08263606B2
    公开(公告)日:2012-09-11
    This invention is directed to spiro-oxindole compounds, as stereoisomers, enantiomers, tautomers thereof or mixtures thereof; or pharmaceutically acceptable salts, solvates or prodrugs thereof, for the treatment and/or prevention of sodium channel-mediated diseases or conditions, such as pain.
    本发明涉及螺环-氧吲哚化合物,包括其立体异构体、对映异构体、互变异构体或其混合物;或其药学上可接受的盐、溶剂化物或前药,用于治疗和/或预防钠通道介导的疾病或病状,如疼痛。
  • SPIRO-OXINDOLE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS
    申请人:Chafeev Mikhail
    公开号:US20100137299A1
    公开(公告)日:2010-06-03
    This invention is directed to spiro-oxindole compounds, as stereoisomers, enantiomers, tautomers thereof or mixtures thereof; or pharmaceutically acceptable salts, solvates or prodrugs thereof, for the treatment and/or prevention of sodium channel-mediated diseases or conditions, such as pain.
    本发明涉及螺环氧吲哚化合物,包括其立体异构体、对映异构体、互变异构体或其混合物;或其药学上可接受的盐、溶剂化合物或前药,用于治疗和/或预防钠通道介导的疾病或症状,例如疼痛。
  • SPIRO-OXINDOLE COMPOUNDS AND THEIR USES AS THERAPEUTIC AGENTS
    申请人:Chafeev Mikhail
    公开号:US20120295897A1
    公开(公告)日:2012-11-22
    This invention is directed to spiro-oxindole compounds, as stereoisomers, enantiomers, tautomers thereof or mixtures thereof; or pharmaceutically acceptable salts, solvates or prodrugs thereof, for the treatment and/or prevention of sodium channel-mediated diseases or conditions, such as pain.
    本发明涉及螺环氧吲哚化合物,包括立体异构体、对映体、互变异构体或其混合物;或其药学上可接受的盐、溶剂合物或前药,用于治疗和/或预防钠通道介导的疾病或病症,例如疼痛。
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