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1-氯-5-氟戊烷 | 407-98-7

中文名称
1-氯-5-氟戊烷
中文别名
1-氟-5-氯戊烷
英文名称
1-Chloro-5-fluoropentane
英文别名
5-fluoro-1-chloropentane;1-chloro-5-fluoro-pentane;1-Chlor-5-fluor-pentan
1-氯-5-氟戊烷化学式
CAS
407-98-7
化学式
C5H10ClF
mdl
——
分子量
124.586
InChiKey
HMHFNUWREZQHGJ-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:
    132.34°C (estimate)
  • 密度:
    1.0325

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    7
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:dcccb2446d57e292ea7e8bf92123c2b8
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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

反应信息

  • 作为反应物:
    描述:
    1-氯-5-氟戊烷 在 sodium tetrahydroborate 、 sodium iodide 、 cobalt(II) chloride 作用下, 以 甲醇乙醇 为溶剂, 反应 26.0h, 生成 6-氟己胺
    参考文献:
    名称:
    Approaches towards the synthesis of fluoro(cyclo)alkylamines
    摘要:
    The synthesis of fluoro(cyclo)alkylamines 1-amino-6-fluorohexane (1), 1-amino-7-fluoroheptane (2), cis/trans-4-fluorocyclohexylamine (3a,b) and cis-4-fluoromethylcyclohexylamine (4) has been investigated for use as synthons for histamine receptor ligands for use in PET.
    DOI:
    10.1016/s0022-1139(96)03457-4
  • 作为产物:
    描述:
    1,5-二氯戊烷 在 potassium fluoride 、 乙二醇 作用下, 生成 1-氯-5-氟戊烷
    参考文献:
    名称:
    Hoffmann, Journal of Organic Chemistry, 1949, vol. 14, p. 107
    摘要:
    DOI:
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文献信息

  • THE PREPARATION AND SOME CLEAVAGE REACTIONS OF ALKYL AND SUBSTITUTED ALKYL METHANESULPHONATES: THE SYNTHESIS OF FLUORIDES, IODIDES, AND THIOCYANATES
    作者:F. L. M. Pattison、J. E. Millington
    DOI:10.1139/v56-099
    日期:1956.6.1
    Representative esters of methanesulphonic acid were synthesized, and cleaved to form the corresponding fluorides, iodides, and thiocyanates. From this work was developed a convenient laboratory procedure for converting alcohols to fluorides.
    合成了具有代表性的甲磺酸酯,并裂解形成相应的氟化物、碘化物和硫氰酸酯。从这项工作中开发了一种方便的实验室程序,用于将醇转化为氟化物。
  • TOXIC FLUORINE COMPOUNDS: XIX. ω-FLUOROALKYNES
    作者:F. L. M. Pattison、R. E. A. Dear
    DOI:10.1139/v63-380
    日期:1963.10.1
    Some ω-fluoroalkynes have been prepared and shown to be valuable intermediates in the synthesis of rare long-chain ω-fluoro compounds; successful representative reactions, in all of which the C—F bond remained intact, included Grignard reactions, partial and total catalytic hydrogenation, halogenation, and miscellaneous coupling reactions.
    一些 ω-氟炔已被制备出来,并被证明是合成稀有长链 ω-氟化合物的有价值的中间体;成功的代表性反应包括格氏反应、部分和全部催化氢化、卤化和杂项偶联反应,其中 C-F 键保持完整。
  • 3-AMINO-5-PHENYL-5,6-DIHYDRO-2H-[1,4]OXAZINES
    申请人:Andreini Matteo
    公开号:US20110046122A1
    公开(公告)日:2011-02-24
    The present invention relates to 3-Amino-5-phenyl-5,6-dihydro-2H-[1,4]oxazines of formula I having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful in the therapeutic and/or prophylactic treatment of e.g. Alzheimer's disease and type 2 diabetes.
    本发明涉及具有BACE1和/或BACE2抑制活性的化学式I的3-氨基-5-苯基-5,6-二氢-2H-[1,4]噁嗪,以及它们的制备、含有它们的药物组合物以及它们作为治疗活性物质的用途。本发明的活性化合物在治疗和/或预防治疗阿尔茨海默病和2型糖尿病等疾病方面具有用途。
  • [EN] 3-AMINO-5-PHENYL-5,6-DIHYDRO-2H-[1,4]OXAZINE DERIVATIVES<br/>[FR] DÉRIVÉS DE 3-AMINO-5-PHÉNYL-5,6-DIHYDRO-2H-[1,4]OXAZINE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2011020806A1
    公开(公告)日:2011-02-24
    The present invention relates to 3-Amino-5-phenyl-5,6-dihydro-2H-[l,4]oxazine derivatives of formula (I) having BACE1 and/or BACE2 inhibitory activity, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful in the therapeutic and/or prophylactic treatment of e.g. Alzheimer's disease and type 2 diabetes.
    本发明涉及具有BACE1和/或BACE2抑制活性的式(I)的3-氨基-5-苯基-5,6-二氢-2H-[1,4]噁嗪衍生物,其制备方法,含有它们的药物组合物以及它们作为治疗活性物质的用途。本发明的活性化合物在治疗和/或预防治疗阿尔茨海默病和2型糖尿病等疾病方面是有用的。
  • NOVEL METHOD FOR PREPARING AMINOSILANE-BASED COMPOUND
    申请人:LG Chem, Ltd.
    公开号:US20180282353A1
    公开(公告)日:2018-10-04
    The present invention provides a novel method for preparing an aminosilane-based compound, by which an aminosilane-based compound used for preparing a modified and conjugated diene-based polymer which shows excellent affinity with an inorganic filler in a rubber composition and increases dispersibility, may be prepared in high purity and high yield.
    本发明提供了一种新型的制备氨基硅烷基化合物的方法,通过该方法可以制备出用于制备改性和共轭二烯基聚合物的氨基硅烷基化合物,该聚合物在橡胶组合物中与无机填料具有优异的亲和性,并提高了分散性,可以高纯度和高产率地制备。
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