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S-(-)-2-fluorodecanol | 127608-48-4

中文名称
——
中文别名
——
英文名称
S-(-)-2-fluorodecanol
英文别名
(S)-2-fluoro-1-decanol;2-(S)-fluorodecan-1-ol;2-(S)-fluorodecanol;(2S)-2-fluorodecan-1-ol
S-(-)-2-fluorodecanol化学式
CAS
127608-48-4
化学式
C10H21FO
mdl
——
分子量
176.275
InChiKey
SJZQQJOIMGMRKP-JTQLQIEISA-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):
    3.9
  • 重原子数:
    12
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 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:
    描述:
    S-(-)-2-fluorodecanol硝酸sodium acetate 作用下, 以 溶剂黄146 为溶剂, 生成 (S)-2-fluorodecanoic acid
    参考文献:
    名称:
    Nakamura, S.; Nohira, H., Molecular Crystals and Liquid Crystals (1969-1991), 1990, vol. 185, p. 199 - 207
    摘要:
    DOI:
  • 作为产物:
    描述:
    (R)-1,2-环氧癸烷氟化氢吡啶 作用下, 以 乙醚 为溶剂, 以51%的产率得到S-(-)-2-fluorodecanol
    参考文献:
    名称:
    Nohira, H.; Nakamura, S.; Kamei, M., Molecular Crystals and Liquid Crystals (1969-1991), 1990, vol. 180, p. 379 - 388
    摘要:
    DOI:
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文献信息

  • Enantioselective alpha-fluorination of aldehydes using chiral organic catalysts
    申请人:MacMillan W.C. David
    公开号:US20060189830A1
    公开(公告)日:2006-08-24
    Nonmetallic, chiral organic catalysts are used to catalyze enantioselective fluorination of enolizable aldehydes. Reaction systems composed of an enolizable aldehyde, an electrophilic fluorination reagent, and a nonmetallic chiral catalyst in the form of an imidazolidinone salt are also provided.
    非金属手性有机催化剂被用于催化不对称选择性氟化烯醇醛。由烯醇醛、亲电性氟化试剂和非金属手性催化剂(以咪唑啉酮盐形式)组成的反应体系也被提供。
  • Difluorophenyl pyrimidyl pyridine derivatives and the use thereof in
    申请人:Hoescht Research & Technology Deutchland GmbH & Co.
    公开号:US06022492A1
    公开(公告)日:2000-02-08
    Difluorophenylpyrimidylpyridine derivatives of the formula (I) ##STR1## wherein X is N and Y is CH or X is CH and Y is N; R.sup.1 and R.sup.2 are identical or different and are a) an unbranched or branched alkyl chain having 1 to 20 carbon atoms, where aa) one or more non-adjacent and non-terminal CH.sub.2 groups may be replaced by --O--, --CO--O--, --O--CO--, --O--CO--O-- or --Si(CH.sub.3).sub.2 --, and/or ab) one or more H atoms may be replaced by F, and/or ac) the terminal CH.sub.3 group may be replaced by one of the following chiral groups (optically active or racemic): ##STR2## R.sup.3, R.sup.4 and R.sup.5 are identical or different and are hydrogen or a straight-chain or branched alkyl radical having 1-16 carbon atoms (with or without an asymmetrical carbon atom), where, in addition, one or more non-adjacent non-terminal CH.sub.2 groups may be replaced by --O--, and/or where one or more H atoms of the alkyl radical may be substituted by --F; R.sup.4 and R.sup.5 may alternatively together be --(CH.sub.2).sub.4 -- or --(CH.sub.2).sub.5 -- if they are bonded to a dioxolane system, are suitable as components, in particular, of ferroelectric liquid-crystal mixtures.
    公式(I)的二氟苯基嘧啶基吡啶衍生物,其中X为N,Y为CH或者X为CH,Y为N;R.sup.1和R.sup.2相同或不同,为a)具有1至20个碳原子的直链或支链烷基链,其中aa)一个或多个非相邻和非末端CH.sub.2基团可以被--O--,--CO--O--,--O--CO--,--O--CO--O--或--Si(CH.sub.3).sub.2--取代,和/或ab)一个或多个H原子可以被F取代,和/或ac)末端CH.sub.3基团可以被以下手性基团之一取代(光学活性或外消旋):R.sup.3,R.sup.4和R.sup.5相同或不同,为氢或者具有1-16个碳原子的直链或支链烷基基团(带或不带不对称碳原子),此外,一个或多个非相邻非末端CH.sub.2基团可以被--O--取代,和/或烷基基团的一个或多个H原子可以被--F取代;如果它们与二氧杂环丙烷系统结合,则R.sup.4和R.sup.5可以替代地共同为--(CH.sub.2).sub.4--或--(CH.sub.2).sub.5--,特别适用于铁电液晶混合物的组分。
  • Fluorinated naphthalene derivatives and their use in liquid crystal mixtures
    申请人:Aventis Reseach & Technologies GmbH & Co. KG
    公开号:US06491989B1
    公开(公告)日:2002-12-10
    Fluorinated naphthalene derivatives of the formula (I) R1(—A1—M1)a(—A2—M2)b—B—(—M3—A3)c—(M4—A4)d—R2  (I) where B is  having the meaning  and R1(—A1—M1)a(—A2—M2) and (—M3—A3)(M4—A4)R2 are mesogenic radicals, are suitable as components of liquid-crystal mixtures, in particular ferroelectric liquid-crystal mixtures.
    公式(I)的氟化萘衍生物 其中B具有以下含义,R1(—A1—M1)a(—A2—M2)和(—M3—A3)(M4—A4)R2是向列相基团,适用于液晶混合物的组分,特别是铁电液晶混合物。
  • Optically active silacyclohexane compounds, liquid crystal compositions
    申请人:Shin-Etsu Chemical Co., Ltd.
    公开号:US05730902A1
    公开(公告)日:1998-03-24
    An optically active silacyclohexane compound of the formula (I) ##STR1## wherein R represents an organic residue, X represents --CH.sub.2 -- or --O--; Z represents a chiral group having at least one chiral carbon atom; L.sub.1 and L.sub.2 independently represent H or F, n is 0 or 1; ##STR2## represents a trans-1-sila-1,4-cyclohexylene group or trans-4-sila-1,4-cyclohexylene group whose silicon atom at the 1 or 4 position has H, F, Cl or CH.sub.3, or a 1,4-cyclohexylene group; and ##STR3## represents a trans-1-sila-1,4-cyclohexylene group or trans-4-sila-1,4-cyclohexylene group whose silicon atom at the 1 or 4 position has H, F, Cl or CH.sub.3, a 1,4-cyclohexylene group or a 1,4-phenylene group provided that at least one of ##STR4## represents the trans-1-sila-1,4-cyclohexylene group or trans-4-sila-1,4-cyclohexylene group defined above. A liquid crystal composition comprising the compound defined above and a liquid crystal display device comprising the composition are also described.
    公式(I)表示的是一种光学活性的硅杂环己烷化合物,其中R代表有机残基,X代表-CH.sub.2-或-O-; Z代表具有至少一个手性碳原子的手性基团; L.sub.1和L.sub.2分别表示H或F,n为0或1; ##STR2##表示具有H、F、Cl或CH.sub.3的1或4位硅原子的顺-1-硅-1,4-环己基或顺-4-硅-1,4-环己基或1,4-环己基; 和##STR3##表示具有H、F、Cl或CH.sub.3的1或4位硅原子的顺-1-硅-1,4-环己基或顺-4-硅-1,4-环己基或1,4-环己基或1,4-苯基,前提是至少有一个##STR4##表示上述定义的顺-1-硅-1,4-环己基或顺-4-硅-1,4-环己基。还描述了一种包含上述化合物的液晶组合物和包含该组合物的液晶显示装置。
  • Isoxazole derivatives, and their use in liquid-crystalline mixtures
    申请人:Clariant International Ltd.
    公开号:US06616989B1
    公开(公告)日:2003-09-09
    Isoxazole derivatives of the formula (I) where the symbols and indices have the following meanings, for example: T is X is S or O R1 and R2 are identical or different and are each hydrogen, F, CN or a straight-chain or branched C1-C20-alkyl or C2-C20-alkenyl radical (with or without asymmetric carbon atoms), A1 and A2 are undirected and identical or different and are each phenylene-1,4-diyl, M1 is undirected and is —OC(═O)—, —OCH2—, —SC(═O)—, —SCH2—, —CH2CH2—, —OC(═O)CH2CH2—, —OCH2CH2CH2—, —C≡C—, —(CH2)4— or a single bond; a is 0 or 1, are used in liquid-crystal mixtures.
    式(I)的异噁唑衍生物,其中符号和指数具有以下含义,例如:T为X为S或OR1,R2相同或不同,且每个为氢、F、CN或直链或支链的C1-C20烷基或C2-C20烯基基团(带或不带不对称碳原子);A1和A2为无定向的,相同或不同,且每个为苯基-1,4-二基;M1为无定向的,为—OC(═O)—、—OCH2—、—SC(═O)—、—SCH2—、—CH2CH2—、—OC(═O)CH2CH2—、—OCH2CH2CH2—、—C≡C—、—(CH2)4—或单键;a为0或1,用于液晶混合物。
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