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3-butoxy-propyne | 66235-25-4

中文名称
——
中文别名
——
英文名称
3-butoxy-propyne
英文别名
butyl-prop-1-ynyl ether;Butyl-prop-1-inyl-aether;1-Butoxy-proin;1-(1-Propyn-1-yloxy)butane;1-prop-1-ynoxybutane
3-butoxy-propyne化学式
CAS
66235-25-4
化学式
C7H12O
mdl
——
分子量
112.172
InChiKey
TXQYSQNYRDCIEW-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:
    137.2±9.0 °C(Predicted)
  • 密度:
    0.838±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    8
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

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:
    3-butoxy-propyne吡啶五氯化磷 作用下, 以 四氯化碳乙醚 为溶剂, 生成 ((E)-2-Butoxy-2-chloro-1-methyl-vinyl)-phosphonic acid dimethyl ester
    参考文献:
    名称:
    Kazankova,M.A. et al., Journal of general chemistry of the USSR, 1978, vol. 48, p. 58 - 64
    摘要:
    DOI:
  • 作为产物:
    描述:
    2-bromo-1t-butoxy-propene 在 氢氧化钾 作用下, 生成 3-butoxy-propyne
    参考文献:
    名称:
    Nooi; Arens, Recueil des Travaux Chimiques des Pays-Bas, 1959, vol. 78, p. 284,286, 287
    摘要:
    DOI:
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文献信息

  • Phenylalanine enamide derivatives
    申请人:——
    公开号:US20020169336A1
    公开(公告)日:2002-11-14
    Phenylalanine enamide derivatives of formula (1) are described: 1 wherein R 1 is a group Ar 1 L 2 Ar 2 Alk- in which: Ar 1 is an optionally substituted aromatic or heteroaromatic group; L 2 is a covalent bond or a linker atom or group; Ar 2 is an optionally substituted arylene or heteroarylene group; and Alk is a chain —CH 2 —CH(R)13 , —CH═C(R)— or 2 in which R is a carboxylic acid (—CO 2 H) or a derivative or biostere thereof; X is an —O— or —S— atom or —N(R 2 )— group in which: R x , R y and R z which may be the same or different is each a hydrogen atom or an optional substituent; or R z is an atom or group as previously defined and R x and R y are joined together to form an optionally substituted spiro linked cycloaliphatic or heterocycloaliphatic group; and the salts, solvates, hydrates and N-oxides thereof. The compounds are able to inhibit the binding of integrins to their ligands and are of use in the prophylaxis and treatment of immuno or inflammatory disorders or disorders involving the inappropriate growth or migration of cells.
    描述了公式(1)的苯丙氨酸烯酰胺衍生物:其中R1是Ar1L2Ar2Alk-中的一种基团,其中:Ar1是可选择取代的芳香族或杂环芳基;L2是一个共价键或连接原子或基团;Ar2是可选择取代的芳基或杂芳基;Alk是一个链-CH2-CH(R)13,-CH═C(R)-或2其中R是羧酸(-CO2H)或其衍生物或生物立体异构体;X是一个-O-或-S-原子或-N(R2)-基团,其中:Rx、Ry和Rz可能相同也可能不同,分别是氢原子或可选择取代基;或Rz是如前所定义的原子或基团,Rx和Ry结合在一起形成一个可选择取代的螺环联接的环脂肪族或杂环脂肪族基团;以及它们的盐、溶剂合物、水合物和N-氧化物。这些化合物能够抑制整合素与其配体的结合,并可用于预防和治疗免疫或炎症性疾病或涉及细胞不当生长或迁移的疾病。
  • Phenylalanine Enamide Derivatives
    申请人:Brand Stephen
    公开号:US20070167483A1
    公开(公告)日:2007-07-19
    Phenylalanine enamide derivatives of formula (1) are described: wherein R 1 is a group Ar 1 L 2 Ar 2 Alk- in which: Ar 1 is an optionally substituted aromatic or heteroaromatic group; L 2 is a covalent bond or a linker atom or group; Ar 2 is an optionally substituted arylene or heteroarylene group; and Alk is a chain in which R is a carboxylic acid (—CO 2 H) or a derivative or biostere thereof; X is an —O— or —S— atom or —N(R 2 )— group in which: R x , R y and R z which may be the same or different is each a hydrogen atom or an optional substituent; or R z is an atom or group as previously defined and R x and R y are joined together to form an optionally substituted spiro linked cycloaliphatic or heterocycloaliphatic group; and the salts, solvates, hydrates and N-oxides thereof. The compounds are able to inhibit the binding of integrins to their ligands and are of use in the prophylaxis and treatment of immuno or inflammatory disorders or disorders involving the inappropriate growth or migration of cells.
    描述了公式(1)的苯丙氨酸烯酰衍生物:其中R1是Ar1L2Ar2Alk-基团,其中:Ar1是可选的取代芳香族或杂芳族基团;L2是共价键或连接原子或基团;Ar2是可选的取代芳烃或杂芳烃基团;Alk是链,在其中R是羧酸(-CO2H)或其衍生物或生物同分异构体;X是一个-O-或-S-原子或-N(R2)-基团,其中:Rx,Ry和Rz可相同或不同,分别是氢原子或可选的取代基团;或Rz是先前定义的原子或基团,而Rx和Ry结合在一起形成可选的取代螺环脂肪族或杂环脂肪族基团;以及其盐,溶剂化合物,水合物和N-氧化物。这些化合物能够抑制整合素与其配体的结合,并用于预防和治疗免疫或炎症性疾病或涉及细胞不适当生长或迁移的疾病。
  • Method of preparing rubber composition including syndiotactic 1,2-polybutadiene
    申请人:Korea Kumho Petrochemical Co., Ltd.
    公开号:US10711075B2
    公开(公告)日:2020-07-14
    Provided is a method of preparing a rubber composition, which includes (a) reacting a conjugated diene-based monomer with one or more of compounds in the presence of a first catalyst; (b) adding a conjugated diene-based monomer to a product of the step (a) and inducing a reaction; and (c) adding a second catalyst and a conjugated diene-based monomer to a product of the step (b) and inducing a reaction.
    本发明提供了一种制备橡胶组合物的方法,该方法包括:(a) 在第一催化剂存在下,使共轭二烯基单体与一种或多种化合物反应;(b) 向步骤(a)的产物中加入共轭二烯基单体并诱导反应;以及(c) 向步骤(b)的产物中加入第二催化剂和共轭二烯基单体并诱导反应。
  • Efficient Synthesis of 3-Aminocyclobut-2-en-1-ones:  Squaramide Surrogates as Potent VLA-4 Antagonists
    作者:Stephen Brand、Benjamin C. de Candole、Julien A. Brown
    DOI:10.1021/ol034701n
    日期:2003.6.1
    [GRAPHICS]A novel series of uniquely functionalized 3-aminocyclobut-2-en-1-ones has been prepared by facile condensation of a variety of cyclobuta-1,3-diones with a phenylalanine-derived primary amine. These systems subsequently lend themselves to substitution at C-2 by reaction with a variety of electrophilic reagents including N-halosuccinimides, sulfenyl chlorides, and Eschenmoser's salt. Compounds from this novel series are potent antagonists of VLA-4.
  • van Daalen,J.J. et al., Recueil des Travaux Chimiques des Pays-Bas, 1961, vol. 80, p. 810 - 818
    作者:van Daalen,J.J. et al.
    DOI:——
    日期:——
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