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methacrylic acid-(3,3-dimethyl-butyl ester) | 77363-18-9

中文名称
——
中文别名
——
英文名称
methacrylic acid-(3,3-dimethyl-butyl ester)
英文别名
Methacrylsaeure-(3,3-dimethyl-butylester);3,3-Dimethylbutyl 2-methylprop-2-enoate
methacrylic acid-(3,3-dimethyl-butyl ester)化学式
CAS
77363-18-9
化学式
C10H18O2
mdl
——
分子量
170.252
InChiKey
URQYRMNIDDQKKW-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):
    3.7
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • Films and Particles
    申请人:Colson Yolonda
    公开号:US20080075718A1
    公开(公告)日:2008-03-27
    Described herein are compounds and processes that can be used to prepare polymer-based films, particles, gels and related compositions, and processes for delivery of agents, and other uses.
    本文描述了可用于制备基于聚合物的薄膜、颗粒、凝胶及相关组合物的化合物和工艺,以及用于传递药剂和其他用途的工艺。
  • STIMULI-SWITCHABLE MOIETIES, MONOMERS AND POLYMERS INCORPORATING STIMULI-SWITCHABLE MOIETIES, AND METHODS OF MAKING AND USING SAME
    申请人:THE GOVERNORS OF THE UNIVERSITY OF ALBERTA
    公开号:US20170267689A1
    公开(公告)日:2017-09-21
    Stimuli-switchable moieties, monomers incorporating stimuli-switchable moieties, and polymers incorporating such stimuli-switchable moieties are provided. The stimuli-switchable moiety can be a pyrano aryl chromenone-derivative. The stimuli-switchable monomer can be a lactone monomer. The stimuli-switchable monomer can be an amino acid, which can be incorporated into a specific peptide sequence by peptide synthesis.
    提供刺激响应性基团、包含刺激响应性基团的单体以及包含此类刺激响应性基团的聚合物。刺激响应性基团可以是喃并芳基色烯酮衍生物。刺激响应性单体可以是内酯单体。刺激响应性单体可以是氨基酸,其可以通过肽合成并入特定的肽序列中。
  • Aqueous dispersion based of viscous silicone oils crosslinkable by condensation into an adhering elastomer for use in particular as sealants or paints, preparation method
    申请人:——
    公开号:US20040054070A1
    公开(公告)日:2004-03-18
    The invention concerns an aqueous dispersion of viscous silicone oils capable of being crosslinked into an elastomer by water elimination (condensation). The invention aims at obtaining an aqueous silicone dispersion corresponding to an optimal compromise in terms of adherence of the crosslinked elastomer on all types of supports, and the colloidal stability of the dispersion during preparation and storage. Said aqueous dispersion comprises a viscous silicone oil A, optionally a crosslinking agent B, optionally an adhesion promoter C (silane), a filler D, a catalyst E, an emulsifier F, optionally a functional additive G and water. Said dispersion is characterised in that the filler D is input into the process for obtaining the dispersion, in the form of an aqueous suspension of at least a hydrophilic compound (CaCO3SiO2, TiO2, Al2/H2O, organic polymer latex). The invention also concerns the preparation of said particularly stable dispersion since it has a residual emulsion rate T not less than 70%. The invention is useful for producing concentrated sealants and elastomer coating for insulating polymer foam (polyurethane).
    本发明涉及一种粘性有机油的分散体,能够通过消除(缩合)交联成弹性体。本发明旨在获得一种性有机分散体,以在制备和储存期间实现交联弹性体对所有类型支撑物的粘附和分散稳定性的最佳折衷。所述性分散体包括粘性有机油A,可选交联剂B,可选粘附剂C(硅烷),填料D,催化剂E,乳化剂F,可选功能性添加剂G和。所述分散体的特征在于,填料D以至少一种亲化合物(CaCO3SiO2,TiO2,Al2/H2O,有机聚合物乳液)的悬浮液的形式输入到获得分散体的过程中。本发明还涉及制备该特别稳定分散体的方法,因为它具有不少于70%的残留乳化率T。本发明有助于生产浓缩密封剂和用于绝缘聚合物泡沫(聚酯)的弹性体涂层。
  • Immunomodulating Heterocyclic Compounds
    申请人:Matthews Richard Ian
    公开号:US20080045527A1
    公开(公告)日:2008-02-21
    Compounds of formula (I) are inhibitors of CD80 and useful in immunomodulation therapy: wherein R 1 and R 3 independently represent H; F; Cl; Br; —NO 2 ; —CN; C 1 -C 6 alkyl optionally substituted by F or Cl; or C 1 -C 6 alkoxy optionally substituted by F; R 4 represents a carboxylic acid group (—COOH) or an ester thereof, or —C(═O)NR 6 R 7 , —NR 7 C(═O)R 6 , —NR 7 C(═O)OR 6 , —NHC(═O)NR 7 R 6 or —NHC(═S)NR 7 R 6 wherein R 6 represents H, or a radical of formula -(Alk) m -Q wherein m is 0 or 1, Alk is an optionally substituted divalent straight or branched C 1 -C 12 alkylene, or C 2 -C 12 alkenylene, or C 2 -C 12 alkynylene radical or a divalent C 3 -C 12 carbocyclic radical, any of which radicals may contain one or more —O—, —S— or —N(R 8 )— links wherein R 8 represents H or C 1 -C 4 alkyl, C 3 -C 4 alkenyl, C 3 -C 4 alkynyl, or C 3 -C 6 cycloalkyl, and Q represents H; —NR 9 R 10 wherein R 9 and R 10 independently represents H; C 1 -C 4 alkyl; C 3 -C 4 alkenyl; C 3 -C 4 alkynyl; C 3 -C 6 cycloalkyl; an ester group; an optionally substituted carbocyclic or heterocyclic group; or R 9 and R 10 form a ring when taken together with the nitrogen to which they are attached, which ring is optionally substituted; and R 7 represents H or C 1 -C 6 alkyl; or when taken together with the atom or atoms to which they are attached R 6 and R 7 form an optionally substituted monocyclic heterocyclic ring having 5, 6 or 7 ring atoms; and X represents a bond or a divalent radical of formula -(Z) n -(Alk)- or -(Alk)-(Z) n - wherein Z represents —O—, —S— or —NH—, Alk is as defined in relation to R 6 and n is 0 or 1.
    式(I)的化合物是CD80的抑制剂,可用于免疫调节治疗:其中R1和R3分别表示H; F; Cl; Br; -NO2; -CN; C1-C6烷基,其可选地被F或Cl取代; 或C1-C6烷氧基,其可选地被F取代; R4表示羧酸基(-COOH)或其酯,或-C(=O)NR6R7,-NR7C(=O)R6,-NR7C(=O)OR6,-NHC(=O)NR7R6或-NHC(=S)NR7R6,其中R6表示H,或式-(Alk)m-Q的基团,其中m为0或1,Alk为可选地取代的二价直链或支链C1-C12烷基,或C2-C12烯基,或C2-C12炔基基团或二价C3-C12环烷基基团,其中任何基团都可以包含一个或多个-O-,-S-或-N(R8)-链接,其中R8表示H或C1-C4烷基,C3-C4烯基,C3-C4炔基,或C3-C6环烷基; Q表示H; -NR9R10,其中R9和R10独立地表示H; C1-C4烷基; C3-C4烯基; C3-C4炔基; C3-C6环烷基; 酯基; 可选地取代的碳环或杂环基团; 或者R9和R10与它们所连接的氮一起形成一个环,该环可选地被取代; R7表示H或C1-C6烷基; 或者当它们所连接的原子或原子与R6一起形成一个可选地取代的含5,6或7个环原子的单环杂环时; X表示键或式-(Z)n-(Alk)-或-(Alk)-(Z)n-的二价基团,其中Z表示-O-,-S-或-NH-,Alk如在关于R6的定义中所述,n为0或1。
  • Immunomodulating heterocyclic compounds
    申请人:Matthews Richard Ian
    公开号:US20070021428A1
    公开(公告)日:2007-01-25
    Compounds of formula (I) are inhibitors of CD80 and useful in immunomodulation therapy: wherein R 1 and R 3 independently represent H; F; CI; Br; —NO 2 ; —CN; C 1 -C 6 alkyl optionally substituted by F or Cl; or C 1 -C 6 alkoxy optionally substituted by F; R 4 represents a carboxylic acid group (—COOH) or an ester thereof, or —C(═O)NR 6 R 7 , —NR 7 C(═O)R 6 , —NR 7 C(═O)OR 6 , —NHC(═O)NR 7 R 6 or —NHC(═S)NR 7 R 6 wherein R 6 represents H, or a radical of formula -(Alk) m -Q wherein m is 0 or 1, Alk is an optionally substituted divalent straight or branched C 1 -C 12 alkylene, or C 2 -C 12 alkenylene, or C 2 -C 12 alkynylene radical or a divalent C 3 -C 12 carbocyclic radical, any of which radicals may contain one or more —O—, —S— or —N(R 8 )— links wherein R 8 , represents H or C 1 -C 4 alkyl, C 3 -C 4 alkenyl, C 3 -C 4 alkynyl, or C 3 -C 6 cycloalkyl, and Q represents H; —NR 9 R 10 wherein R 9 and R 10 independently represents H; C 1 -C 4 alkyl; C 3 -C 4 alkenyl; C 3 -C 4 alkynyl; C 3 -C 6 cycloalkyl; an ester group; an optionally substituted carbocyclic or heterocyclic group; or R 9 and R 10 form a ring when taken together with the nitrogen to which they are attached, which ring is optionally substituted; and R 7 represents H or C 1 -C 6 alkyl; or when taken together with the atom or atoms to which they are attached R 6 and R 7 form an optionally substituted monocyclic heterocyclic ring having 5, 6 or 7 ring atoms; and X represents a bond or a divalent radical of formula —(Z) n -(Alk)- or -(Alk)-(Z) n — wherein Z represents —O—, —S— or —NH—, Alk is as defined in relation to R 6 , and n is 0 or 1.
    式(I)的化合物是CD80的抑制剂,并且在免疫调节治疗中有用:其中R1和R3分别表示H; F; CI; Br; -NO2; -CN; C1-C6烷基,可选地被F或Cl取代; 或C1-C6烷氧基,可选地被F取代; R4表示羧酸基(-COOH)或其酯,或-C(=O)NR6R7,-NR7C(=O)R6,-NR7C(=O)OR6,-NHC(=O)NR7R6或-NHC(=S)NR7R6,其中R6表示H,或式-(Alk)m-Q的基团,其中m为0或1,Alk为可选取代的二价直链或支链C1-C12烷基,或C2-C12烯基,或C2-C12炔基基团或二价C3-C12环烷基基团,其中任何基团均可能含有一个或多个-O-,-S-或-N(R8)-链接,其中R8表示H或C1-C4烷基,C3-C4烯基,C3-C4炔基或C3-C6环烷基,Q表示H; -NR9R10,其中R9和R10独立地表示H; C1-C4烷基; C3-C4烯基; C3-C4炔基; C3-C6环烷基; 酯基; 可选取代的环烷基或杂环基; 或者当R9和R10与它们所连接的氮一起形成一个环时,该环是可选取代的; R7表示H或C1-C6烷基; 或者当它们所连接的原子或原子与R6和R7一起形成一个可选取代的有5、6或7个环原子的单环杂环时; X表示键或式-(Z)n-(Alk)-或-(Alk)-(Z)n-的二价基团,其中Z表示-O-,-S-或-NH-,Alk如在R6中所定义,n为0或1。
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