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1-[3-[Methyl(2-prop-2-enoyloxyethyl)amino]propanoyloxy]ethenyl 2-methylprop-2-enoate

中文名称
——
中文别名
——
英文名称
1-[3-[Methyl(2-prop-2-enoyloxyethyl)amino]propanoyloxy]ethenyl 2-methylprop-2-enoate
英文别名
1-[3-[methyl(2-prop-2-enoyloxyethyl)amino]propanoyloxy]ethenyl 2-methylprop-2-enoate
1-[3-[Methyl(2-prop-2-enoyloxyethyl)amino]propanoyloxy]ethenyl 2-methylprop-2-enoate化学式
CAS
——
化学式
C15H21NO6
mdl
——
分子量
311.33
InChiKey
JICWIYVIXTWMAD-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):
    2
  • 重原子数:
    22
  • 可旋转键数:
    13
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    82.1
  • 氢给体数:
    0
  • 氢受体数:
    7

文献信息

  • HYDROLYSABLE AND POLYMERIZABLE SILANES WITH ADJUSTABLE SPATIAL DISTRIBUTION OF THE FUNCTIONAL GROUPS, AND USE THEREOF
    申请人:Frauhofer-Gesellschaft zur Foerderung der angewardten forschung e.V.
    公开号:US20140221521A1
    公开(公告)日:2014-08-07
    The present invention relates to a process for a chain extension of radicals bonded to silicon via carbon in silanes or siloxanes while maintaining or increasing the number of functional groups on the respective Si—C-bonded radicals, wherein a silane or siloxane with a radical bonded to a silicon atom by a carbon atom, which bears at least two functional groups, wherein a first group of the functional groups is an unsaturated, organically polymerizable group and a second group of the functional groups is selected from among (a) additional unsaturated, organically polymerizable groups, (b) COOR 8 or —(O) b P(O)(R 5 ) 2 and (c) —OH, with R 8 equal to R 4 or M 1/x x+ wherein M x+ is a hydrogen or an x-fold positively charged metal cation, and b=0 or 1, is converted in a first reaction with a compound of a formula (I) X—W—(Z) a (I) wherein X is SH, NH 2 or NHR 4 , Z is OH, the carboxylic acid radical —COOH or a salt or an ester of this radical or a silyl radical, W is a substituted or non-substituted hydrocarbon, the chain of which can be interrupted by —S—, —O—, —NH—, —NR 4 —, —C(O)O—, —NHC(O)—, —C(O)NH—, —NHC(O)O—, —C(O)NHC(O)—, —NHC(O)NH—, —S(O)—, —C(S)O—, —C(S)NH—, —NHC(S)—, —NHC(S)O—, and a is 1, 2, 3, 4 or a greater whole number, wherein R 4 is a non-substituted or substituted hydrocarbon radical, R 5 is a non-substituted or substituted hydrocarbon radical or OR 6 , R 6 is hydrogen or a non-substituted or substituted hydrocarbon radical to such an extent that the radical X connects to the first functional group. Furthermore, the invention relates to multiple processes, which, based on the aforementioned first reaction, comprise additional process steps and either lead to compounds/silicic acid polycondensates with reactive groups Q, wherein Q is OH, NR 7 2 , NR 7 3 + , CO 2 H, SO 3 H, PO(OH) 2 PO(OR 4 ) 2 or a salt of the aforementioned acids, wherein R 4 has the meaning specified above for formula (I), and R 7 either has the same meaning as R 4 or two radicals R 7 together can represent a potentially substituted, potentially unsaturated alkylene group, or to compounds/silicic acid polycondensates, in which unsaturated, organically polymerizable groups are located farther out, wherein the Si—C-bonded radicals can potentially have a dendrimer-like structure. Products of the process pursuant to the invention and organic polymers produced as a result are likewise encompassed by the invention.
  • US9206205B2
    申请人:——
    公开号:US9206205B2
    公开(公告)日:2015-12-08
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同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸 麦撒奎 鹅膏氨酸 鹅膏氨酸 鸦胆子酸A甲酯 鸦胆子酸A 鸟氨酸缩合物