摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N-adamantan-1-yl acrylamide | 105077-42-7

中文名称
——
中文别名
——
英文名称
N-adamantan-1-yl acrylamide
英文别名
N-(adamantan-2-yl)prop-2-enamide;N-(2-adamantyl)prop-2-enamide
N-adamantan-1-yl acrylamide化学式
CAS
105077-42-7
化学式
C13H19NO
mdl
——
分子量
205.3
InChiKey
XPRPLYWRNZUUHW-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:
    376.1±15.0 °C(Predicted)
  • 密度:
    1.08±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.77
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    三乙胺2,6-二叔丁基-4-巯基苯酚N-adamantan-1-yl acrylamide三乙胺 、 silica 、 Ethyl acetate ether hexane 作用下, 以 甲醇 为溶剂, 反应 12.0h, 生成 3-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]thio]-N-tricyclo[3.3.1.13,7]dec-2-yl propanamide
    参考文献:
    名称:
    Bicycloalkyl tricycloalkyl, azabicycloalkyl and azatricycoalkyl amides
    摘要:
    本发明的化合物是由以下式子表示的双环、三环、氮杂双环和氮杂三环酰胺:##STR1## 其中:R.sub.1和R.sub.2是以下组成的同类或异类成员:卤素、苯基、取代苯基和一个##STR2##组,其中n、m和p独立地是1至8的整数,但n+m+p小于或等于10;X是硫、亚砜或磺酰基;Alk是直链或支链低碳链;R.sub.3选自以下组成的群体:双环烷基氨基、三环烷基氨基、氮杂双环烷基、氮杂三环烷基、氮杂双环烷基氨基、氮杂三环烷基氨基或二环烷基氨基。这些化合物可用作抗炎和抗过敏剂。
    公开号:
    US05019597A1
  • 作为产物:
    描述:
    2-氨基金刚烷丙烯酰氯三乙胺 作用下, 以 四氢呋喃 为溶剂, 以75%的产率得到N-adamantan-1-yl acrylamide
    参考文献:
    名称:
    Highly Elastic Supramolecular Hydrogels Using Host–Guest Inclusion Complexes with Cyclodextrins
    摘要:
    Supramolecular hydrogels, which are cross-linked via host guest interactions, show high-performance physical properties, such as elasticity and toughness. Herein we prepare a supramolecular hydrogel without chemical crosslinker. The supramolecular hydrogel was prepared by polymerization of the inclusion complexes between beta-cyclodextrin acrylamide and adamantane acrylamide monomers. The beta-cyclodextrin adamantane gel (beta CD Ad gel) shows a high stretching property (990%). The initial strain (0%) is restored in several minutes for a beta CD Ad gel stretched to 180% of the initial strain without altering the physical history. However, chemically cross-linked poly(acrylamide) does not show the reversible stretching property. These results indicate that host guest interaction inside the supramolecular hydrogel plays an important role in the shape recovery properties.
    DOI:
    10.1021/ma400695p
点击查看最新优质反应信息

文献信息

  • Bicycloalky, tricycloalkyl, azabicycloalkyl, and azatricycloalkyl thio
    申请人:G. D. Searle & Co.
    公开号:US05157053A1
    公开(公告)日:1992-10-20
    The compounds of this invention are bicyclic, tricyclic, azabicyclic and azatricyclic amides represented by the formula: ##STR1## wherein: R.sub.1 and R.sub.2 are the same or different members of the group consisting of halo, phenyl, substituted phenyl and a ##STR2## group wherein n, m and p are independently an integer of from 1 to 8 provided that n+m+p is equal to or less than 10; x is thio, sulfinyl or sulfonyl; Alk is straight or branched chain lower alkylene; R.sub.3 is selected from the group-consisting of a bicycloalkylamino, tricycloalkylamino, azabicycloalkyl, azatricycloalkyl, aszabicycloalkylamino, azatricycloalkylamino or dicycloalkylamino, The compounds are useful as anti-inflammatory and anti-allergy agents.
    本发明的化合物是由下式表示的双环、三环、氮杂双环和氮杂三环酰胺:##STR1## 其中:R.sub.1和R.sub.2是卤素、苯基、取代苯基和##STR2##基团中相同或不同的成员,其中n、m和p是独立的1至8的整数,前提是n+m+p等于或小于10;x是硫、亚硫酰或磺酰基;Alk是直链或支链低级烷基;R.sub.3选自以下群体:双环烷基氨基、三环烷基氨基、氮杂双环烷基、氮杂三环烷基、aszabicycloalkylamino、azatricycloalkylamino或二环烷基氨基。这些化合物可用作抗炎和抗过敏剂。
  • Azabicycloalkyl and azatricycloalkyl amides
    申请人:G. D. Searle & Co.
    公开号:US05198435A1
    公开(公告)日:1993-03-30
    The compounds of this invention are bicyclic, tricyclic, azabicyclic and azatricyclic amides represented by the formula: ##STR1## wherein: R.sub.1 and R.sub.2 are the same or different members of the group consisting of halo, phenyl, substituted phenyl and a ##STR2## group wherein n, m and p are independently an integer of from 1 to 8 provided than n+m+p is equal to or less than 10; x is thio, sulfinyl or sulfonyl; Alk is straight or branched chain lower alkylene; R.sub.3 is selected from the group consisting of a bicycloalkylamino, tricycloalkylamino, azabicycloalkyl, azatricycloalkyl, azabicycloalkylamino, azatricycloalkylamino or dicycloalkylamino. The compounds are useful as anti-inflammatory and anti-allergy agents.
    本发明的化合物是由下式表示的双环、三环、氮杂双环和氮杂三环酰胺:##STR1## 其中:R.sub.1和R.sub.2是卤素、苯基、取代苯基和一个##STR2##基团的相同或不同成员,其中n、m和p是独立的1到8的整数,前提是n+m+p等于或小于10;x是硫、亚砜或磺酰基;Alk是直链或支链低碳链;R.sub.3选自自行车烷基氨基、三自行车烷基氨基、氮杂自行车烷基、氮杂三环烷基、氮杂自行车烷基氨基、氮杂三环烷基氨基或二自行车烷基氨基的群。这些化合物可用作抗炎和抗过敏剂。
  • Bicycloalkyl tricycloalkyl, azabicycloalkyl and azatricycoalkyl amides
    申请人:G. D. Searle & Co.
    公开号:US05019597A1
    公开(公告)日:1991-05-28
    The compounds of this invention are bicyclic, tricyclic, azabicyclic and azatricyclic amides represented by the formula: ##STR1## wherein: R.sub.1 and R.sub.2 are the same or different members of the group consisting of halo, phenyl, substituted phenyl and a ##STR2## group wherein n, m and p are independently an integer of from 1 to 8 provided that n+m+p is equal to or less than 10; X is thio, sulfinyl or sulfonyl; Alk is straight or branched chain lower alkylene; R.sub.3 is selected from the group consisting of a bicycloalkylamino, tricycloalkylamino, azabicycloalkyl, azatricycloalkyl, azabicycloalkylamino, azatricycloalkylamino or dicycloalkylamino. The compounds are useful as anti-inflammatory and anti-allergy agents.
    本发明的化合物是由以下式子表示的双环、三环、氮杂双环和氮杂三环酰胺:##STR1## 其中:R.sub.1和R.sub.2是以下组成的同类或异类成员:卤素、苯基、取代苯基和一个##STR2##组,其中n、m和p独立地是1至8的整数,但n+m+p小于或等于10;X是硫、亚砜或磺酰基;Alk是直链或支链低碳链;R.sub.3选自以下组成的群体:双环烷基氨基、三环烷基氨基、氮杂双环烷基、氮杂三环烷基、氮杂双环烷基氨基、氮杂三环烷基氨基或二环烷基氨基。这些化合物可用作抗炎和抗过敏剂。
  • Bicycloalkyl, tricycloalkyl, azabicycloalkyl and azatricycloalkyl amides
    申请人:G.D. Searle & Co.
    公开号:EP0190684A2
    公开(公告)日:1986-08-13
    The compounds of this invention are bicyclic, tricyclic, azabicyclic and azatricyclic amides represented by the formula: wherein: R, and R2 are the same or different members of the group consisting of halo, phenyl, substituted phenyl and a group wherein n, m and p are independently an integer of from 1 to 8 provided that n + m + p is equal to or less than 10; X is thio, sulfinyl or sulfonyl; Alk is straight or branched chain lower alkylene; R3 is selected from the group consisting of a bicycloalkylamino, tricycloalkylamino, azabicycloalkyl, azatricycloalkyl, azabicycloalkylamino, azatricycloalkylamino or dicycloalkylamino. The compounds are useful as anti-inflammatory and anti-allergy agents.
    本发明的化合物为双环、三环、氮杂双环和氮杂环酰胺,由式表示: 其中R、和 R2 是卤代、苯基、取代苯基和一个基团组成的组中相同或不同的成员 其中 n、m 和 p 独立地为 1 至 8 的整数,条件是 n + m + p 等于或小于 10;X 为硫代、亚磺酰基或磺酰基;Alk 为直链或支链低级亚烷基;R3 选自由双环烷基氨基、三环烷基氨基、氮杂环烷基、氮杂环烷基、氮杂环烷基氨基、氮杂环烷基氨基或二环烷基氨基组成的组。这些化合物可用作抗炎剂和抗过敏剂。
  • Process for producing aqueous ink for inkjet printing
    申请人:KAO CORPORATION
    公开号:EP0857766A1
    公开(公告)日:1998-08-12
    A process for producing an aqueous ink for inkjet printing capable of giving an elevated print density of printed matters, being improved in fixability to the material to be printed, water resistance and improved storage stability and scarcely scorching onto a printer head. This process comprises dissolving a salt-forming group-having polymer and a hydrophobic dye in a water-insoluble organic solvent to obtain a solution, adding water and a neutralizing agent optionally together with a surfactant to the solution to ionize the salt-forming group of the polymer, emulsifying the resulting mixture, and removing out the solvent from the emulsion to obtain an ink containing an aqueous dispersion of the polymer particles in which the dye has been encompassed.
    一种用于喷墨打印的水性墨水的生产工艺,这种墨水能够提高打印物的打印密度,改善对打印材料的固定性、耐水性和贮存稳定性,并且在打印头上几乎不会焦化。该工艺包括:将含盐基团的聚合物和疏水性染料溶解在不溶于水的有机溶剂中,得到溶液;向溶液中加入水和中和剂(可选择与表面活性剂一起加入),使聚合物的含盐基团电离;乳化得到的混合物;从乳液中除去溶剂,得到含有聚合物颗粒水性分散体的墨水,染料已被包在其中。
查看更多

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