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

carbamic acid-(1-methyl-but-3-ynyl ester) | 89598-51-6

中文名称
——
中文别名
——
英文名称
carbamic acid-(1-methyl-but-3-ynyl ester)
英文别名
Carbamidsaeure-(1-methyl-but-3-inylester);4-Carbamoyloxy-pent-1-in;Pent-4-yn-2-yl carbamate
carbamic acid-(1-methyl-but-3-ynyl ester)化学式
CAS
89598-51-6
化学式
C6H9NO2
mdl
MFCD19209089
分子量
127.143
InChiKey
DJSPNARHFUZDJE-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):
    0.6
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    52.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    参考文献:
    名称:
    The Prevalence of Daytime Napping and Its Relationship to Nighttime Sleep
    摘要:
    Many healthy adults report daytime napping. Surprisingly few studies, however have examined spontaneous napping behavior especially very short naps, in healthy adults. The authors examined the prevalence of power naps (lasting less than 20 minutes) and longer naps (20 minutes or more) and their effects on nighttime sleep in a group of healthy young and middle-aged adults. The young and middle-aged adults reported very similar sleep and napping patterns, with approximately 74% of the participants in both groups reporting they had napped during a 7-day sleep-log period. Almost half of the participants reported that the average nap lasted less than 20 minutes. A multivariant analysis of variance (MANOVA) found no significant differences between the no-nap and the power-nap or long-nap groups in sleep quantity or quality for either age group. The current data suggested that power napping occurs frequently in healthy adults and that spontaneous napping does not negatively affect nighttime sleep.
    DOI:
    10.1080/08964280109595773
点击查看最新优质反应信息

文献信息

  • [EN] FUNGICIDAL 3-{PHENYL[(HETEROCYCLYLMETHOXY)IMINO]METHYL}-HETEROCYCLE DERIVATIVES<br/>[FR] DÉRIVÉS 3-{PHENYL[(HETEROCYCLYLMETHOXY)IMINO]METHYL}-HETEROCYCLE FONGICIDES
    申请人:BAYER CROPSCIENCE AG
    公开号:WO2014135608A1
    公开(公告)日:2014-09-12
    The present invention provides 3-phenyl[(heterocyclylmethoxy)imino]methyl}-heterocyclyl derivatives of formula (I) Wherein A, X1 to X3, Y1 to Y5 represent various substituents.
    本发明提供了公式(I)的3-苯基[(杂环基甲氧基)亚胺]甲基}-杂环基衍生物,其中A、X1至X3、Y1至Y5代表各种取代基。
  • [EN] FUNGICIDAL 3-[(PYRIDIN-2-YLMETHOXYIMINO)(PHENYL)METHYL]-2-SUBSTITUTED-1,2,4-OXADIAZOL-5(2H)-ONE DERIVATIVES<br/>[FR] DÉRIVÉS FONGICIDES DE 3-[(PYRIDIN-2-YLMÉTHOXYIMINO)(PHÉNYL)MÉTHYL]-2-SUBSTITUÉ-1,2,4-OXADIAZOL-5(2H)-ONE
    申请人:BAYER IP GMBH
    公开号:WO2013098147A1
    公开(公告)日:2013-07-04
    The present invention relates to 3-[(pyridin-2-ylmethoxyimino)(phenyl)methyl]-2-substituted-1,2,4-oxadiazol-5(2H)-one derivatives of formula (I), their process of preparation, their use as fungicide active agents, particularly in the form of fungicide compositions, and methods for the control of phytopathogenic fungi, notably of plants, using these compounds or compositions.
    本发明涉及式(I)的3-[(吡啶-2-基甲氧基亚胺)(苯基)甲基]-2-取代-1,2,4-噁二唑-5(2H)-酮衍生物,其制备方法,它们作为杀真菌活性剂的用途,特别是作为杀真菌组合物的形式,以及利用这些化合物或组合物控制植物病原真菌,尤其是植物的方法。
  • [EN] ACYLPHOSPHINE OXIDE PHOTOINITIATORS<br/>[FR] PHOTO-INITIATEURS À BASE D'OXYDE D'ACYLPHOSPHINE
    申请人:AGFA GRAPHICS NV
    公开号:WO2017191043A1
    公开(公告)日:2017-11-09
    Thiol modified acylphosphine oxide photoinitiators exhibiting improved smell and extractability are disclosed. Also disclosed is a UV curable inkjet ink containing an acylphosphine oxide photoinitiator and a polymerizable compound, wherein the acylphosphine oxide photoinitiator includes one or more acyl groups substituted by a thiol.
    揭示了改善气味和可提取性的醇改性酰基膦氧化物光引发剂。还揭示了一种含有酰基膦氧化物光引发剂和可聚合化合物的紫外固化喷墨墨,其中酰基膦氧化物光引发剂包括一个或多个由醇取代的酰基。
  • FUNGICIDAL 3-[(1,3-THIAZOL-4-YLMETHOXYIMINO)(PHENYL)METHYL]-2-SUBSTITUTED-1,2,4-OXADIAZOL-5(2H)-ONE DERIVATIVES
    申请人:BAYER INTELLECTUAL PROPERTY GMBH
    公开号:US20150031730A1
    公开(公告)日:2015-01-29
    The present invention relates to 3-[(1,3-thiazol-4-ylmethoxyimino)(phenyl)methyl]-2-substituted-1,2,4-oxadiazol-5(2H)-one derivatives of formula (I), their process of preparation, their use as fungicide active agents, particularly in the form of fungicide compositions, and methods for the control of phytopathogenic fungi, notably of plants, using these compounds or compositions.
    本发明涉及式(I)的3-[(1,3-噻唑-4-基甲氧基亚胺)(苯基)甲基]-2-取代-1,2,4-噁二唑-5(2H)-酮衍生物的制备方法,它们作为杀真菌活性剂的用途,特别是以杀真菌组合物的形式,以及使用这些化合物或组合物控制植物病原真菌,尤其是植物的方法。
  • FUNGICIDAL 3-[(PYRIDIN-2-YLMETHOXYIMINO)(PHENYL)METHYL]-2-SUBSTITUTED-1,2,4-OXADIAZOL-5(2H)-ONE DERIVATIVES
    申请人:BAYER INTELLECTUAL PROPERTY GMBH
    公开号:US20140350058A1
    公开(公告)日:2014-11-27
    The present invention relates to 3-[(pyridin-2-ylmethoxyimino)(phenyl)methyl]-2-substituted-1,2,4-oxadiazol-5(2H)-one derivatives of formula (I), their process of preparation, their use as fungicide active agents, particularly in the form of fungicide compositions, and methods for the control of phytopathogenic fungi, notably of plants, using these compounds or compositions.
    本发明涉及式(I)的3-[(吡啶-2-基甲氧基亚胺)(苯基)甲基]-2-取代-1,2,4-噁二唑-5(2H)-酮衍生物的制备方法,它们作为杀真菌活性剂的用途,特别是作为杀真菌组合物的形式,以及使用这些化合物或组合物控制植物病原真菌的方法。
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-[[[(1R,2R)-2-[[[3,5-双(叔丁基)-2-羟基苯基]亚甲基]氨基]环己基]硫脲基]-N-苄基-N,3,3-三甲基丁酰胺 (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,4R)-Boc-4-环己基-吡咯烷-2-羧酸 (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-N,3,3-三甲基-N-(苯甲基)丁酰胺 (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)-2-氨基-3,3-二甲基-N-2-吡啶基丁酰胺 (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,5R,6R)-5-(1-乙基丙氧基)-7-氧杂双环[4.1.0]庚-3-烯-3-羧酸乙基酯 (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(1-6) 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