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

6-丙基烟醛 | 143142-34-1

中文名称
6-丙基烟醛
中文别名
——
英文名称
6-propylnicotinaldehyde
英文别名
6-propylpyridine-3-carbaldehyde
6-丙基烟醛化学式
CAS
143142-34-1
化学式
C9H11NO
mdl
MFCD18804180
分子量
149.192
InChiKey
FKWPVUNGBPPVTL-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:
    249.9±20.0 °C(Predicted)
  • 密度:
    1.038±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    30
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:d41d000aba0c77db3afe3ee156cf9089
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    6-丙基烟醛哌啶N,N'-二环己基碳二亚胺 作用下, 以 1,4-二氧六环吡啶 为溶剂, 生成
    参考文献:
    名称:
    Acrylamide derivatives as antiallergic agents. 2. Synthesis and structure activity relationships of N-[4-[4-(diphenylmethyl)-1-piperazinyl]butyl]-3-(3-pyridyl)acrylamides
    摘要:
    A new series of 3-(3-pyridyl)acrylamides 16, 17, 19, and 26, and 5-(3-pyridyl)-2,4-pentadienamides 20-25 were prepared and evaluated for their antiallergic activity. Several of these compounds exhibited more potent inhibitory activities than the parent compound 1a [(E)-N-[4-[4-(diphenylmethyl)-1-piperazinyl]butyl]-3- (3-pyridyl)acrylamide] against the rat passive cutaneous anaphylaxis (PCA) reaction and the enzyme 5-lipoxygenase. Particularly, (E)-N-[4-[4-(diphenylmethyl)-1-piperazinyl]butyl]-3- (6-methyl-3-pyridyl)acrylamide (17p) showed an ED50 value of 3.3 mg/kg po in the rat PCA test, which was one-fifth of ketotifen and oxatomide. As compared with ketotifen and oxatomide, compound 17p (AL-3264) possessed a better balance of antiallergic properties due to inhibition of chemical mediator release, inhibition of 5-lipoxygenase, and antagonism of histamine.
    DOI:
    10.1021/jm00123a012
  • 作为产物:
    描述:
    6-氯烟酸甲酯(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloridepotassium phosphate 、 palladium on activated charcoal 、 氢气异丙基氯化镁二异丁基氢化铝 作用下, 以 四氢呋喃1,4-二氧六环甲醇甲苯 为溶剂, -78.0~80.0 ℃ 、137.9 kPa 条件下, 反应 16.5h, 生成 6-丙基烟醛
    参考文献:
    名称:
    ISOQUINOLINE DERIVATIVES AS MGAT2 INHIBITORS
    摘要:
    Formula I的化合物作为MGAT2抑制剂,可用于预防、治疗或作为高脂血症、糖尿病和肥胖的治疗药物。
    公开号:
    US20180009796A1
点击查看最新优质反应信息

文献信息

  • [EN] PYRIDO (4,3-B) INDOLES CONTAINING RIGID MOIETIES<br/>[FR] PYRIDO[4,3-B]INDOLES CONTENANT DES FRAGMENTS RIGIDES
    申请人:MEDIVATION TECHNOLOGIES INC
    公开号:WO2010051501A1
    公开(公告)日:2010-05-06
    This disclosure is directed to pyrido[4,3-b]indoles having rigid moieties. The compounds in one embodiment are pyrido[4,3-b]indoles having an unsaturated hydrocarbon moiety. The compounds in another embodiment are pyrido[4,3-b]indoles having a cycloalkyl, cycloalkenyl or heterocyclyl moiety. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本公开涉及具有刚性基团的吡啶并[4,3-b]吲哚化合物。在一个实施例中,这些化合物是具有不饱和碳氢基团的吡啶并[4,3-b]吲哚化合物。在另一个实施例中,这些化合物是具有环烷基、环烯基或杂环基团的吡啶并[4,3-b]吲哚化合物。还提供了包括这些化合物的药物组合物,以及使用这些化合物在各种治疗应用中的方法,包括治疗认知障碍、精神障碍、神经递质介导的障碍和/或神经元障碍。
  • Diastereoselective and Highly Enantioselective Henry Reactions using C1-Symmetrical Copper(II) Complexes
    作者:Antoinette Chougnet、Guoqi Zhang、Kegang Liu、Daniel Häussinger、Andreas Kägi、Thomas Allmendinger、Wolf-D. Woggon
    DOI:10.1002/adsc.201100157
    日期:2011.7
    Catalytic Henry reactions of aliphatic aldehydes and prochiral nitro compounds were investigated using copper(II) complexes of 14 C1‐symmetrical ligands derived from (1R,2R)(−)‐diaminocyclohexane. β‐Nitro alcohols with syn:anti ratios of up to 5.7 and excellent ee values for both diastereosimers were obtained.
    使用衍生自(1 R,2 R)(-)-二氨基环己烷的14 C 1对称配体的铜(II)配合物研究了脂肪醛和前手性硝基化合物的催化亨利反应。β硝基醇与顺式:反向上的比率5.7和优异的ee值获得两个diastereosimers值。
  • Non-Flushing Niacin Analogues, and Methods of Use Thereof
    申请人:Bachovchin William W.
    公开号:US20090312355A1
    公开(公告)日:2009-12-17
    One aspect of the present invention relates to substituted pyridines and pharmaceutically acceptable salts thereof that are active against a range of mammalian maladies. Another aspect of the invention relates to a pharmaceutical composition, comprising a compound of the present invention or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient. The present invention also relates to methods of treating a range of mammalian maladies or conditions, including but not limited to hyperlipidemia, hypercholesterolemia, atherosclerosis, coronary artery disease, congestive heart failure, cardiovascular disease, hypertension, coronary heart disease, angina, pellagra, Hartnup's syndrome, carcinoid syndrome, arterial occlusive disease, obesity, hypothyroidism, vasoconstriction, osteoarthritis, rheumatoid arthritis, diabetes, Alzheimer's disease, lipodystrophy, or dyslipidemia, raising serum high-density lipoprotein (HDL) levels, and lowering serum low-density lipoprotein (LDL) levels.
    本发明的一个方面涉及取代吡啶及其药学上可接受的盐,对一系列哺乳动物疾病具有活性。本发明的另一个方面涉及一种制药组合物,包括本发明的化合物或其药学上可接受的盐,以及药学上可接受的载体。本发明还涉及治疗一系列哺乳动物疾病或病症的方法,包括但不限于高脂血症、高胆固醇血症、动脉粥样硬化、冠状动脉疾病、充血性心力衰竭、心血管疾病、高血压、冠心病、心绞痛、糙皮病、哈特努普综合征、类癌综合征、动脉闭塞性疾病、肥胖症、甲状腺功能减退症、血管收缩、骨关节炎、类风湿性关节炎、糖尿病、阿尔茨海默病、脂肪萎缩症或血脂异常,提高血清高密度脂蛋白(HDL)水平,降低血清低密度脂蛋白(LDL)水平。
  • PYRIDO[4,3-B]INDOLES CONTAINING RIGID MOIETIES
    申请人:HUNG David T.
    公开号:US20100216814A1
    公开(公告)日:2010-08-26
    This disclosure is directed to pyrido[4,3-b]indoles having rigid moieties. The compounds in one embodiment are pyrido[4,3-b]indoles having an unsaturated hydrocarbon moiety. The compounds in another embodiment are pyrido[4,3-b]indoles having a cycloalkyl, cycloalkenyl or heterocyclyl moiety. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本文揭示了具有刚性基团的吡啶并[4,3-b]吲哚。在一种实施例中,化合物是具有不饱和碳氢基团的吡啶并[4,3-b]吲哚。在另一种实施例中,化合物是具有环烷基,环烯基或杂环基团的吡啶并[4,3-b]吲哚。还提供了包括这些化合物的制药组合物,以及使用这些化合物进行各种治疗应用的方法,包括治疗认知障碍,精神障碍,神经递质介导的障碍和/或神经元障碍。
  • Pyrido[4,3-B]indoles containing rigid moieties
    申请人:Medivation Technologies, Inc.
    公开号:US08906925B2
    公开(公告)日:2014-12-09
    This disclosure is directed to pyrido[4,3-b]indoles having rigid moieties. The compounds in one embodiment are pyrido[4,3-b]indoles having an unsaturated hydrocarbon moiety. The compounds in another embodiment are pyrido[4,3-b]indoles having a cycloalkyl, cycloalkenyl or heterocyclyl moiety. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本公开涉及具有刚性基团的吡啶并[4,3-b]吲哚。在一种实施例中,化合物是具有不饱和碳氢基团的吡啶并[4,3-b]吲哚。在另一种实施例中,化合物是具有环烷基,环烯基或杂环基团的吡啶并[4,3-b]吲哚。还提供了包含该化合物的制药组合物,以及使用该化合物在多种治疗应用中的方法,包括治疗认知障碍,精神疾病,神经递质介导的疾病和/或神经元疾病。
查看更多

同类化合物

(S)-氨氯地平-d4 (R,S)-可替宁N-氧化物-甲基-d3 (R)-N'-亚硝基尼古丁 (5E)-5-[(2,5-二甲基-1-吡啶-3-基-吡咯-3-基)亚甲基]-2-亚磺酰基-1,3-噻唑烷-4-酮 (5-溴-3-吡啶基)[4-(1-吡咯烷基)-1-哌啶基]甲酮 (5-氨基-6-氰基-7-甲基[1,2]噻唑并[4,5-b]吡啶-3-甲酰胺) (2S)-2-[[[9-丙-2-基-6-[(4-吡啶-2-基苯基)甲基氨基]嘌呤-2-基]氨基]丁-1-醇 (2R,2''R)-(+)-[N,N''-双(2-吡啶基甲基)]-2,2''-联吡咯烷四盐酸盐 黄色素-37 麦斯明-D4 麦司明 麝香吡啶 鲁非罗尼 鲁卡他胺 高氯酸N-甲基甲基吡啶正离子 高氯酸,吡啶 高奎宁酸 马来酸溴苯那敏 马来酸左氨氯地平 顺式-双(异硫氰基)(2,2'-联吡啶基-4,4'-二羧基)(4,4'-二-壬基-2'-联吡啶基)钌(II) 顺式-二氯二(4-氯吡啶)铂 顺式-二(2,2'-联吡啶)二氯铬氯化物 顺式-1-(4-甲氧基苄基)-3-羟基-5-(3-吡啶)-2-吡咯烷酮 顺-双(2,2-二吡啶)二氯化钌(II) 水合物 顺-双(2,2'-二吡啶基)二氯化钌(II)二水合物 顺-二氯二(吡啶)铂(II) 顺-二(2,2'-联吡啶)二氯化钌(II)二水合物 非那吡啶 非洛地平杂质C 非洛地平 非戈替尼 非尼拉朵 非尼拉敏 阿雷地平 阿瑞洛莫 阿培利司N-6 阿伐曲波帕杂质40 间硝苯地平 间-硝苯地平 锇二(2,2'-联吡啶)氯化物 链黑霉素 链黑菌素 银杏酮盐酸盐 铬二烟酸盐 铝三烟酸盐 铜-缩氨基硫脲络合物 铜(2+)乙酸酯吡啶(1:2:1) 铁5-甲氧基-6-甲基-1-氧代-2-吡啶酮 钾4-氨基-3,6-二氯-2-吡啶羧酸酯 钯,二氯双(3-氯吡啶-κN)-,(SP-4-1)-