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1-p-Anisyl-1-aminobutan | 51089-97-5

中文名称
——
中文别名
——
英文名称
1-p-Anisyl-1-aminobutan
英文别名
1-(4-methoxy-phenyl)-butylamine;1-(4-methoxyphenyl)butan-1-amine;1-(4-Methoxyphenyl)butylamine
1-p-Anisyl-1-aminobutan化学式
CAS
51089-97-5
化学式
C11H17NO
mdl
——
分子量
179.262
InChiKey
YFIJHKACBGRMFQ-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:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    35.2
  • 氢给体数:
    1
  • 氢受体数:
    2

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

反应信息

  • 作为反应物:
    描述:
    1-p-Anisyl-1-aminobutan 生成 N-[1-(4-methoxy-phenyl)-butyl]-acetamide
    参考文献:
    名称:
    Bringi; Phalnikar; Bhide, Journal of the University of Bombay, Science: Physical Sciences, Mathematics, Biological Sciences and Medicine, 1950, vol. 18/5A, p. 25
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    Bringi; Phalnikar; Bhide, Journal of the University of Bombay, Science: Physical Sciences, Mathematics, Biological Sciences and Medicine, 1950, vol. 18/5A, p. 25
    摘要:
    DOI:
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文献信息

  • Biphenylcarboxylic acid amides, the preparation thereof and the use thereof as medicaments
    申请人:——
    公开号:US20020032238A1
    公开(公告)日:2002-03-14
    The present invention relates to substituted piperazine derivatives of general formula 1 wherein R 1 to R 7 are defined herein, the isomers and salts thereof, particularly the physiologically acceptable salts thereof, which are valuable inhibitors of the microsomal triglyceride-transfer protein (MTP), medicaments containing these compounds and their use, as well as the preparation thereof.
    本发明涉及一般式1的取代哌嗪衍生物,其中R1至R7在此处定义,其异构体和盐,特别是其生理上可接受的盐,这些盐是微粒体三酰甘油转移蛋白(MTP)的有价值的抑制剂,含有这些化合物的药物以及它们的用途,以及其制备。
  • Novel flavors, flavor modifiers, tastants, taste enhancers, umami or sweet tastants, and/or enhancers and use thereof
    申请人:Tachdjian Catherine
    公开号:US20050084506A1
    公开(公告)日:2005-04-21
    The present invention relates to the discovery that certain non-naturally occurring, non-peptide amide compounds and amide derivatives, such as oxalamides, ureas, and acrylamides, are useful flavor or taste modifiers, such as a flavoring or flavoring agents and flavor or taste enhancer, more particularly, savory (the “umami” taste of monosodium glutamate) or sweet taste modifiers,—savory or sweet flavoring agents and savory or sweet flavor enhancers, for food, beverages, and other comestible or orally administered medicinal products or compositions.
    本发明涉及发现,某些非天然存在的非肽酰胺化合物和酰胺衍生物,如草酰胺、脲和丙烯酰胺,可用作风味或口味调节剂,例如风味或调味剂和风味或口味增强剂,更具体地说,是用于食品、饮料和其他可食用或口服药品或组合物的风味或口味调节剂,包括鲜味(味精的“鲜味”)或甜味调节剂,鲜味或甜味调味剂以及鲜味或甜味增强剂。
  • Combination of MTP inhibitors or apoB-secretion inhibitors with fibrates for use as pharmaceuticals
    申请人:Boehringer Ingelheim Pharma KG
    公开号:US20030162788A1
    公开(公告)日:2003-08-28
    The invention relates to the use of fibrates for lowering the liver toxicity of MTP inhibitors as well as pharmaceutical compositions containing an MTP inhibitor and a fibrate.
    本发明涉及使用纤维酸衍生物来降低MTP抑制剂对肝脏的毒性,以及包含MTP抑制剂和纤维酸衍生物的药物组合物。
  • Heteroarylcarboxylic acid amides, the preparation thereof and their use as pharmaceutical compositions
    申请人:Boehringer Ingelheim Pharma KG
    公开号:US20030073836A1
    公开(公告)日:2003-04-17
    A compound of formula 1 wherein: A a , R a , X 1 to X 4 , Het, and R 5 to R 7 are defined as in claim 1, the isomers and the salts thereof, particularly the physiologically acceptable salts thereof, which are valuable inhibitors of the microsomal triglyceride-transfer protein (MTP), medicaments containing these compounds and their use, as well as the preparation thereof.
    根据权利要求1中定义的Aa、Ra、X1至X4、Het和R5至R7,本发明的化合物公式1包括这些化合物的同分异构体和盐,尤其是具有生理活性的盐,它们是微囊体甘油三酯转移蛋白(MTP)的有效抑制剂,含有这些化合物的药物及其用途,以及这些化合物的制备方法。
  • N6-SUBSTITUTED ADENOSINE DERIVATIVES AND N6-SUBSTITUTED ADENINE DERIVATIVES AND USES THEREOF
    申请人:Shi Jiangong
    公开号:US20130045942A1
    公开(公告)日:2013-02-21
    The present invention provides N 6 -substituted adenosine derivatives and N 6 -substituted adenine derivatives, manufacturing methods thereof, a pharmaceutical composition comprising the said compounds above, and uses of these compounds in manufacturing medicaments and health-care products for treating insomnia, convulsion, epilepsy, and Parkinson's diseases, and preventing and treating dementia.
    本发明提供了N6-取代腺苷衍生物和N6-取代腺嘌呤衍生物,其制备方法,包括上述化合物的药物组合物,以及这些化合物在制造治疗失眠、惊厥、癫痫和帕金森病的药物和保健产品以及预防和治疗痴呆症中的用途。
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