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3-(3-(benzyloxy)-4-methoxyphenyl)propanal

中文名称
——
中文别名
——
英文名称
3-(3-(benzyloxy)-4-methoxyphenyl)propanal
英文别名
3-(3-(benzyloxy)-4-methoxyphenyl)propionaldehyde;3-(3-Benzyloxy-4-methoxyphenyl)propanal;3-(4-methoxy-3-phenylmethoxyphenyl)propanal
3-(3-(benzyloxy)-4-methoxyphenyl)propanal化学式
CAS
——
化学式
C17H18O3
mdl
——
分子量
270.328
InChiKey
ZQMUDGNASAYKKO-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):
    2.8
  • 重原子数:
    20
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 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:
    参考文献:
    名称:
    The Garuganin and Garugamblin Diarylether Heptanoids: Total Synthesis and Determination of Chiral Properties Using Dynamic NMR
    摘要:
    The synthesis of the garuganin and garugamblin diarylether heptanoids using an intramolecular Ullmann coupling is reported. Alkene stereoisomers, vinylogous ester regioisomers, and beta-diketone congeners are also synthesized. The chiral properties and free energies of activation for racemization of the garuganin and garugamblin diarylether heptanoids and congeners are determined using dynamic NMR methods. A combination of techniques including coalescence measurements, line shape analysis, and selective inversion experiments are used to measure racemization barriers. None of the garuganin or garugamblin diarylether heptanoids are chiral, despite their reported specific rotation values.
    DOI:
    10.1021/jo400157d
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文献信息

  • Process for production of aspartyl dipeptide ester derivative, novel production intermediate therefor, and process for production thereof
    申请人:AJINOMOTO CO. INC
    公开号:US20020133037A1
    公开(公告)日:2002-09-19
    The present invention relates to a method of manufacturing aspartyl dipeptide ester compounds, which can be used as sweeteners, and aldehydes that can be used in the manufacturing processes.
    本发明涉及一种制造天冬氨酰二肽酯化合物的方法,该方法可用作甜味剂,并且还涉及可以在制造过程中使用的醛。
  • 毛兰素类似物及其合成方法和应用
    申请人:中国科学院成都生物研究所
    公开号:CN116535304A
    公开(公告)日:2023-08-04
    本发明属于化合物合成领域,具体涉及毛兰素类似物及其合成方法和应用。具体技术方案为:一类毛兰素类似物,通过特定的连接子链接两个不同的芳香环、多氢芳环或芳香杂环片段形成的化合物,或其构象异构体、旋光异构体或其盐:所述毛兰素类似物为盐时,为所述结构式与矿物酸或有机酸形成的盐。本发明构建这类新的毛兰素类似物的制备方法操作简单、产率高。新构建的毛兰素类似物具有良好的抗癌活性,且半衰期最长为毛兰素的12余倍,具有良好的制药潜力。
  • NOVEL ASPARTYL DIPEPTIDE ESTER DERIVATIVES AND SWEETENERS
    申请人:Ajinomoto Co., Inc.
    公开号:EP1088829A1
    公开(公告)日:2001-04-04
    There are provided novel aspartyl dipeptide ester derivatives (including salts thereof) such as N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-(α-methyl)phenylalanine 1-methyl ester which are usable as sweeteners, and sweeteners, foods and the like containing the same. These derivatives are usable as low-calory sweeteners especially excellent in the degree of sweetness in comparison with the conventional products.
    本文提供了新型天冬氨酰二肽酯衍生物(包括其盐),如 N-[N-[3-(3-羟基-4-甲氧基苯基)丙基]-L-α-天冬氨酰]-L-(α-甲基)苯丙氨酸 1-甲酯,可用作甜味剂,以及含有这些衍生物的甜味剂、食品等。 这些衍生物可用作低热量甜味剂,与传统产品相比,其甜度尤其出色。
  • PROCESS FOR THE PRODUCTION OF ASPARTYLDIPEPTIDE ESTER DERIVATIVES, NOVEL INTERMEDIATES THEREFOR AND PROCESS FOR THE PRODUCTION OF THE INTERMEDIATES
    申请人:Ajinomoto Co., Inc.
    公开号:EP1231215A1
    公开(公告)日:2002-08-14
    In the present invention, efficient and industrial processes for production of aspartyl dipeptide ester derivative represented by the general formula (3) expected to serve as a sweetener, and aldehydes represented by the general formulae (1) and (2) which are intermediates therefor are provided. Among them, a process for producing industrially and efficiently N-[N-[3-(3-hydroxy-4-methoxyphenyl) propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester particularly excellent as a sweetener having a high sweetening potency, a development of intermediate for the production particularly useful and advantageous therefor, and an efficient process for production thereof are provided.
    在本发明中,提供了生产通式(3)所代表的有望用作甜味剂的天冬氨酰二肽酯衍生物以及作为其中间体的通式(1)和(2)所代表的醛的高效工业工艺。 其中,提供了一种工业化高效生产 N-[N-[3-(3-羟基-4-甲氧基苯基)丙基]-L-α-天冬氨酰]-L-苯丙氨酸 1-甲酯的工艺,该工艺作为甜味剂特别出色,具有很高的增甜效力,还提供了一种对其特别有用和有利的生产中间体的开发及其高效生产工艺。
  • US6630191B1
    申请人:——
    公开号:US6630191B1
    公开(公告)日:2003-10-07
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