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3-(Boc-氨基)-3-(4-甲氧基苯基)丙酸 | 96363-20-1

中文名称
3-(Boc-氨基)-3-(4-甲氧基苯基)丙酸
中文别名
3-NBOC-氨基-3-(4-甲氧基苯基)丙酸;3-N-叔丁氧羰基氨基-3-(4-甲氧基苯基)丙酸
英文名称
D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoic acid
英文别名
3-((tert-butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoic acid;D,L-3-{[(1,1-dimethylethoxy)carbonyl]amino}-3-(4-methoxyphenyl)propanoic acid;3-[(Tert-butoxycarbonyl)amino]-3-(4-methoxyphenyl)propanoic acid;3-(4-methoxyphenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
3-(Boc-氨基)-3-(4-甲氧基苯基)丙酸化学式
CAS
96363-20-1
化学式
C15H21NO5
mdl
——
分子量
295.335
InChiKey
OPAAZWPTEYZZIW-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

  • 熔点:
    167-169°C (dec.)
  • 沸点:
    437.02°C (rough estimate)
  • 密度:
    1.1454 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    21
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    84.9
  • 氢给体数:
    2
  • 氢受体数:
    5

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi
  • 安全说明:
    S26,S37/39
  • 危险类别码:
    R36/37/38
  • 海关编码:
    2922509090
  • 危险性防范说明:
    P261,P280,P301+P312,P302+P352,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

SDS

SDS:701c4f2dcbcf33a66f4c581628bc3f25
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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

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文献信息

  • LYSOBACTIN AMIDES
    申请人:VON NUSSBAUM Franz
    公开号:US20090203582A1
    公开(公告)日:2009-08-13
    The invention relates to lysobactin amides and methods for their preparation, as well as their use for manufacturing medicaments for the treatment and/or prophylaxis of diseases, in particular bacterial infectious diseases.
    这项发明涉及赖酸胞素酰胺及其制备方法,以及它们用于制造治疗和/或预防疾病,特别是细菌感染性疾病的药物的用途。
  • A General Synthetic Route to Isomeric Pyrrolo[1,2-<i>x</i>][1,4]diazepinones
    作者:Elena Y. Zelina、Tatyana A. Nevolina、Ludmila N. Sorotskaja、Dmitry A. Skvortsov、Igor V. Trushkov、Maxim G. Uchuskin
    DOI:10.1021/acs.joc.8b01669
    日期:2018.10.5
    A simple one-pot method for the synthesis of isomeric pyrrolo[1,2-x][1,4]diazepinones in reasonable yields was developed. The method is based on the condensation of readily available N-Boc amino acids with biomass-derived furans containing aminoalkyl groups followed by deprotection, furan ring opening, and Paal–Knorr cyclization. Using this approach, we synthesized pyrrolo[1,2-a][1,4]diazepin-3(2H)-ones
    开发了一种简单的一锅法,以合理的产率合成吡咯并[1,2- x ] [1,4]二氮杂ze酮。该方法基于容易获得的N- Boc氨基酸生物质衍生的含基烷基的呋喃的缩合,然后进行脱保护,呋喃开环和Paal-Knorr环化。使用这种方法,我们从糠胺和β-氨基酸吡咯并[1,2- d ] [1,4]二氮杂合成了吡咯并[1,2- a ] [1,4]二氮杂-3(2 H)-来自2-(2-呋喃基)乙胺α-氨基酸的-4(5 H)-1。研究了合成的吡咯并二氮杂酮的细胞毒性。
  • Novel compounds for treatment of cancer and disorders associated with angiogenesis function
    申请人:Neamati Nouri
    公开号:US20060142294A1
    公开(公告)日:2006-06-29
    Novel compounds for treatment of cancer and disorders associated with angiogenesis function. Also disclosed are a method of preparing the compounds, pharmaceutical compositions and packaged products containing the compounds, a method of using these molecules to treat cancer (e.g., leukemia, non-small cell lung cancer, colon cancer, CNS cancer, melanoma, ovarian cancer, breast cancer, renal cancer, and prostate cancer) and disorders associated with angiogenesis function (e.g., age-related macular degeneration, macular dystrophy, and diabetes), a method of monitoring the treatment, a method of profiling gene expression, and a method of modulating gene expression.
    用于治疗癌症和与血管生成功能相关疾病的新化合物。还公开了一种制备这些化合物的方法,包括含有这些化合物的药物组合物和包装产品,一种使用这些分子治疗癌症(例如白血病、非小细胞肺癌、结肠癌、中枢神经系统癌症、黑色素瘤、卵巢癌、乳腺癌、肾癌和前列腺癌)和与血管生成功能相关疾病(例如年龄相关性黄斑变性、黄斑营养不良和糖尿病)的方法,一种监测治疗效果的方法,一种基因表达分析的方法,以及一种调控基因表达的方法。
  • Probes, systems, and methods for drug discovery
    申请人:——
    公开号:US20030125315A1
    公开(公告)日:2003-07-03
    Aspects of the present invention include probes, methods, systems that have stand alone utility and may comprise features of a drug discovery system or method. The present invention also includes pharmaceutical compositions. In more detail, the present invention provides molecular probes and methods for producing molecular probes. The present invention provides also provides systems and methods for new drug discovery. An embodiment of the present invention utilizes sets of probes of the present invention and a new approach to computational chemistry in a drug discovery method having increased focus in comparison to heretofore utilized combinatorial chemistry. The present invention also provides computer software and hardware tools useful in drug discovery systems. In an embodiment of a drug discovery method of the present invention in silico methods and in biologico screening methods are both utilized to maximize the probability of success while minimizing the time and number of wet laboratory steps necessary to achieve the success.
    本发明的方面包括探针、方法、系统,具有独立实用性并可能包括药物发现系统或方法的特征。本发明还包括制药组合物。更详细地说,本发明提供了分子探针和制备分子探针的方法。本发明还提供了新药物发现的系统和方法。本发明的实施例利用本发明的探针集和一种新的计算化学方法在药物发现方法中具有更高的聚焦度,相比之前使用的组合化学方法。本发明还提供了在药物发现系统中有用的计算机软件和硬件工具。在本发明的药物发现方法的实施例中,同时利用了基于计算机的方法和生物筛选方法,以最大化成功的可能性,同时最小化必要的湿实验步骤的时间和数量。
  • NOVEL COMPOUNDS FOR TREATMENT OF CANCER AND DISORDERS ASSOCIATED WITH ANGIOGENESIS FUNCTION
    申请人:Neamati Nouri
    公开号:US20090093489A1
    公开(公告)日:2009-04-09
    Novel compounds for treatment of cancer and disorders associated with angiogenesis function. Also disclosed are a method of preparing the compounds, pharmaceutical compositions and packaged products containing the compounds, a method of using these molecules to treat cancer (e.g., leukemia, non-small cell lung cancer, colon cancer, CNS cancer, melanoma, ovarian cancer, breast cancer, renal cancer, and prostate cancer) and disorders associated with angiogenesis function (e.g., age-related macular degeneration, macular dystrophy, and diabetes), a method of monitoring the treatment, a method of profiling gene expression, and a method of modulating cell growth, cell cycle, apoptosis, or gene expression.
    新型化合物用于治疗癌症和与血管生成功能相关的疾病。还公开了制备这些化合物的方法、含有这些化合物的药物组合物和包装产品、使用这些分子治疗癌症(例如白血病、非小细胞肺癌、结肠癌、中枢神经系统癌症、黑色素瘤、卵巢癌、乳腺癌、肾癌和前列腺癌)和与血管生成功能相关的疾病(例如年龄相关性黄斑变性、黄斑营养不良和糖尿病)的方法、监测治疗的方法、基因表达谱分析的方法以及调节细胞生长、细胞周期、细胞凋亡或基因表达的方法。
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