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2-氨基-4-乙酰基苯甲酸甲酯 | 189063-57-8

中文名称
2-氨基-4-乙酰基苯甲酸甲酯
中文别名
——
英文名称
methyl 4-acetyl-2-aminobenzoate
英文别名
4-acetyl-2-amino-benzoic acid methyl ester;4-Acetyl-2-amino-benzoesaeure-methylester
2-氨基-4-乙酰基苯甲酸甲酯化学式
CAS
189063-57-8
化学式
C10H11NO3
mdl
——
分子量
193.202
InChiKey
UHXUFAOTGWYTTA-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:
    372.5±27.0 °C(Predicted)
  • 密度:
    1.198±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    69.4
  • 氢给体数:
    1
  • 氢受体数:
    4

SDS

SDS:73cc63694331760c99d454d40a1ea46d
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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

反应信息

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文献信息

  • Spirocyclopropane compounds. IV. Synthesis of 5-acetylspiro(benzofuran-2(3H),1'-cyclopropan)-3-one related compounds for evaluation as gastric antisecretory and antiulcer agents.
    作者:MASAZUMI WATANABE、MITSURU KAWADA、TAKEO HIRATA、YOSHITAKA MAKI、ISUKE IMADA
    DOI:10.1248/cpb.32.3551
    日期:——
    5-Acetylspiro [benzofuran-2 (3H), 1'-cyclopropan]-3-one (1a) shows potent gastric antisecretory and antiulcer activities in rats. In an attempt to improve the pharmacological profile of 1a, we synthesized positional isomers, as well as the prenyloxy and oxime derivatives. Evaluation of their antisecretory activities and protective activities against gastric lesions induced by water-immersion restraint stress in the rat indicated that the 7-acetyl derivative (1d) was equipotent to 1a.
    5-乙酰基螺[苯并呋喃-2(3H),1'-环丙烷]-3-酮(1a)在大鼠中显示出强大的胃抗分泌和抗溃疡活性。为了改善1a的药理学特性,我们合成了位置异构体以及 prenyl 氧基和肟衍生物。评估它们抗分泌活性以及对大鼠水浸束缚应激诱导的胃损伤的保护作用表明,7-乙酰衍生物(1d)与1a等效。
  • WATANABE, MASAZUMI;KAWADA, MITSURU;HIRATA, TAKEO;MAKI, YOSHITAKA;IMADA, I+, CHEM. AND PHARM. BULL., 1984, 32, N 9, 3551-3560
    作者:WATANABE, MASAZUMI、KAWADA, MITSURU、HIRATA, TAKEO、MAKI, YOSHITAKA、IMADA, I+
    DOI:——
    日期:——
  • COMPOUND HAVING AFFINITY SUBSTANCE TO SOLUBLE PROTEIN, CLEAVABLE PORTION AND REACTIVE GROUP, OR SALT THEREOF
    申请人:Ajinomoto Co., Inc.
    公开号:US20200190165A1
    公开(公告)日:2020-06-18
    The present invention provides a technique enabling modification of a soluble protein and in particular regioselective modification of a soluble protein. More specifically, the present invention provides a compound having an affinity substance to a soluble protein, a cleavable portion, and a reactive group represented by the following Formula (I): A-L-B-R  (I) wherein A is an affinity substance to a soluble protein; L is a cleavable linker which is a divalent group comprising a cleavable portion; B is (a) a divalent group comprising a bioorthogonal functional group or (b) a divalent group comprising no bioorthogonal functional group; and R is a reactive group to the soluble protein; or a salt thereof.
  • Mayer; Stark; Schoen, Chemische Berichte, 1932, vol. 65, p. 1333,1335
    作者:Mayer、Stark、Schoen
    DOI:——
    日期:——
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