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4-(4-methoxy-2,5-dimethylphenyl)butanoic acid | 4705-97-9

中文名称
——
中文别名
——
英文名称
4-(4-methoxy-2,5-dimethylphenyl)butanoic acid
英文别名
4-(4-methoxy-2,5-dimethyl-phenyl)-butyric acid;4-(4-Methoxy-2,5-dimethyl-phenyl)-buttersaeure;γ-(4-Methoxy-2.5-dimethyl-phenyl)-buttersaeure;4--buttersaeure
4-(4-methoxy-2,5-dimethylphenyl)butanoic acid化学式
CAS
4705-97-9
化学式
C13H18O3
mdl
——
分子量
222.284
InChiKey
XOBZQMGCZYSQEJ-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):
    2.7
  • 重原子数:
    16
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险等级:
    IRRITANT

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:
    参考文献:
    名称:
    设计,构象和晶体学的2-萘苯基苯基醚作为有效的抗艾滋病毒剂
    摘要:
    据报道,掺有7-氰基-2-萘基取代基的邻苯二酚二醚是HIV-1逆转录酶(NNRTIs)的非核苷抑制剂。许多化合物对野生型HIV-1的效价为1-10 nM。一个有趣的构象效应使得与HIV-RT形成复合物的萘基具有两个独特的构象体。4a和4f的X射线晶体结构说明了替代方案。
    DOI:
    10.1021/acsmedchemlett.6b00390
  • 作为产物:
    描述:
    2,5-二甲基苯酚盐酸三氯化铝 、 amalgamated zinc 、 作用下, 生成 4-(4-methoxy-2,5-dimethylphenyl)butanoic acid
    参考文献:
    名称:
    A patient with type I CD36 deficiency whose myocardium accumulated123I-BMIPP after 4 years
    摘要:
    A 73-year-old man with aortic regurgitation was examined by I-123-alpha -methyl-p-iodophenylpentadecanoic acid (BMIPP) myocardial single photon emission computed tomography (SPECT) in 1995. Myocardial accumulation was not evident on either the early or the delayed image obtained 15 minutes and 3 hours, respectively, after injecting I-123-BMIPP. Flow cytometric analysis of CD36 expression in monocytes and platelets identified a type I CD36 deficiency. The patient was hospitalized for severe heart failure in 1999. Upon admission, the cardiothoracic ratio on chest Xrays was 73%, and the left ventricular end-diastolic diameter on echocardiograms was enlarged to 77 mm. On the second day, we performed I-123-BMIPP myocardial SPECT. Myocardial accumulation was evident in the delayed, but not in the early image. We repeated I-123-BMIPP myocardial SPECT on the 10th day after admission. Myocardial accumulation was evident on both early and delayed images. Tc-99m-tetrofosmin myocardial SPECT was immediately performed after I-123-BMIPP myocardial SPECT to distinguish myocardial from pooling images in the left ventricle, but, because the images from both 99mTc-tetrofosmin and I-123-BMIPP myocardial SPECT were idential, we considered that the 123I-BMIPP myocardial SPECT images reflected the actual myocardial condition.The CD36 molecule transports long-chain fatty acid (LCFA) on the myocardial membrane, but I-123-BMIPP scintigraphy does not show any myocardial accumulation in patients with type I CD36 deficiency, indicating that myocardial LCFA uptake occurs through CD36 on the human myocardial membrane. Even though our patient had type I CD36 deficiency, BMIPP was uptaken by the myocardium during heart failure, suggesting a variant pathway on the human myocardial membrane for LCFA uptake.
    DOI:
    10.1007/bf02987845
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文献信息

  • Photochemical rearrangements of cross-conjugated cyclohexadienones—VII
    作者:P.J. Kropp
    DOI:10.1016/s0040-4020(01)98355-3
    日期:1965.1
    concerning its intermediacy in the previously reported rearrangement of the dienone (I) to the linearly conjugated isomer (IX). The spiro dienone (VIII) was prepared by solvolysis of the tosylate (XVI). On irradiation in methanol or dioxane it was converted principally to the cyclopropyl ketone (IV), which, in turn, underwent further rearrangement to the dienone (IX). No evidence for the formation of
    为了在先前报道的二烯酮(I)重排成线性共轭异构体(IX)的过程中获得有关其中间体的证据,已经研究了螺二烯酮(VIII)在中性介质中的光化学行为。螺二烯酮(VIII)是通过甲苯磺酸酯(XVI)的溶剂化制备的。在甲醇或二恶烷中照射后,它主要转化为环丙基酮(IV),然后进一步重排为二烯酮(IX)。未检测到形成异构体环丙基酮(XI)的证据。建议光产物(IV)的选择性形成归因于IV的β-甲基取代的烯酮体系相对于α-甲基异构体(XI)的稳定性增强。
  • A Modification of the Clemmensen Method of Reduction<sup>1</sup>
    作者:Elmore L. Martin
    DOI:10.1021/ja01299a038
    日期:1936.8
  • Clemo; Haworth; Walton, Journal of the Chemical Society, 1929, p. 2383
    作者:Clemo、Haworth、Walton
    DOI:——
    日期:——
  • Ashok, K.; Rao, G.S. Krishna, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1993, vol. 32, # 10, p. 1013 - 1017
    作者:Ashok, K.、Rao, G.S. Krishna
    DOI:——
    日期:——
  • Fetizon,M.; Nguyen Trong Anh, Bulletin de la Societe Chimique de France, 1965, p. 3208 - 3210
    作者:Fetizon,M.、Nguyen Trong Anh
    DOI:——
    日期:——
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