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5-羟基-1萘甲酸甲酯 | 91307-40-3

中文名称
5-羟基-1萘甲酸甲酯
中文别名
5-羟基-1-萘甲酸甲酯;氯嘧磺隆
英文名称
methyl 5-hydroxy-1-naphthoate
英文别名
methyl 5-hydroxynaphthalene-1-carboxylate
5-羟基-1萘甲酸甲酯化学式
CAS
91307-40-3
化学式
C12H10O3
mdl
——
分子量
202.21
InChiKey
JXPWWZATUWESQH-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:
    130-131.5℃
  • 沸点:
    368.5±15.0 °C(Predicted)
  • 密度:
    1.264±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2918290000
  • 危险性防范说明:
    P280,P305+P351+P338,P310
  • 危险性描述:
    H302,H315,H319,H332,H335

SDS

SDS:e97f4da9c04572c1e90679744111dcc7
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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

  • 作为反应物:
    描述:
    5-羟基-1萘甲酸甲酯二异丁基氢化铝碘苯二乙酸 作用下, 以 正己烷二氯甲烷乙腈 为溶剂, 反应 0.34h, 以86%的产率得到5-(hydroxymethyl)-1,4-naphthoquinone
    参考文献:
    名称:
    (-)-螺环素 A、C 和 D 的对映选择性全合成
    摘要:
    螺环素 A、C 和 D 是已在海洋真菌菌株 LL-37H248 中鉴定的代谢物。它们独特的多环结构和有趣的生物活性使它们成为合成社区的有吸引力的目标。基于 5-取代萘醌的可扩展对映选择性环氧化、氧化/螺酮缩酮级联、苯酚单元的邻位选择性氯化和肟酯导向的乙酰氧基化、(-)-螺环素 A 和 C 的对映选择性全合成以及已经实现了 (-)-spiroxin D 的首次全合成。
    DOI:
    10.1002/anie.202105921
  • 作为产物:
    描述:
    1-碘-5-甲氧基萘正丁基锂三溴化硼 作用下, 以 四氢呋喃乙醚正己烷二氯甲烷 为溶剂, 反应 16.33h, 生成 5-羟基-1萘甲酸甲酯
    参考文献:
    名称:
    Novel 8-Substituted Dipyridodiazepinone Inhibitors with a Broad-Spectrum of Activity against HIV-1 Strains Resistant to Non-nucleoside Reverse Transcriptase Inhibitors
    摘要:
    A series of novel 8-substituted dipyridodiazepinone-based inhibitors were investigated for their antiviral activity against wild type human immunodeficiency virus (HIV-1) and the clinically prevalent K103N/Y181C mutant virus. Our efforts have resulted in a series of benzoic acid analogues that are potent inhibitors of HIV-1 replication against a panel of HIV-1 strains resistant to non-nucleoside reverse transcriptase inhibitors (NNRTIS). Furthermore, the combination of good antiviral potency, a broad spectrum of activity, and an excellent pharmacokinetic profile provides strong justification for the further development of compound 7 as a potential treatment for wild type and NNRTI-resistant HIV-1 infection.
    DOI:
    10.1021/jm050255t
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文献信息

  • Synthesis of Difluorinated Dihydrobenzo[ <i>de</i> ]chromenes via Rh(III)‐Catalysed C‐H Couplings of 1‐Naphthols with <i>Gem</i> ‐Difluoromethylene Alkynes
    作者:Liping Li、Xiuhua Zhong、Jiali Xu、Hui Gao、Zhi Zhou、Wei Yi
    DOI:10.1002/adsc.202001475
    日期:2021.3.2
    difluorinated dihydrobenzo[de]chromenes with broad substrate/functional group compatibility and good regio‐/chemoselectivity and in an atom‐economic manner. The unique fluorine effects account for the unconventional reaction path involving intramolecular 1,3‐hydrogen migration process to afford the exo‐methylene fragment.
    已经实现了1-萘酚与宝石-二氟亚甲基炔烃的Rh(III)催化的CH偶联,可直接构建具有广泛的底物/官能团相容性和良好的区域/化学选择性的二氟化二氢苯并[ de ]苯二甲基苯。原子经济方式。独特的氟效应解释了涉及分子内1,3-氢迁移过程的非常规反应路径,从而提供了外亚甲基片段。
  • Main-chain donor-acceptor polyhydrazone mediated adsorption of an anionic dye from contaminated water
    作者:Hany F. Nour、Tamer El Malah、Emad K. Radwan、Randa E. Abdel Mageid、Tawfik A. Khattab、Mark A. Olson
    DOI:10.1016/j.reactfunctpolym.2020.104795
    日期:2021.1
    bipyridinium-based dialdehyde (BIPY.2Br DA) in water under acidic conditions (pH, 2–3). The polymeric structure was constructed from alternating units of π-electron rich naphthyl and π-electron deficient bipyridinium (BIPY) moieties linked together via covalent acylhydrazone bonds. Ultraviolet-visible (UV–Vis) absorption analysis confirmed the occurrence of intramolecular donor-acceptor charge transfer (DA-CT) interactions
    通过在水中在酸性条件下(pH )通过四乙二醇连接的三萘基二酰肼与联吡啶基二醛(BIPY.2Br DA)的逐步增长聚合反应,采用一种通用的合成方法来合成聚紫罗兰色(PV.nBr)聚合物。,2–3)。聚合物结构是由π电子富集的萘基和π电子缺乏的联吡啶(BIPY)部分的交替单元通过共价酰基hydr键。紫外线-可见(UV-Vis)吸收分析证实了电子供体和受体单元之间分子内供体-受体电荷转移(DA-CT)相互作用的发生。冻干合成的聚合物以产生具有大表面积和高孔隙率的海绵状气凝胶。扫描电子显微镜(SEM)和透射电子显微镜(TEM)表征表明,冻干后该聚合物在固态下具有均匀的片状形态。在不同的操作条件下研究了这种新型聚合物从合成废水中吸附活性橙122(RO122)染料的能力,并确定其遵循拟一级动力学。结果表明,新型PV。nBr可以在宽范围的溶液pH值下高效快速地去除RO122,吸收率高达97%。新型PV.
  • GRAM-POSITIVE CARBAPENEM ANTIBACTERIALS AND PROCESSES FOR THEIR PREPARATION
    申请人:Choi Woo-Baeg
    公开号:US20100075945A1
    公开(公告)日:2010-03-25
    The present invention provides β-methyl carbapenem compounds and pharmaceutical compositions useful in the treatment of bacterial infections and methods for treating such infections using such compounds and/or compositions. The invention includes administering an effective amount of a carbapenem compound or salt and/or prodrug thereof to a host in need of such a treatment. The present invention is also in the field of synthetic organic chemistry and is specifically provides an improved method of synthesis of β-methyl carbapenems which are useful as antibacterial agents.
    本发明提供了β-甲基碳青霉烯化合物和制药组合物,可用于治疗细菌感染,并提供使用这些化合物和/或组合物治疗此类感染的方法。本发明包括向需要此类治疗的宿主投与有效量的碳青霉烯化合物或盐和/或前药。本发明还属于合成有机化学领域,特别提供了一种改进的β-甲基碳青霉烯化合物合成方法,该方法可用作抗菌剂。
  • Method of producing thermotropic liquid crystalline polyester
    申请人:MITSUBISHI CHEMICAL CORPORATION
    公开号:EP0520428A2
    公开(公告)日:1992-12-30
    A thermotropic liquid crystalline polyester is produced by carrying out polycondensation of ester monomer [I-2], an aromatic dicarboxylic acid [II] and an aromatic carboxylic acid [III-2]. The amounts of the compounds [I-2] and [II] are substantially equivalent and the amount of the compound [III-2] is not more than 20 times that of [I-2] by mole. A thermotropic liquid crystalline polyester having good heat resistance, fluidity and uniformity can be produced.
    通过酯单体[I-2]、芳香族二羧酸[II]和芳香族羧酸[III-2]的缩聚反应,生产出一种热致性液晶聚酯。化合物[I-2]和[II]的量基本相等,化合物[III-2]的量不超过[I-2]的 20 倍(以摩尔计)。这样就可以生产出具有良好耐热性、流动性和均匀性的热致性液晶聚酯。
  • Quinoidation of Triaryl Compounds—Hydroxynaphthyldiphenylcarbinols
    作者:Leigh C. Anderson、Donald G. Thomas
    DOI:10.1021/ja01242a027
    日期:1943.2
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