摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1,3-benzothiazol-2-yl(phenyl)phosphinic acid | 262603-86-1

中文名称
——
中文别名
——
英文名称
1,3-benzothiazol-2-yl(phenyl)phosphinic acid
英文别名
——
1,3-benzothiazol-2-yl(phenyl)phosphinic acid化学式
CAS
262603-86-1
化学式
C13H10NO2PS
mdl
——
分子量
275.268
InChiKey
CFIXGBMNAXHWEK-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:
    474.0±28.0 °C(Predicted)
  • 密度:
    1.44±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    78.4
  • 氢给体数:
    1
  • 氢受体数:
    4

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:
    Direct Phosphorylation of Benzothiazoles and 4-Methyltthiazole
    摘要:
    Simple procedures for preparation of 2-(4-methylthiazolyl) dichlorophosphine and wide variety of 2-phosphorylated benzothiazoles are reported. Efficient promoters and catalysts were found for the key transformation, direct phosphorylation of the heterocyclic compounds by PCl3 (PBr3 as a promoter) or by P(V) acid chlorides (HgCl2 as a catalyst).
    DOI:
    10.1080/00397910008087315
  • 作为产物:
    描述:
    苯膦酰二氯苯并噻唑三乙胺 、 mercury dichloride 作用下, 以 吡啶 为溶剂, 以69%的产率得到1,3-benzothiazol-2-yl(phenyl)phosphinic acid
    参考文献:
    名称:
    Direct Phosphorylation of Benzothiazoles and 4-Methyltthiazole
    摘要:
    Simple procedures for preparation of 2-(4-methylthiazolyl) dichlorophosphine and wide variety of 2-phosphorylated benzothiazoles are reported. Efficient promoters and catalysts were found for the key transformation, direct phosphorylation of the heterocyclic compounds by PCl3 (PBr3 as a promoter) or by P(V) acid chlorides (HgCl2 as a catalyst).
    DOI:
    10.1080/00397910008087315
点击查看最新优质反应信息

文献信息

  • POLYMER ELECTROLYTE COMPOSITION AND POLYMER ELECTROLYTE MEMBRANE, MEMBRANE-ELECTROLYTE ASSEMBLY, AND SOLID POLYMER FUEL CELL USING SAME
    申请人:Toray Industries, Inc.
    公开号:EP3131145A1
    公开(公告)日:2017-02-15
    [Problem] To provide: a polymer electrolyte composition that has excellent chemical stability that makes it possible to withstand a strong oxidizing atmosphere during fuel cell operation, that makes it possible to achieve excellent protonic conductivity under low humidity conditions, excellent mechanical strength, and excellent physical durability, and that is highly practical; and a polymer electrolyte membrane, a membrane-electrode assembly, and a solid polymer fuel cell that use the polymer electrolyte composition. [Solution] A polymer electrolyte composition that comprises at least an ionic group-containing polymer (A), an organic phosphorus-based additive (C), and a nitrogen-containing heteroaromatic ring system additive (D) and that is characterized by the nitrogen-containing heteroaromatic ring system additive (D) comprising at least three nitrogen-containing heteroaromatic rings within a molecule thereof. In addition, the polymer electrolyte membrane, the catalyst layer-equipped electrolyte membrane, the membrane-electrode assembly, and the solid polymer fuel cell of the present invention are characterized by being configured using the polymer electrolyte composition.
    问题 提供一种聚合物电解质组合物,该组合物具有优异的化学稳定性,能够在燃料电池运行期间耐受强氧化性气氛,能够在低湿度条件下实现优异的质子电导率,具有优异的机械强度和优异的物理耐久性,并且具有很高的实用性;以及一种使用该聚合物电解质组合物的聚合物电解质膜、膜电极组件和固体聚合物燃料电池。[解决方案]一种聚合物电解质组合物,它至少包含一种含离子基团的聚合物(A)、一种有机磷基添加剂(C)和一种含氮杂芳香族环系添加剂(D),其特征在于含氮杂芳香族环系添加剂(D)在其分子内至少包含三个含氮杂芳香族环。此外,本发明的聚合物电解质膜、配备催化剂层的电解质膜、膜电极组件和固体聚合物燃料电池的特征在于使用聚合物电解质组合物进行配置。
  • Direct Phosphorylation of Benzothiazoles and 4-Methyltthiazole
    作者:Igor V. Komarov、Aleksandr V. Strizhak、Mikhail Yu. Kornilov、Evgeniy Zarudnitskiy、Andrey A. Tolmachev
    DOI:10.1080/00397910008087315
    日期:2000.1
    Simple procedures for preparation of 2-(4-methylthiazolyl) dichlorophosphine and wide variety of 2-phosphorylated benzothiazoles are reported. Efficient promoters and catalysts were found for the key transformation, direct phosphorylation of the heterocyclic compounds by PCl3 (PBr3 as a promoter) or by P(V) acid chlorides (HgCl2 as a catalyst).
查看更多

同类化合物

(1Z)-1-(3-乙基-5-羟基-2(3H)-苯并噻唑基)-2-丙酮 齐拉西酮砜 阳离子蓝NBLH 阳离子荧光黄4GL 锂2-(4-氨基苯基)-5-甲基-1,3-苯并噻唑-7-磺酸酯 铜酸盐(4-),[2-[2-[[2-[3-[[4-氯-6-[乙基[4-[[2-(硫代氧代)乙基]磺酰]苯基]氨基]-1,3,5-三嗪-2-基]氨基]-2-(羟基-kO)-5-硫代苯基]二氮烯基-kN2]苯基甲基]二氮烯基-kN1]-4-硫代苯酸根(6-)-kO]-,(1:4)氢,(SP-4-3)- 铜羟基氟化物 钾2-(4-氨基苯基)-5-甲基-1,3-苯并噻唑-7-磺酸酯 钠3-(2-{(Z)-[3-(3-磺酸丙基)-1,3-苯并噻唑-2(3H)-亚基]甲基}[1]苯并噻吩并[2,3-d][1,3]噻唑-3-鎓-3-基)-1-丙烷磺酸酯 邻氯苯骈噻唑酮 西贝奈迪 螺[3H-1,3-苯并噻唑-2,1'-环戊烷] 螺[3H-1,3-苯并噻唑-2,1'-环己烷] 葡萄属英A 草酸;N-[1-[4-(2-苯基乙基)哌嗪-1-基]丙-2-基]-2-丙-2-基氧基-1,3-苯并噻唑-6-胺 苯酰胺,N-2-苯并噻唑基-4-(苯基甲氧基)- 苯酚,3-[[2-(三苯代甲基)-2H-四唑-5-基]甲基]- 苯胺,N-(3-苯基-2(3H)-苯并噻唑亚基)- 苯碳杂氧杂脒,N-1,2-苯并异噻唑-3-基- 苯甲基2-甲基哌啶-1,2-二羧酸酯 苯并噻唑正离子,2-[3-(1,3-二氢-1,3,3-三甲基-2H-吲哚-2-亚基)-1-丙烯-1-基]-3-乙基-,碘化(1:1) 苯并噻唑正离子,2-[(2-乙氧基-2-羰基乙基)硫代]-3-甲基-,溴化 苯并噻唑啉 苯并噻唑-d4 苯并噻唑-6-腈 苯并噻唑-5-羧酸 苯并噻唑-5-硼酸频哪醇酯 苯并噻唑-4-醛 苯并噻唑-4-乙酸 苯并噻唑-2-磺酸钠 苯并噻唑-2-磺酸 苯并噻唑-2-磺酰氟 苯并噻唑-2-甲醛 苯并噻唑-2-甲酸 苯并噻唑-2-甲基甲胺 苯并噻唑-2-基磺酰氯 苯并噻唑-2-基叠氮化物 苯并噻唑-2-基-邻甲苯-胺 苯并噻唑-2-基-己基-胺 苯并噻唑-2-基-(4-氯-苯基)-胺 苯并噻唑-2-基-(4-氟-苯基)-胺 苯并噻唑-2-基-(4-乙氧基-苯基)-胺 苯并噻唑-2-基-(2-甲氧基-苯基)-胺 苯并噻唑-2-基-(2,6-二甲基-苯基)-胺 苯并噻唑-2-基(对甲苯基)甲醇 苯并噻唑-2-乙酸甲酯 苯并噻唑-2-乙腈 苯并噻唑-2(3H)-酮N2-[1-(吡啶-4-基)乙亚基]腙 苯并噻唑-2 - 丙基 苯并噻唑,6-(3-乙基-2-三氮烯基)-2-甲基-(8CI)