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2-(2,4-二溴苯氧基)乙酰氯 | 16738-07-1

中文名称
2-(2,4-二溴苯氧基)乙酰氯
中文别名
——
英文名称
2,4-dibromophenoxyacetyl chloride
英文别名
(2,4-Dibromophenoxy)acetyl chloride;2-(2,4-dibromophenoxy)acetyl chloride
2-(2,4-二溴苯氧基)乙酰氯化学式
CAS
16738-07-1
化学式
C8H5Br2ClO2
mdl
MFCD11107988
分子量
328.387
InChiKey
ABJOJUXBOIRTBS-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:
    331.5±27.0 °C(Predicted)
  • 密度:
    1.922±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2918990090

SDS

SDS:e4a7f80851edb6100f89c8bf32e8f473
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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:
    吩噻嗪2-(2,4-二溴苯氧基)乙酰氯sodium hydroxide 作用下, 以 甲醇乙醚乙酸乙酯 为溶剂, 以70%的产率得到10H-Phenothiazine, 10-((2,4-dibromophenoxy)acetyl)-
    参考文献:
    名称:
    Chaurasia; Srivastava, Journal of the Indian Chemical Society, 1991, vol. 68, # 2, p. 106 - 107
    摘要:
    DOI:
  • 作为产物:
    描述:
    sodium 2,4-dibromophenolate 在 氯化亚砜 作用下, 以 乙酸乙酯 为溶剂, 反应 8.0h, 生成 2-(2,4-二溴苯氧基)乙酰氯
    参考文献:
    名称:
    Chaurasia, Sunita; Srivastava, Savitri D., Journal of the Indian Chemical Society, 1992, vol. 69, # 1, p. 45 - 46
    摘要:
    DOI:
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文献信息

  • Srivastava; Purohit; Srivastava, Journal of the Indian Chemical Society, 1991, vol. 68, # 6, p. 358 - 359
    作者:Srivastava、Purohit、Srivastava、Jain、Khubchandani
    DOI:——
    日期:——
  • Studies of <i>O</i>,<i>O</i>-Dimethyl α-(2,4-Dichlorophenoxyacetoxy)ethylphosphonate (HW02) as a New Herbicide. 1. Synthesis and Herbicidal Activity of HW02 and Analogues as Novel Inhibitors of Pyruvate Dehydrogenase Complex
    作者:Hong-Wu He、Jun-Lin Yuan、Hao Peng、Ting Chen、Ping Shen、Shu-Qing Wan、Yanjun Li、Hong-Liang Tan、Ya-Hui He、Jun-Bo He、Yan Li
    DOI:10.1021/jf104247w
    日期:2011.5.11
    On the basis of the previous work for optimization of O,O-diethyl alpha-(substituted phenoxyacetoxy)alkylphosphonates, further extensive synthetic modifications were made to the substituents in alkylphosphonate and phenoxy moieties of the title compounds. New O,O-dimethyl alpha-(substituted phenoxyacetoxy)alkylphosphonates were synthesized as potential inhibitors of pyruvate dehydorogenase complex (PDHc). Their herbicidal activity and efficacy in vitro against PDHc were examined. Some of these compounds exhibited significant herbicidal activity and were demonstrated to be effective inhibitors of PDHc from three different plants. The structure-activity relationships of these compounds including previously reported analogous compounds were studied by examining their herbicidal activities. Both inhibitory potency against PDHc and herbicidal activity of title compounds could be increased greatly by optimizing substituent groups of the title compounds. O,O-Dimethyl alpha-(2,4-dichlorophenoxyacetoxy)ethylphosphonate (I-5), which acted as a competitive inhibitor of PDHc with much higher inhibitory potency against PDHc from Pisum sativum and Phaseolus radiatus than from Oryza sativa , was found to be the most effective compound against broadleaf weeds and showed potential utility as herbicide.
  • Purohit; Srivastava, Journal of the Indian Chemical Society, 1991, vol. 68, # 3, p. 163 - 165
    作者:Purohit、Srivastava
    DOI:——
    日期:——
  • Bhatt, P.; Srivastava, S. D.; Mehta, P., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1998, vol. 37, # 5, p. 514 - 516
    作者:Bhatt, P.、Srivastava, S. D.、Mehta, P.
    DOI:——
    日期:——
  • Chaurasia, Sunita; Srivastava, Savitri D., Journal of the Indian Chemical Society, 1992, vol. 69, # 1, p. 45 - 46
    作者:Chaurasia, Sunita、Srivastava, Savitri D.
    DOI:——
    日期:——
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