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2-methylthio-3,5-dimethylphenol | 25674-57-1

中文名称
——
中文别名
——
英文名称
2-methylthio-3,5-dimethylphenol
英文别名
2-Metiltio-3,5-dimetil-fenolo;3,5-dimethyl-2-methylsulfanylphenol
2-methylthio-3,5-dimethylphenol化学式
CAS
25674-57-1
化学式
C9H12OS
mdl
——
分子量
168.26
InChiKey
DGLPDVONIWDUPH-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:
    132-133 °C(Press: 15 Torr)
  • 密度:
    1.12±0.1 g/cm3(Predicted)
  • 溶解度:
    可溶于氯仿(少许)、甲醇(少许)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    45.5
  • 氢给体数:
    1
  • 氢受体数:
    2

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

  • 作为产物:
    参考文献:
    名称:
    Electrochemically generated organothiating reagents and their use
    摘要:
    在液态二氧化硫中电解有机二硫化物可获得有机硫化剂,然后可与适当底物反应,高效合成有机硫代芳香化合物,并且产率高。与适当酚类化合物反应时,会发生区域选择性取代,其中对位取代远远超过邻位取代。
    公开号:
    US06207838B1
点击查看最新优质反应信息

文献信息

  • 3-phenoxy-4-pyridazinol derivatives and herbicide composition containing the same
    申请人:Tsukamoto Yoshihisa
    公开号:US20050037925A1
    公开(公告)日:2005-02-17
    A compound represented by the formula: [wherein R 1 represents a hydrogen atom, a halogen, atom, alkyl group, etc., R 2 represents a hydrogen atom, a halogen atom, alkyl group, etc., R 3 , R 4 , R 5 , R 6 and R 7 each independently represent a hydrogen atom, a halogen atom, a substitutable alkyl group, a substitutable alkenyl group, alkynyl group, a substituteable cycloalkyl group, etc., or R 3 , R 4 , R 5 , R 6 and R 7 may form a ring which may be substituted, which is formed by the adjacent two of them with carbon atoms to which the respective substituents are bonded, m and n each independently represent 0 or 1.] a salt thereof, an ester derivative thereof and an agricultural chemical containing the same as an effective ingredient, and a herbicidal composition containing the compound and a second herbicidally active compound as effective ingredients.
    一种化合物由以下式子表示:[其中R1代表氢原子,卤素原子,烷基团等,R2代表氢原子,卤素原子,烷基团等,R3,R4,R5,R6和R7各自独立地代表氢原子,卤素原子,可替换的烷基团,可替换的烯基团,炔基团,可替换的环烷基团等,或R3,R4,R5,R6和R7可以形成一个环,该环可以被取代,该环由相邻的两个碳原子形成,这些碳原子与相应的取代基团相连,m和n各自独立地代表0或1。]其盐,酯衍生物及含有该化合物为有效成分的农药,以及含有该化合物和第二种草甘膦活性化合物为有效成分的除草剂组合物。
  • 3-Phenoxy-4-pyridazinol derivatives and herbicidal composition containing the same
    申请人:Tsukamoto Yoshihisa
    公开号:US20100041555A1
    公开(公告)日:2010-02-18
    A compound represented by the formula: [wherein R 1 represents a hydrogen atom, a halogen atom, alkyl group, etc., R 2 represents a hydrogen atom, a halogen atom, alkyl group, etc., R 3 , R 4 , R 5 , R 6 and R 7 each independently represent a hydrogen atom, a halogen atom, a substitutable alkyl group, a substitutable alkenyl group, alkynyl group, a substitutable cycloalkyl group, etc., or R 3 , R 4 , R 5 , R 6 and R 7 may form a ring which may be substituted, which is formed by the adjacent two of them with carbon atoms to which the respective substituents are bonded, m and n each independently represent 0 or 1.] a salt thereof, an ester derivative thereof and an agricultural chemical containing the same as an effective ingredient, and a herbicidal composition containing the compound and a second herbicidally active compound as effective ingredients.
    一种化合物,其化学式为:[其中R1代表氢原子、卤素原子、烷基等,R2代表氢原子、卤素原子、烷基等,R3、R4、R5、R6和R7各自独立地代表氢原子、卤素原子、可替换的烷基、可替换的烯基、炔基、可替换的环烷基等,或R3、R4、R5、R6和R7可形成一个环,该环可以被取代,由它们中的相邻两个碳原子形成,各自带有相应的取代基,m和n各自独立地代表0或1。]其盐、酯衍生物和含有该化合物作为有效成分的农药,以及含有该化合物和第二种除草活性化合物作为有效成分的除草剂组合物。
  • 3-PHENOXY-4-PYRIDAZINOL DERIVATIVE AND HERBICIDE COMPOSITION CONTAINING THE SAME
    申请人:MITSUI CHEMICALS AGRO, INC.
    公开号:EP1426365B9
    公开(公告)日:2009-10-21
  • Electrochemical electrophilic aromatic methylthiation in liquid SO2
    作者:Richard S. Glass、Viatcheslav V. Jouikov
    DOI:10.1016/s0040-4039(99)01311-8
    日期:1999.8
    Controlled potential electrolysis of dimethyldisulfide in liquid sulfur dioxide provides a strongly electrophilic methylthiating agent. This species methylthiates strongly to weakly activated arenes in good to excellent yield. (C) 1999 Elsevier Science Ltd. All rights reserved.
  • Cabiddu,S. et al., Gazzetta Chimica Italiana, 1969, vol. 99, p. 1095 - 1106
    作者:Cabiddu,S. et al.
    DOI:——
    日期:——
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