2363-23-7 ((Benzene,1-(methylthio)-2,4-dinitro-)

CAS号:
2363-23-7
英文名称:
Benzene,1-(methylthio)-2,4-dinitro-
分子式:
C7H6N2O4S
分子量:
214.198540210724

Benzene,1-(methylthio)-2,4-dinitro-(2363-23-7)名称与标识符

名称

英文别名:
Benzene,1-(methylthio)-2,4-dinitro-;1-methylsulfanyl-2,4-dinitrobenzene;(2,4-dinitro-phenyl)-methyl sulfide;(2,4-Dinitro-phenyl)-methyl-sulfid;1-Methylmercapto-2,4-dinitrobenzene;1-Methylthio-2,4-dinitrobenzene;2,4-Dinitro-1-(methylthio)benzene;2,4-Dinitrothioanisole;2.4-Dinitro-1-methylmercapto-benzol;2.4-Dinitro-thioanisol;methyl 2,4-dinitriophenyl sulfide;Methyl 2,4-dinitrophenyl sulfide;Sulfide,2,4-dinitrophenyl methyl;Benzene, 2,4-dinitro-1-(methylthio)- (9CI);1-(methylthio)-2,4-dinitrobenzene;Benzene, 2,4-dinitro-1-(methylthio)-;Benzene, 1-(methylthio)-2,4-dinitro-;DTXSID30178302;2363-23-7;BRN 2054390;UNII-RBN9L8V33S;CCRIS 1804;2,4-Dinitrophenyl methyl sulfide;RBN9L8V33S;SCHEMBL8973665;NSC-25819;NSC25819;AKOS003235646;1-Methylsulfanyl-2,4-dinitro-benzene;NSC 25819;Sulfide, 2,4-dinitrophenyl methyl;

标识符

InChIKey:
CQLUVMHXDVLHSK-UHFFFAOYSA-N
Inchi:
1S/C7H6N2O4S/c1-14-7-3-2-5(8(10)11)4-6(7)9(12)13/h2-4H,1H3
SMILES:
S(C)C1C=CC(=CC=1[N+](=O)[O-])[N+](=O)[O-]

Benzene,1-(methylthio)-2,4-dinitro-(2363-23-7)物化性质

实验特性

  • LogP : 3.27130
  • PSA : 116.94000
  • 折射率 : 1.631
  • 沸点 : 342°C at 760 mmHg
  • 闪点 : 160.6°C
  • 密度 : 1.48

计算特性

  • 精确分子量 : 214.00500
  • 氢键供体数量 : 0
  • 氢键受体数量 : 5
  • 可旋转化学键数量 : 1
  • 同位素质量 : 214.005
  • 重原子数量 : 14
  • 复杂度 : 237
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 2
  • 拓扑分子极性表面积 : 117Ų

Benzene,1-(methylthio)-2,4-dinitro-(2363-23-7)上下游

Benzene,1-(methylthio)-2,4-dinitro-(2363-23-7)相关文献

  • 1. 591. Oxidation of organic sulphides. Part VII. The mechanism of autoxidation of but-2-enyl methyl sulphide, methyl 1-methylbut-2-enyl sulphide, and n-butyl methyl sulphide
    L. Bateman,J. I. Cunneen,J. Ford J. Chem. Soc. 1956 3056
  • 2. Photolysis of compounds containing an o-nitroarylthio-substituent
    R. S. Goudie,P. N. Preston J. Chem. Soc. C 1971 3081
  • 3. Oxidation of organic sulphides. Part IV. Autoxidation of cyclohex-2-enyl methyl sulphide
    L. Bateman,F. W. Shipley J. Chem. Soc. 1955 1996
  • 4. 578. The structure of “isothiohydantoin” and related compounds
    W. Davies,J. A. Maclaren J. Chem. Soc. 1951 2595
  • 5. Kinetics and mechanism of oxidation of 2,4-dinitrophenylhydrazine, p-nitrophenylhydrazine, and p-tolylhydrazine with potassium hexacyanoferrate(III) in acidic perchlorate media
    Ashok K. Gupta,Bharati Gupta,Abhay K. Gupta,Yugul K. Gupta J. Chem. Soc. Dalton Trans. 1984 2599