2243-78-9 (([1,1'-Biphenyl]-4,4'-diamine,2-nitro-)

快速询单

结构式：

[1,1'-Biphenyl]-4,4'-diamine,2-nitro-MOL文件

CAS号：

2243-78-9

英文名称：

[1,1'-Biphenyl]-4,4'-diamine,2-nitro-

分子式：

C₁₂H₁₁N₃O₂

分子量：

229.234642267227

[1,1'-Biphenyl]-4,4'-diamine,2-nitro-(2243-78-9)名称与标识符

名称

英文别名：

[1,1'-Biphenyl]-4,4'-diamine,2-nitro-;2-Nitro-benzidin;2-nitro-benzidine;3-nitro-4,4'-diaminobiphenyl;4,4'-Diamino-2-nitrobiphenyl;Benzidine,2-nitro;nitro-2 benzidine;4-(4-AMINOPHENYL)-3-NITRO-ANILINE;UNII-C104KU8407;2-Nitrobenzidine;Q27894110;AKOS004903537;BRN 2736686;2-Nitrobenzidin;2243-78-9;DTXSID4036859;2-Nitrobenzidin [Czech];3-13-00-00449 (Beilstein Handbook Reference);4-(4-aminophenyl)-3-nitroaniline;SCHEMBL474215;(1,1'-BIPHENYL)-4,4'-DIAMINE, 2-NITRO-;2-NITRO(1,1'-BIPHENYL)-4,4'-DIAMINE;CCRIS 6586;Nitrobenzidin;2-Nitro-[1,1'-biphenyl]-4,4'-diamine;C104KU8407;Benzidine, 2-nitro-;

标识符

MDL：

MFCD00025340

InChIKey：

YYNCOERMULFLJD-UHFFFAOYSA-N

Inchi：

1S/C12H11N3O2/c13-9-3-1-8(2-4-9)11-6-5-10(14)7-12(11)15(16)17/h1-7H,13-14H2

SMILES：

[O-][N+](C1C=C(C=CC=1C1C=CC(=CC=1)N)N)=O

[1,1'-Biphenyl]-4,4'-diamine,2-nitro-(2243-78-9)物化性质

实验特性

LogP : 4.11180
PSA : 97.86000

计算特性

精确分子量 : 229.08500
氢键供体数量 : 2
氢键受体数量 : 2
可旋转化学键数量 : 2
同位素质量 : 229.085126602g/mol
重原子数量 : 17
复杂度 : 271
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 : 97.9Å²

[1,1'-Biphenyl]-4,4'-diamine,2-nitro-(2243-78-9)海关数据

海关编码：

2921590090

海关数据：

中国海关编码：

2921590090

概述：

2921590090. 其他芳香多胺及衍生物及它们的盐. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%

申报要素：

品名, 成分含量, 用途

Summary：

2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

[1,1'-Biphenyl]-4,4'-diamine,2-nitro-(2243-78-9)上下游

4,4-二溴-2-硝基-联苯 3,8-双-(乙氧基羰氨基)-6-苯菲啶硫酸联苯胺

[1,1'-Biphenyl]-4,4'-diamine,2-nitro-(2243-78-9)相关文献

1. CCLXXIV.—Orientation effects in the diphenyl series. Part III. The mononitro-4 : 4′-dihalogenodiphenyls and some allied compounds
Raymond James Wood Le Fèvre,Eustace Ebenezer Turner J. Chem. Soc. 1926 129 2041
2. Orientation effects in the diphenyl series. Part XIV. The thermal decomposition of some “diazoperbromides”
Shiu May Loh,E. E. Turner J. Chem. Soc. 1955 1274
3. 377. The optical activity of a diphenyl derivative, the dissymmetry of which is caused by the space effect of only one group
Mary S. Lesslie,Eustace E. Turner J. Chem. Soc. 1933 1588
4. 40. Orientation effects in the diphenyl series. Part X. The quantitative nitration of 4 : 4′-dichloro- and 4 : 4′-dibromo-diphenyl and of 4-chloro- 4′-bromodiphenyl
Florence Ruth Shaw,Eustace Ebenezer Turner J. Chem. Soc. 1932 285
5. 47. Potential trypanocides of the N-heterocyclic series. Part I. Phenanthridinium salts
A. G. Caldwell,L. P. Walls J. Chem. Soc. 1948 188
6. CXLVII.—Orientation effects in the diphenyl series. Part VIII. The nitration of 4 : 4′-difluorodiphenyl
Raymond James Wood Le Fèvre,Eustace Ebenezer Turner J. Chem. Soc. 1930 1158
7. XLVIII.—Studies in the diphenyl series. Part I. Acetylation of benzidine derivatives
John Cannell Cain,Percy May J. Chem. Soc. Trans. 1910 97 720
8. 622. Mesomorphism and chemical constitution. Part XII. The preparation and mesomorphic properties of substituted 4,4′-di-(p-n-alkoxybenzylideneamino)biphenyls
S. J. Branch,D. J. Byron,G. W. Gray,A. Ibbotson,B. M. Worrall J. Chem. Soc. 1964 3279
9. LXI.—Orientation effects in the diphenyl series. Part I
Henry George Dennett,Eustace Ebenezer Turner J. Chem. Soc. 1926 129 476
10. CCXLII.—Studies in the diphenyl series. Part II. The dinitrobenzidines: a new form of isomerism
John Cannell Cain,Albert Coulthard,Frances Mary Gore Micklethwait J. Chem. Soc. Trans. 1912 101 2298

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