16033-21-9 ((1-Triazene,1-methyl-3-phenyl-)

快速询单

结构式：

1-Triazene,1-methyl-3-phenyl-MOL文件

CAS号：

16033-21-9

英文名称：

1-Triazene,1-methyl-3-phenyl-

分子式：

C₇H₉N₃

分子量：

135.166460752487

1-Triazene,1-methyl-3-phenyl-(16033-21-9)名称与标识符

名称

英文别名：

1-Triazene,1-methyl-3-phenyl-;3-Methyl-1-phenyltriazene;N-(methyldiazenyl)aniline;1-Methyl-3-phenyltriazene;1-Phenyl-3-methyl-triazen;1-phenyl-3-methyltriazene;1-Phenyl-3-monomethyltriazene;3-Methyl-1-phenyl-triazen;3-Methyl-1-phenyltriazine;Methylaminoazobenzene;Methylphenyltriazene;N-Methyl-N'-phenyl-triazen;N-methyl-N'-phenyl-triazene;Phenylmonomethyltriazene;PMMT;Triazene, 3-methyl-1-phenyl-;Triazene, 3-monomethyl-1-phenyl-;AKOS006279617;Phenyl-mono-methyl-triazen;NSC136056;SCHEMBL22263150;16033-21-9;1-methyl-3-phenyl-1-triazene;Triazene, 1-methyl-3-phenyl-;NSC 136056;1-Phenyl-3-monomethyl-triazene;1-Triazene, 1-methyl-3-phenyl-;DTXSID50166862;CHEMBL121569;1-Phenyl-3-methyltriazine;WLN: 1MNUNR;NSC-136056;SCHEMBL9119900;

标识符

InChIKey：

MPEZFYGMDYORDA-UHFFFAOYSA-N

Inchi：

1S/C7H9N3/c1-8-10-9-7-5-3-2-4-6-7/h2-6H,1H3,(H,8,9)

SMILES：

N(C1C=CC=CC=1)/N=N/C

1-Triazene,1-methyl-3-phenyl-(16033-21-9)物化性质

实验特性

PSA : 36.75
折射率 : 1.5400 (estimate)
沸点 : 238.87°C (rough estimate)
闪点 : 71.3°C
密度 : 1.1423 (rough estimate)

计算特性

精确分子量 : 135.07977
氢键供体数量 : 1
氢键受体数量 : 3
可旋转化学键数量 : 2
同位素质量 : 135.08
重原子数量 : 10
复杂度 : 105
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） : 2.4
拓扑分子极性表面积 : 36.8A^2

1-Triazene,1-methyl-3-phenyl-(16033-21-9)相关文献

1. Photochemical decomposition of 2,4-dinitro-4′-dimethylaminoazobenzene in aerated solution
Angelo Albini,Elisa Fasani,Silvio Pietra J. Chem. Soc. Perkin Trans. 2 1986 681
2. C.—Additive compounds of trinitrobenzene
John Joseph Sudborough J. Chem. Soc. Trans. 1916 109 1339
3. The detection of organo-phosphorus pesticides on thin-layer chromatograms
P. J. Bunyan Analyst 1964 89 615
4. Preparation and properties of p-dimethylamino-N-thiosulphinylaniline
Derek H. R. Barton,Michael J. Robson J. Chem. Soc. Perkin Trans. 1 1974 1245
5. Aromatic azo-compounds. Part V. The absorption spectra of N-substituted 4-aminoazobenzenes and their mono-acid salts
G. M. Badger,R. G. Buttery,G. E. Lewis J. Chem. Soc. 1954 1888
6. Adsorption and micellisation of a surface-active dye in aqueous methanol solutions
Toyoko Imae,Chisako Mori,Shoichi Ikeda J. Chem. Soc. Faraday Trans. 1 1982 78 1359
7. 7. The reactivity of organophosphorus compounds. Part XIV. Deoxygenation of aromatic C-nitroso-compounds by triethyl phosphite and triphenylphosphine: a new cyclisation reaction
P. J. Bunyan,J. I. G. Cadogan J. Chem. Soc. 1963 42
8. 588. Isosbestic points
M. D. Cohen,E. Fischer J. Chem. Soc. 1962 3044
9. Index of subjects
J. Chem. Soc. Abstr. 1912 102 ii1381
10. Classical carbonium ions. Part 12. The deamination of 1- and 4-amino-n-octane
Richard M. Southam,Mark C. Whiting J. Chem. Soc. Perkin Trans. 2 1982 597

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