265-03-2 ((3H-1,5-Benzodiazepine)

快速询单

结构式：

3H-1,5-BenzodiazepineMOL文件

CAS号：

265-03-2

英文名称：

3H-1,5-Benzodiazepine

分子式：

C₉H₈N₂

分子量：

144.173221588135

3H-1,5-Benzodiazepine(265-03-2)名称与标识符

名称

英文别名：

3H-1,5-Benzodiazepine;

标识符

InChIKey：

UEGQYNDBLSUUET-UHFFFAOYSA-N

Inchi：

1S/C9H8N2/c1-2-5-9-8(4-1)10-6-3-7-11-9/h1-2,4-7H,3H2

SMILES：

N1C2=CC=CC=C2N=CCC=1

3H-1,5-Benzodiazepine(265-03-2)相关文献

1. 1,3-Dipolar cycloaddition of nitrilimines to 2,4-disubstituted-3H-1,5-benzodiazepines: remarkable effect of C4-substituent on diastereoselectivity
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3. 692. Diazepines. Part III. Some benzodiazepines
Douglas Lloyd,Ronald H. McDougall,Donald R. Marshall J. Chem. Soc. 1965 3785
4. Regioselective “hydroamination” of alk-3-ynones with non-symmetrical o-phenylenediamines. Synthesis of diversely substituted 3H-1,5-benzodiazepines via (Z)-3-amino-2-alkenones
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5. 1H nuclear magnetic resonance study of the association between 1,5-dialkyl-1,5-dihydro-1,5-benzodiazepine-2,4-diones and the shift reagent Eu(fod)3
Maria C. Aversa,Placido Giannetto,Antonino Saija J. Chem. Soc. Perkin Trans. 2 1987 1071
6. Reactions of 1,2-diaminobenzene with 1,3-diketones
Siegfried E. Drewes,Ursula J. Upfold J. Chem. Soc. Perkin Trans. 1 1977 1901
7. Electron-donating curved π-electronic systems that complex with buckyballs
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8. 76. The removal of toluene-p-sulphonyl groups from sulphonamides. Part I. Synthesis of Schiff bases
W. Paterson,G. R. Proctor J. Chem. Soc. 1965 485
9. Alkynylcarbenium ions and related unsaturated cations
Sergey M. Luk'yanov,Alla V. Koblik,Lyudmila A. Murad'yan Russ. Chem. Rev. 1998 67 817

265-03-2 ((3H-1,5-Benzodiazepine)

3H-1,5-Benzodiazepine(265-03-2)名称与标识符

名称

标识符

3H-1,5-Benzodiazepine(265-03-2)相关文献

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