✦ LIBER ✦

Structure of p-(p-nitroanilino)phenyl isothiocyanate, C13H9N3O2S

✍ Scribed by Hardgrove Jnr, G. L. ;Einstein, J. R. ;Wei, C. H.

Book ID: 114501437
Publisher: International Union of Crystallography
Year: 1983
Tongue: English
Weight: 569 KB
Volume: 39
Category: Article
ISSN: 0108-2701
DOI: 10.1107/s0108270183005673

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Structure of 3-(p-ethoxyphenyl)sydnone (

Structure of 3-(p-ethoxyphenyl)sydnone (1), C10H10N2O3, and 3-(p-tolyl)sydnone (2), C9H8N2O2

✍ Wang, Y. ;Lee, P. L. ;Yeh, M. H. 📂 Article 📅 1984 🏛 International Union of Crystallography 🌐 English ⚖ 301 KB

Structure of 2-(p-bromophenoxy)-N-ethyl-

Structure of 2-(p-bromophenoxy)-N-ethyl-2-phenyl-N-(p-tolyl)ethanesulfonamide, C23H24BrNO3S

✍ Sekido, K. ;Yokomori, Y. ;Hirokawa, S. ;Okuma, K. ;Ohta, H. 📂 Article 📅 1985 🏛 International Union of Crystallography 🌐 English ⚖ 293 KB

Structure of guanidinomethylphosphonic a

Structure of guanidinomethylphosphonic acid monohydrate, C2H8N3O3P.H2O

✍ Sawka-Dobrowolska, W. ;Głowiak, T. ;Tyka, R. 📂 Article 📅 1984 🏛 International Union of Crystallography 🌐 English ⚖ 306 KB

Crystal structure of a new organic conde

Crystal structure of a new organic condensed phosphate (C6H9N3O)H2P2O7

✍ Noura Jouini; Latifa BenHamada; Amor Jouini 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 581 KB

Structure of N,N-bis(p-nitrophenylsulfon

Structure of N,N-bis(p-nitrophenylsulfonyl)phenethylamine, C20H17N3O8S2

✍ Curtis, V. A. ;Pavkovic, S. F. 📂 Article 📅 1983 🏛 International Union of Crystallography 🌐 English ⚖ 222 KB

13C chemical shifts and 1H-13C coupling

13C chemical shifts and 1H-13C coupling constants of N-phenyl-, N-p-fluorophenyl- and N-o-nitrophenylpyrazoles

✍ Mikael Begtrup; Per Vedsø; Pilar Cabildo; Rosa Maria Claramunt; Jose Elguero; Wi 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 264 KB

## Abstract The ^13^C chemical shifts and some ^1^H^13^C coupling constants of twelve __N__‐arylpyrazoles are reported. The assignments were made by using the effects of a fluorine substituent and two‐dimensional techniques.