2,5-Thiophenedicarboxaldehyde
2,5-Thiophenedicarboxaldehyde structure
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Common Name | 2,5-Thiophenedicarboxaldehyde | ||
|---|---|---|---|---|
| CAS Number | 932-95-6 | Molecular Weight | 140.16000 | |
| Density | 1.37g/cm3 | Boiling Point | 302ºC at 760mmHg | |
| Molecular Formula | C6H4O2S | Melting Point | 114-117ºC | |
| MSDS | Chinese USA | Flash Point | 136.5ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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(Photo)physical Properties of New Molecular Glasses End-Capped with Thiophene Rings Composed of Diimide and Imine Units.
J. Phys. Chem. C Nanomater. Interfaces 118(24) , 13070-13086, (2014) New symmetrical arylene bisimide derivatives formed by using electron-donating-electron-accepting systems were synthesized. They consist of a phthalic diimide or naphthalenediimide core and imine linkages and are end-capped with thiophene, bithiophene, and (e... |
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Chiral Synthesis via Organoboranes. 46. An Efficient Preparation of Chiral Pyridino- and Thiopheno-18-crown-6 Ligands from Enantiomerically Pure C(2)-Symmetric Pyridine- and Thiophenediols(1).
J. Org. Chem. 64(3) , 721-725, (1999) Asymmetric reduction of 2,6-diacylpyridines with B-chlorodiisopinocampheylborane provides the corresponding C(2)-symmetric diols in very high de and ee. Asymmetric allylboration of 2,6-pyridinedicarboxaldehyde and 2,5-thiophenedicarboxaldehyde provides the co... |
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Structure-in vitro activity relationships of pentamidine analogues and dication-substituted bis-benzimidazoles as new antifungal agents.
Antimicrob. Agents Chemother. 42(10) , 2495-502, (1998) Twenty analogues of pentamidine, 7 primary metabolites of pentamidine, and 30 dicationic substituted bis-benzimidazoles were screened for their inhibitory and fungicidal activities against Candida albicans and Cryptococcus neoformans. A majority of the compou... |
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Tunable electroluminescence from silicon-containing poly (p-phenylenevinylene)-related copolymers with well-defined structures. Kim HK, et al.
Macromolecules 31(4) , 1114-23, (1998)
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The Preparation of 2, 5-Thiophenedicarboxaldehyde. Sone T.
Bull. Chem. Soc. Jpn. 37(8) , 1197-1200, (1964)
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