3-氨基-5-苯基吡唑
3-氨基-5-苯基吡唑结构式
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常用名 | 3-氨基-5-苯基吡唑 | 英文名 | 3-Phenyl-1H-pyrazol-5-amine |
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| CAS号 | 1572-10-7 | 分子量 | 159.19 | |
| 密度 | 1.2±0.1 g/cm3 | 沸点 | 442.3±33.0 °C at 760 mmHg | |
| 分子式 | C9H9N3 | 熔点 | 118-121ºC | |
| MSDS | 中文版 美版 | 闪点 | 251.5±12.6 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
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Anthranilamide-pyrazolo[1,5-a]pyrimidine conjugates as p53 activators in cervical cancer cells.
ChemMedChem 7(8) , 1453-64, (2012) A library of new anthranilamide-pyrazolo[1,5-a]pyrimidine conjugates were designed, synthesized, and evaluated for their anticancer activity in cervical cancer cells such as HeLa and SiHa that possess low levels of p53. All 24 conjugates showed antiproliferat... |
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Botulinum neurotoxin serotype A inhibitors: small-molecule mercaptoacetamide analogs.
Bioorg. Med. Chem. 17(8) , 3072-9, (2009) Botulinum neurotoxin elicits its paralytic activity through a zinc-dependant metalloprotease that cleaves proteins involved in neurotransmitter release. Currently, no drugs are available to reverse the effects of botulinum intoxication. Herein we report the d... |
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An efficient one-step synthesis of heterobiaryl pyrazolo[3,4-b]pyridines via indole ring opening.
Org. Lett. 11(22) , 5214-7, (2009) A mild one-step synthetic method to access privileged heterobiaryl pyrazolo[3,4-b]pyridines from indole-3-carboxaldehyde derivatives and a variety of aminopyrazoles has been developed. This novel method constructs heterobiaryls with the wide scope of substrat... |
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The conversion of isothiazoles into pyrazoles using hydrazine. Ioannidou HA and Koutentis PA
Tetrahedron 65(34) , 7023-7037, (2009)
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Crystal structure of chlorido-tris (3-amino-5-phenyl-1H pyrazole-N2) zinc (II) chloride, [ZnCl (C9H9N3)3] Cl. Jacimovic ZK, et al
Zeitsch. für Kristall. 226(3) , 397-399, (2011)
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Convenient synthesis of some new pyrazolo [5, 1-c] triazines, isoxazolo [3, 4-d] pyrimidine and pyridine derivatives containing benzofuran moiety. Abdelhamid AO, et al
Eur. J. Chem. 3(2) , 129-137, (2012)
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Syntheses of 3-pyrimidyl-and 3-pyranyl-5, 6-benzocoumarin derivatives. El-Deen IM, et al
Bull. Korean Chem. Soc. 23(4) , 610-612, (2002)
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Recent advances in the chemistry of ethoxycarbonyl isothiocyanate and related compounds. George B and Papadopoulos EP
J. Heterocycl. Chem. 20(5) , 1127-1142, (1983)
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