CAS: 2580-79-2; Diaminoglyoxime
该化合物是一个有机化合物,其独特的结构特征为两个氨基组和两个氧化体功能组,通常由公式C2H6N2O2代表.该化合物是一种白色晶状固体,可在水中溶解,具有一系列有趣的化学特性.已知二氨基晶体与各种金属离子形成协调复合体的能力,使其在分析化学中有用,并成为潜在的离子体.此外,由于存在反应性功能组,它可以参与各种化学反应,包括氧化和凝聚反应.该化合物在有机合成领域也感兴趣,并可能在制药和材料科学中发挥作用.然而,由于潜在的毒性和再活性,在处理该化合物时,应当采取安全防范措施,正如许多有机化合物一样.
- 英文名称Diaminoglyoxime
- 中文名称二氨基乙二醛肟
- IUPAC名称N1,N2-dihydroxyoxalimidamide
- 其它别名Oxalamide Dioxime; Diaminoglyoxim; Diaminoglyoxime; 2,6-Dibromo-4-Tolylhydrazine Hydrochloride; N,N-Dihydroxyoxalamidine; 1,2-Diamino-1,2-Ethanedione Dioxime; N,N''-Dihydroxyethanediimidamide; Oxamide Dioxime
- CAS编号2580-79-2
- MFCD编号:MFCD00511299
- 分子式:C2H6N4O2分子量:118.1
- 产品CID: 1223738
- 产品分类有机原料→分子砌块→脂肪链类化合物
相似化合物
88741-11-1物理性质
MSDS等安全信息
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📜氰置于羟胺体系中,化学反应生成二氨基乙二醛肟
参考文献:二氨基乙二肟肟分析†
标题:二氨基乙二肟肟分析†
摘要:对二氨基乙二肟(dag)的制备和分析性质进行了研究.
Doi:10.1002/hlca.19570400531
海关参考信息
- 2921211000-乙二胺
- 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:US-2024043406-A1
优先权日:2020-12-18
标题 :Method for sequential one-pot synthesis of tkx-50
发明人：DELAGE ARTHUR; ECK GENEVIÈVE; ALAIME THIBAUD; LACEMON FRÉDÉRICK; KLAPOTKE THOMAS; STIERSTORFER JORG; BOLTER MARC
权利人:EURENCO FRANCE
摘要:The present invention relates to a sequential one-pot synthesis of TKX-50, suitable for larger-scale production, during which an acetyl halide is used during the cyclization of diazidoglyoxime so as to obtain 1,1′-diacetyl-5,5′-bistetrazole, which is then hydrolyzed to 5,5′-bistetrazole-1,1′-diolate, to which compound a hydroxylammonium salt is subsequently added.
专利号:EP-4263527-A1
优先权日:2020-12-18
标题 :Method for sequential one-pot synthesis of tkx-50
专利号:WO-2022129724-A1
优先权日:2020-12-18
标 题:Method for sequential one-pot synthesis of tkx-50
专利号:FR-3118034-A1
优先权日:2020-12-18
标题 :Process for the sequential one-pot ('one-pot') synthesis of TKX-50
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
主要参考文献
参考标题:Solid-Phase Versus Solution Synthesis Of Asymmetrically Disubstituted Furazano[3,4-B]Pyrazines作者:E. Fernández,S. Garcı́a-Ochoa,S. Huss,A. Mallo,J.M. Bueno,F. Micheli,A. Paio,E. Piga,P. Zarantonello |发布日期:2002.7
摘要:Herein We Describe A Straightforward Solid-Phase Synthesis Directed Towards The Preparation Of Families Of Asymmetrically Disubstituted Furazano[3,4-B]Pyrazines By Stepwise Displacement Of The Two Chlorine Atoms In 5,6-Dichlorofurazano[3,4-B]Pyrazine By Nucleophiles. This Synthesis Has Avoided Selectivity Problems Found In Solution Chemistry.
合成参考文献
摘要:H. E. Ungnade, L. W. Kissinger, A. Narath and D. C. Barham, J. Org. Chem. 28, 134 (1963).
摘要:P. E. Wenger, O. Monnier and I. Kapetanidis, Helv. Chim. Acta 40, 1456 (1957).
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