CAS: 471-46-5; Oxamide

该化合物是一个有机化合物,其特征为氨化功能组;它是一种在水中溶解的白色晶状固体,其熔点相对较高;它以稳定性和低毒性著称,因此适合化学工业的各种应用;它的结构由两个与核心碳原子相连的碳原子组成,有助于形成氢结,提高极地溶剂中的溶解性;Oxamide经常被用作有机合成的试剂,可以作为生产其他含氮化合物的前体;此外,它由于它的热稳定性,有可能在农业中用作化肥和塑料及树脂的配制;总的来说,氧化胺是一种多用途化合物,在研究和工业方面都具有重大效用.

结构式图片

相似化合物

3551-78-8 333-18-6 5700-49-2

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号553-90-2 草酸二甲酯 | CAS号67-56-1 甲醇 | CAS号201230-82-2 carbon monoxide | CAS号79-40-3 二硫代草酰氨 | CAS号471-47-6 草氨酸 | CAS号543-27-1 氯甲酸异丁酯 | CAS号51802-55-2 5,7-dimethyl-6H... | CAS号148705-17-3 diisopropenyl o... | CAS号120-20-7 3,4-二甲氧基苯乙胺 | CAS号471-47-6 草氨酸 | CAS号55-21-0 苯甲酰胺 | CAS号463-58-1 羰基硫 | CAS号60-35-5 乙酰胺 | CAS号141-43-5 2-氨基乙醇 | CAS号107-21-1 乙二醇 | CAS号107-15-3 乙二胺 | CAS号620-81-5 草酰苯胺 | CAS号10543-64-3 N'-phenyloxamide | CAS号3030-75-9 Ethanedioic aci...

合成工艺路线路线简述

  • 合成目标产物 Oxamide 主要起始原料 Dimethyl Oxalate And Methanol
  • (文献来源)合成步骤主要原料 Dimethyl Oxalate 和 Methanol
氰置于h2So4,Acetic Acid体系中,用0%的收率获得产物草酰胺
参考文献:Gmelin Handbuch Der Anorganischen Chemie,Gmelin Handbook: C: Mvol.D1,4.10.9,Page 85-91
标题:Gmelin Handbuch Der Anorganischen Chemie,Gmelin Handbook: C: Mvol.D1,4.10.9,Page 85-91

海关参考信息

专利信息


专利号:US-5723619-A
优先权日:1997-01-13
标 题 :Method for the synthesis of deoxypyridinoline
发明人:HATCH ROBERT P
权利人:BAYER AG
摘要:Disclosed is a method for the chemical synthesis of deoxypyridinoline (DPD). The synthesis involves the preparation of a protected 3-hydroxypyridinium starting with a Nα-protected lysine and a 5,6-epoxy-2-N-protected-O-protected-(2S)-2-aminohexanoate with subsequent deprotection to provide the desired DPD.

专利号:US-12234200-B2
优先权日:2019-04-16
标 题:Synthetic methods of preparing esketamine
发明人:CHEN CHENG YI
权利人:JANSSEN PHARMACEUTICA NV
摘要:The present invention is directed to methods for the asymmetric synthesis of esketamine. The present invention is further directed to key intermediates in the asymmetric esketamine synthesis. In one embodiment, the invention is an asymmetric synthesis of esketamine comprising the conversion of (S)-2′-chloro-2-methoxy-3,4,5,6-5 tetrahydro-[1, 1′-biphenyl]-3-yl carbamate to (S)-2′-chloro-1-isocyanato-6-methoxy-1,2,3,4-tetrahydro-1,1′-biphenyl.

专利号:US-2009318592-A1
优先权日:2005-10-11
标 题 :Process for the Synthesis of Amine Ethers
发明人:FREY MARKUS; BROENNIMANN VALERIE
权利人:CIBA GEIGY CORP
摘要:The present invention relates to novel processes for the preparation of a sterically hindered amine ether by reacting a corresponding sterically hindered amine oxide with a ketone or an aldehyde with at least one reactive H in the presence of a peroxydisulphate. Products obtained by this process may be hydrogenated. The compounds made by these processes are particularly effective in the stabilization of polymer compositions against harmful effects of light, oxygen and/or heat and as flame-retardants for polymers.

专利号:US-6153777-A
优先权日:1999-11-02
标 题 :Synthesis of ansa-metallocene catalysts
发明人:JORDAN RICHARD F; ZHANG XINGWANG
权利人:UNIV IOWA RES FOUND
摘要:A process of preparing in high yield racemic ansa-metallocene complexes by reacting a chelated bisamide group 4 metal complex with an ansa-bis-cyclopentodrenyl dianion reagent. The meso isomers are not detectable in the reaction product.

专利号:EP-1404682-B1
优先权日:2001-06-29
标题:Method of inhibiting ptp 1b and/or t-cell ptp and/or other ptpases with an asp residue at position 48
发明人:HANSEN THOMAS KRUSE; OLSEN OLE HVILSTED; PETERSEN ANDERS KLARSKOV; LAU JESPER; ANDERSEN HENRIK SUNE; MOLLER NIELS PETER HUNDAHL
权利人:NOVO NORDISK AS
摘要:This invention relates to oxalylamide inhibitors of Protein Tyrosine Phosphatase 1B (PTP1B) and/or T-cell Protein Tyrosine Phosphatase (TC-PTP) and/or Protein Tyrosine Phosphatases (PTPases) having an aspartic acid (Asp) in position 48 (PTP1B numbering, Chernoff et al., Proc. Natl. Acad. Sci. USA 87: 2735-2789 (1989)) and a method of inhibiting such PTPases by exposing the enzyme to inhibitor compounds of formula 1. This invention also relates to (I) the design and selection of inhibitors, which bind to the active site of PTP1B and/or TC-PTP and/or PTPases having an aspartic acid (Asp) in position 48 (II) the synthesis of said inhibitors, methods for their preparation and (III) to compositions comprising the inhibitor compounds.

专利号:US-2007191516-A1
优先权日:2004-03-15
标题 :Process for the synthesis of amine ethers
发明人:FREY MARKUS; RAST VALERIE; BRAIG ADALBERT; KRAMER ANDREAS
权利人:FREY MARKUS; RAST VALERIE; BRAIG ADALBERT; KRAMER ANDREAS
摘要:A process for the preparation of a sterically hindered amine ether which comprises reacting a corresponding sterically hindered aminoxide with a C 5 -C 18 alk-1-ene in the presence of an organic hydroperoxide and optionally hydrogenating the resulting product as well as the product mixtures obtained therewith and their use as stabilizers and flame retardants.
成都博瑞特化学技术有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.aikeshiji.com
企业联系电话:4008-755-333👤
📞成都博瑞特化学技术有限公司 ⚠️参考联系方式
联系人:曹先生
电话:4008-755-333
手机:18080918076
传真:QQ: 800078821
邮箱:1312936220@qq.com
通信地址: 成都市锦江区静宁路9号
邮编: 610000
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:成都市锦江区静宁路9号
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
第 1 / 1 页
现货

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

✅ COA系统入驻 | 共享模式

主要参考文献

[参考文献]: Dodheri Syed Samiulla, Et Al. Discovery Of Indole Tetrafluorophenoxymethylketone-Based Potent Novel Small Molecule Inhibitors Of Caspase-3. Org Med Chem Lett. 2012 Jul 16;2(1):27.
[参考文献]: L Yang, Et Al. The Determination Of Oxalic Acid, Oxamic Acid, And Oxamide In A Drug Substance By Ion-Exclusion Chromatography. J Pharm Biomed Anal. 2000 Apr;22(3):487-93.
[参考文献]: Magdy Mohamed Hemdan, Et Al. Uses Of 1-(3-Cyano-4,5,6,7-Tetrahydrobenzo[参考文献]: Sergey P Gavrish, Et Al. Crystal And Molecular Structures Of Related Nickel(Ii) Complexes Of Open-Chain And Macrocyclic Oxamide-Based Ligands And The Peculiarities Of Water Aggregates In Their Crystal Lattices. Dalton Trans. 2007 Nov 7:(41):4708-14.
[参考文献]: Thanasis Gimisis, Et Al. Synthesis Of N-Glucopyranosidic Derivatives As Potential Inhibitors That Bind At The Catalytic Site Of Glycogen Phosphorylase. Mini Rev Med Chem. 2010 Oct;10(12):1127-38.

合成参考文献


参考文献:10.1107/s1600536811010294
摘要:Zhang W, Wang F, Zhang G, Xiao X. A triclinic polymorph withZ= 3 ofN,N′-bis(2-pyridyl)oxamide. Acta Crystallogr E Struct Rep Online. 2011 Mar 26;67(4):o972–3. doi: 10.1107/s1600536811010294.
参考文献:10.1107/s1600536811014978
摘要:Sun Y, Xu X. Bis{μ3-cis-N-(2-carboxylato-5-chlorophenyl)-N′-[3-(dimethylamino)propyl]oxamidato(3−)}bis(perchlorato-κO)bis(N,N,N′,N′-tetramethylethylenediamine)tetracopper(II). Acta Crystallogr E Struct Rep Online. 2011 Apr 29;67(5):m645–6. doi: 10.1107/s1600536811014978.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知