CAS: 27511-99-5; Eterobarbital

英文名称Eterobarbital
中文名称依特比妥
其它别名Barbituricacid, 5-ethyl-1,3-bis(methoxymethyl)-5-phenyl- (8CI); 1,3-Bis(methoxymethyl)-5-ethyl-5-phenylbarbituricacid; 1,3-Bis(methoxymethyl)phenobarbital; Antilon; Eterobarb; Eterobarbital; N,N'-Bis(methoxymethyl)phenobarbital; N,N'-Dimethoxymethylphenobarbital
CAS编号27511-99-5
FDA UNII编号:432SI047GA
分子式:C16H20N2O5分子量:320.34
产品CID: 1255138
产品分类有机原料 → 有机杂环化合物 → 二嗪类

相似结构搜索
InChIKey: DACOQFZGGLCXMA-UHFFFAOYSA-N
1S/C16H20N2O5/c1-4-16(12-8-6-5-7-9-12)13(19)17(10-22-2)15(21)18(11-23-3)14(16)20/h5-9H,4,10-11H2,1-3H3
计算化学: 氢键受体数5.0氢键供体数0.0可旋转键数6.0

MSDS等安全信息

警示词Warning

上下游产品

苯巴比妥 Phenobarbital 50-06-6

合成工艺路线路线简述

📜苯巴比妥以62的收率获得甲醚巴比妥
参考文献:J. Med. Chem. 1971,14,187-189
标题:J. Med. Chem. 1971,14,187-189

海关参考信息

2902600000-乙苯
2902700000-异丙基苯
2912110000-甲醛
2912120000-乙醛
💡 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-2008214827-A1
优先权日:2004-02-03
标题:Synthesis of Cyanoimino-Benzoimidazoles
发明人：GOEHRING R RICHARD; WHITEHEAD JOHN; SHAO BIN
权利人:EURO CELTIQUE SA
摘要:Disclosed in certain embodiments is a process for synthesizing a compound of formula (V) and salts thereof.

专利号:CA-2555219-A1
优先权日:2004-02-03
标题 :Synthesis of cyanoimino-benzoimidazoles

专利号:WO-2005075459-A1
优先权日:2004-02-03
标题:Synthesis of cyanoimino-benzoimidazoles

专利号:EP-1711484-A4
优先权日:2004-02-03
标题:SYNTHESIS OF CYANOIMINO-BENZOIMIDAZOLES

专利号:EP-1711484-A1
优先权日:2004-02-03
标题:Synthesis of cyanoimino-benzoimidazoles

专利号:US-2014315720-A1
优先权日:2012-10-24
标题 :Polysaccharide ester microspheres and methods and articles relating thereto
发明人：FALLON DENIS G; GARRETT THOMAS S; KIZER LAWTON E; ZAZZARA KAREN L; COMBS MICHAEL T; JOHNSON RICHARD K; DEHART GARY
权利人:CELANESE ACETATE LLC
摘要:A method for producing a polysaccharide ester microsphere may include forming a polysaccharide ester product from a polysaccharide synthesis, wherein the polysaccharide ester product comprises a polysaccharide ester and a solvent; diluting the polysaccharide ester product, thereby yielding a polysaccharide ester dope; and forming a plurality of polysaccharide ester microspheres from the polysaccharide ester dope. Suitable polysaccharides may include, but are not limited to, starch, cellulose, hemicellulose, algenates, chitosan, and any combination thereof. Esters thereof may be organic esters (e.g., acetate and the like), inorganic esters (e.g., sulfonates and the like), or combinations thereof. Further, the solids conent of the polysaccharide ester dope, in some instances, may be greater than about 16 wt %.