CAS: 74243-85-9; Diethyl (2R,3R)-Oxirane-2,3-Dicarboxylate

该化合物是一种有机化合物,其特点是氧气(过氧化物)结构,具有三环醚特征.该化合物含有两个碳酸甲酯酯酯组,有助于极地溶剂中的再活性和溶性.2R,3R)配置表明在手工业中心有特定的立体化学,可影响其生物活动和相互作用.二乙基(2R,3R)-毒气-2,3-dicaboxylate通常对浅黄色液体无色,表现出一种舒适的气味.它被用于有机合成,特别是用于制作各种药品和农用化学品,因为它能够进行环开反应和形成多种衍生物.该化合物还具有材料科学的兴趣,有助于其在聚合物化学中的潜在应用.应当参考安全数据,因为它可能构成反应性有机化合物的典型危害,包括易燃性和接触时潜在的健康风险.

结构式图片

相似化合物

16533-72-5 141-36-6 17087-75-1

欧盟法规

ECHA物质C&L通报

上下游产品

2-Bromo-3-hydroxy-succinic acid diethyl ester diethyl Fumarate but-2-enedioic acid diethyl ester ethanoldiethylmalate DL-trans-epoxysuccinic acid ethyl (2S,3S)-3-carboxylate oxirane-2-carboxylic acid ethyl (2S,3S)-2,3-epoxysuccinate

合成工艺路线路线简述

  • 合成目标产物 Diethyl (2R,3R)-(-)-2,3-Epoxysuccinate 主要起始原料 Diethyl (2S,3S)-2-Bromo-3-Hydroxysuccinate
  • (文献来源)合成步骤主要原料 Diethyl (2S,3S)-2-Bromo-3-Hydroxysuccinate
📜L-(+)-酒石酸二乙酯置于氢溴酸,溶剂黄146,Sodium Ethanolate体系中,化学反应生成 (2R,3R)-二乙基-2,3-环氧琥珀酸
参考文献: Antibacterial Compounds And Methods For Treating Gram Positive Bacterial Infections[fr] Composes Antibacteriens Et Methodes De Traitement D'Infections Bacteriennes Gram Positif
标题: Antibacterial Compounds And Methods For Treating Gram Positive Bacterial Infections[fr] Composes Antibacteriens Et Methodes De Traitement D'Infections Bacteriennes Gram Positif

海关参考信息

专利信息


专利号:US-7393954-B2
优先权日:2002-12-12
标题:Process for the production of pentostatin aglycone and pentostatin
发明人:NADJI SOURENA; SMOOT JAMES; SAMPATH UMASHANKER
权利人:RELIABLE BIOPHARMACEUTICAL COR
摘要:A novel, scaleable and improved process for preparing pentostatin and its analogs is disclosed. The method comprises the diastereospecific synthesis of the nucleobase from commercially available L-Dialkyl tartarates.

专利号:US-4794108-A
优先权日:1984-04-24
标题:1-carboxymethoxy acetidinones and their production
发明人:KISHIMOTO SHOJI; SENDAI MICHIYUKI; OCHIAI MICHIHIKO
权利人:TAKEDA CHEMICAL INDUSTRIES LTD
摘要:A 2-azetidinone derivative having a group of the formula wherein R1 and R2 are the same or different and each represents a hydrogen atom, alkyl, aryl or arylalkyl which may have a substituent at the 1-position and an amino group, at the 3-position, which may be acylated or protected, its salt or ester, and methods of producing the same, (1) a method comprising subjecting a 2-azetidinone derivative having a group of the formula wherein the symbols are as defined above at the 1-position and an amino group at the 3-position, its salt or ester to an acylation or protective-group introduction reaction, and (2) a method comprising reacting a 2-azetidinone derivative having a hydroxy group at the 1-position and an amino group, at the 3-position, which may be acylated or protected, or its salt with a compound of the formula wherein W is a halogen atom; other symbols are as defined above, its salt or ester. The above objective compounds are utilizable as excellent antimicrobial agents or as valuable intermediates for the synthesis of the same.

专利号:EP-0135194-A1
优先权日:1983-09-16
标题:Azetidinones and their production
发明人:KISHIMOTO SHOJI; SENDAI MICHIYUKI; OCHIAI MICHIHIKO
权利人:TAKEDA CHEMICAL INDUSTRIES LTD
摘要:A 2-azetidinone derivative having a group of the formulan wherein R' and R 2 are the same or different and each represents a hydrogen atom, alkyl, aryl or arylalkyl which may have a substituent at the 1-position and an amino group, at the 3-position, which may be acylated or protected, its salts or ester, and methods of producing the same,n (1) a method comprising subjecting a 2-azetidinone derivative having a group of the formulan wherein the symbols are as defined above at the 1-position and an amino group at the 3-position, its salt or ester to an acylation or protective-group introduction reaction, and (2) a method comprising reacting a 2-azetidinone derivative having a hydroxy group at the 1-position and an amino group at the 3-position, which may be acylated or protected, or its salt with a compound of the formulan wherein W is a halogen atom; other symbols are as defined above, its salt or ester. The above objective compounds are utilizable as excellent antimicrobial agents or as valuable intermediates for the synthesis of the same.

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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

合成参考文献


摘要:Garbaccio, R. M.; Wolkenberg, S. E., Science of Synthesis, (2007) 20, 1150.
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