CAS: 2645-07-0; 2-(4-Nitrobenzamido)Acetic Acid
该化合物是一种硝基替代芳香化合物,其成分包括形式胺和碳酸性功能组,其结构特性使它在有机合成中成为有价值的中间体,特别是用于制备药品,农用化学品和特殊化学品.硝基乙酸组的存在增强了在电药和核生殖替代反应中的再活性,而碳箱酸混合物允许进一步衍生.该化合物经常用于浸泡混合反应和作为异环化合物的前体.其定义明确的晶体形式确保了一致性和稳定性,使之适合于需要精确化学转化的研究和工业应用.
- 英文名称2-(4-Nitrobenzamido)Acetic Acid
- 中文名称N-(4-硝基苯甲酰基)甘氨酸
- 其它别名Glycine,N-(p-nitrobenzoyl)- (8CI); Hippuric acid, p-nitro- (6CI,7CI); (4-Nitrobenzoylamino)acetic acid; 4-Nitrobenzoylglycine; 4-Nitrohippuric acid; N-(4-Nitrobenzoyl)glycine; N-(p-Nitrobenzoyl)glycine; p-Nitrohippuric acid
- CAS编号2645-07-0
- MFCD编号:MFCD00007349
- EINECS号:220-156-5
- FDA UNII编号:9HIU46T98M
- 分子式:C9H8N2O5分子量:224.17
- 产品CID: 1240018
- 产品分类有机原料→生命科学→氨基酸及其衍生物→甘氨酸及其衍生物
相似化合物
61-78-9 1219805-41-0 7512-77-8物理性质
MSDS等安全信息
上下游产品
ethyl 2-(4-nitrobenzamido)acetate 4-nitro-benzoyl chloride glycine H-oxazol-5-one2-(4-nitro-phenyl)-4H-oxazol-5-one p-Aminohippuric acid 4-nitro-N-(2-oxo-2-(phenylamino)ethyl)benzamide 2-(4-nitrophenyl)-4-(2-thienylmethylene)oxazol-5-one H-oxazol-5-one4-(2,6-dimethyl-pyran-4-ylidene)-2-(4-nitro-phenyl)-4H-oxazol-5-one合成工艺路线路线简述
📜2-<4-Nitrophenyl>-Oxazol-5-On置于hydroxide体系中,化学反应生成4-硝基马尿酸
参考文献:Structure-Reactivity Studies On The Equilibrium Reaction Between Phenolate Ions And 2-Aryloxazolin-5-Ones: Data Consistent With A Concerted Acyl-Group-Transfer Mechanism
标题:Structure-Reactivity Studies On The Equilibrium Reaction Between Phenolate Ions And 2-Aryloxazolin-5-Ones: Data Consistent With A Concerted Acyl-Group-Transfer Mechanism
摘要:
Doi:10.1021/ja00542A028
海关参考信息
- 2912110000-甲醛
2912120000-乙醛
2912210000-苯甲醛
2915110000-甲酸 - 💡 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-9217012-B2
优先权日:2009-04-08
标题 :Inhibitors of protein tyrosine phosphatases
发明人：ZHANG ZHONG-YIN; ZHANG SHENG
权利人:ZHANG ZHONG-YIN; ZHANG SHENG; UNIV INDIANA RES & TECH CORP
摘要:Disclosed herein are compounds that selectively inhibit members of the PTP family of enzymes. Synthesized compounds demonstrated selective inhibition of TC-PTP. Also provided are methods of using the compounds and formulations containing the compounds. Also described is a fluorescence-tagged combinatorial library synthesis and screening method. And methods of using these compounds to effect enzyme activity both in cells and in vitro as well as method of using these compounds to treat diseases in human and animals.
专利号:CN-118439966-A
优先权日:2024-07-05
标 题:Synthesis method of p-nitroaniline compound
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主要参考文献
[参考文献]: Luckose F, Et Al. Effects Of Amino Acid Derivatives On Physical, Mental, And Physiological Activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.合成参考文献
摘要:National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.
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