CAS: 13280-60-9; 5-Amino-2-Nitrobenzoic Acid

该化合物是一种有机化合物,其特征是附于苯甲酸结构的氨基和硝基功能组,其分子式为C7H6N2O3,表明其含有7个碳原子,6个氢原子,2个氮原子和3个氧原子.该化合物一般是一种黄色晶状固体,由于它的碳盒酸和氨基化合物组,在水和酒精等极溶剂中溶解.硝基化合物有助于其再活性,使其在各种化学合成和应用中有用,包括作为染料生产和药物的中间体.氨基氨基氨基酸组的存在允许进一步衍生,加强其在有机合成中的效用.此外,5-氨基-2-硝基苯甲酸可以展示生物活动,这可能对药用化学有益.应当参考安全数据,因为许多硝基化合物都可能造成毒性或环境关切的危害.

结构式图片

相似化合物

35998-96-0 610-74-2 77376-03-5

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

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CAS号552-16-9 2-硝基苯甲酸 | CAS号1055310-21-8 2-nitro-5-((((4... | CAS号1055310-22-9 2-nitro-5-((((2... | CAS号1055310-23-0 2-nitro-5-((((3... | CAS号1055310-24-1 2-nitro-5-((((5... | CAS号52033-70-2 3-苯乙酰氨基-6-硝基苯甲酸 | CAS号4368-83-6 5-乙酰氨基-2-硝基苯甲酸 | CAS号20632-43-3 3-[(氨基羰基)氨基]苯甲酸 | CAS号50670-83-2 5-乙酰氨基邻氨基苯甲酸 | CAS号100-01-6 对硝基苯胺 | CAS号552-16-9 2-硝基苯甲酸 | CAS号106-50-3 对苯二胺 | CAS号610-74-2 2,5-二氨基苯甲酸 | CAS号610-37-7 5-羟基-2-硝基苯甲酸 | CAS号35674-28-3 2-硝基-5-碘苯甲酸 | CAS号35998-96-0 5-氨基-2-硝基-苯甲酸甲酯 | CAS号77376-03-5 (5-氨基-2-硝基苯基)甲醇 | CAS号89165-27-5 2-nitro-5-[(2,2...

合成工艺路线路线简述

    2-Nitro-5-[[4-[[4-[(2-Phenylacetyl)Amino]Phenyl]Methoxycarbonylamino]Phenyl]Methoxycarbonylamino]Benzoic Acid置于penicillin-G-Amidase体系中,化学反应生成5-氨基-2-硝基苯甲酸
    参考文献:消除氮杂醌的方法:生理条件下1,6-和1,4-消除的比较研究.
    标题:消除氮杂醌的方法:生理条件下1,6-和1,4-消除的比较研究.
    摘要:消除氮杂醌是一个强大而有效的反应,可用于拆解前药系统中的间隔基.我们和其他人已经使用间隔子技术来开发树突状和聚合的自消灭分子系统,这些系统可以在刺激事件发生时通过类似多米诺的机制进行分解.在本报告中,我们研究了可通过对位和邻位氮杂醌甲基化物消除而分解的系统的分解.用经历单个1,6-或1,4-消除的分子和经历双重1,6-和1,4-消除的分子评估拆卸.在生理条件下,1,6-消除比1,4-消除略快.这项研究揭示了前药系统的拆卸行为.
    Doi:10.1039/b808198K

    海关参考信息

    专利信息


    专利号:US-5115099-A
    优先权日:1988-06-14
    标 题:Substrates for determination of enzyme activity and intermediates for synthesis of the substrates as well as process for producing the intermediates
    发明人:KUROIWA KATSUMASA; MATSUURA HITOSHI; KATAYAMA KATSUHIRO; NAKATSUYAMA SHUICHI; NAGASAWA TAKESHI; ENDO KOJI
    权利人:NITTO BOSEKI CO LTD
    摘要:Novel compounds represented by the following formula: ##STR1## wherein A represents a specific amino acid residue are excellent as substrates for determination of enzyme activity such as trypsin, etc. The compounds can be synthesized from novel arginyl-3-tert-alkyloxycarbonyl-4-nitroanilides by a novel process comprising a selective deprotection step whereby the protecting group on the α-amine group of arginine is removed in the presence of a hydrochloric acid, acetic acid and dimethylformamide mixture, but a tert-alkyl protecting group on the --COOH group of the nitroanilide ring is not removed by this step.

    专利号:EP-3431490-B1
    优先权日:2017-07-17
    标 题:Chemical compounds for use as diagnostic markers of inflammation and neoplams, the method for synthesis of the chemical compounds, diagnostic kit for use in diagnosis of inflammatory processes and epithelial neoplasms and in vitro diagnostic method of inflammatory processes and epithelial neoplasms
    发明人:LESNER ADAM; GRUBA NATALIA
    权利人:UNIV GDANSKI

    专利号:EP-3431490-A1
    优先权日:2017-07-17
    标题 :Chemical compounds for use as diagnostic markers of inflammation and neoplams, the method for synthesis of the chemical compounds, diagnostic kit for use in diagnosis of inflammatory processes and epithelial neoplasms and in vitro diagnostic method of inflammatory processes and epithelial neoplasms

    专利号:WO-2025082311-A1
    优先权日:2023-10-16
    标题:Solid-phase simple synthesis method for peptidol
    发明人:KAO CHAI-LIN; CHEN HUI-TING; CHEN SZU-HSUAN
    权利人:UNIV KAOHSIUNG MEDICAL
    摘要:A 3,4-diaminobenzoic acid (Dbz) group on a resin is activated by means of isoamyl nitrite to form benzotriazole (Bt), and a reduction reaction is then performed by using sodium borohydride (NaBH4) as a reducing agent. A peptidol can be obtained by means of a rapid reaction and only a simple filtering method; and the generation of by-products accompanying with the reaction can be reduced by changing conditions.

    专利号:EP-0513863-A1
    优先权日:1988-06-14
    标题:Substrates for determination of enzyme activity and intermediates for synthesis of the substrates as well as process for producing the intermediates

    专利号:EP-0513863-B1
    优先权日:1988-06-14
    标题:Substrates for determination of enzyme activity and intermediates for synthesis of the substrates as well as process for producing the intermediates
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    主要参考文献

    参考标题:Design And Synthesis Of New Barbituric- And Thiobarbituric Acid Derivatives As Potent Urease Inhibitors: Structure Activity Relationship And Molecular Modeling Studies
    作者:Abdul Rauf,Sohail Shahzad,Marek Bajda,Muhammad Yar,Faiz Ahmed,Nazar Hussain,Muhammad Nadeem Akhtar,Ajmal Khan,Jakub Jończyk |发布日期:2015.9
    摘要:In This Study 36 New Compounds Were Synthesized By Condensing Barbituric Acid Or Thiobarbituric Acid And Respective Anilines (Bearing Different Substituents) In The Presence Of Triethyl Orthoformate In Good Yields. In Vitro Urease Inhibition Studies Against Jack Bean Urease Revealed That Barbituric Acid Derived Compounds (1-9 And 19-27) Were Found To Exhibit Low To Moderate Activity However Thiobarbituric

    合成参考文献


    参考文献:10.1016/j.bbrc.2004.04.170
    摘要:Zabłotna E, Dysasz H, Lesner A, Jaśkiewicz A, Kaźmierczak K, Miecznikowska H, Rolka K. A simple method for selection of trypsin chromogenic substrates using combinatorial chemistry approach. Biochemical and Biophysical Research Communications. 2004 Jun;319(1):185–8. doi: 10.1016/j.bbrc.2004.04.170.
    参考文献:10.1186/1472-6750-10-7
    摘要:Maresová H, Marková Z, Valesová R, Sklenár J, Kyslík P. Heterologous expression of leader-less pga gene in Pichia pastoris: intracellular production of prokaryotic enzyme. BMC Biotechnol. 2010 Feb 03;10():7.
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