CAS: 603-45-2; Rosolic Acid, Indicator

该化合物是被归类为染色的有机化合物,具体而言,是一种亚索染色,其特点是其活跃的黄色至橙色,其特点是分子结构中存在阿索(-N=N-)功能组,Aurin在有机溶剂中可以溶解,水溶性有限,在包括纺织品和生物污点在内的各种应用中有用;该化合物在正常条件下具有稳定性,尽管在极端的pH或光暴露下可能会降解;Aurin还可能表现出荧光,这增强了其在某些分析和成像技术中的效用;然而,与许多阿索染色剂一样,它可能对环境和健康造成危险,因为一些亚索化合物在降解时会释放致癌的胺;因此,处理Aurin需要适当的安全措施来减轻潜在危害.总的来说,Aurin在工业和研究环境中,特别是在化学和生物学领域,都是一个重要的化合物.

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CAS号144-62-7 草酸 | CAS号108-95-2 苯酚 | CAS号456-55-3 三氟甲氧基苯 | CAS号56-23-5 四氯化碳 | CAS号64-18-6 甲酸 | CAS号76-06-2 氯化苦 | CAS号32858-93-8 2-(三氟甲氧基)苯酚 | CAS号95-57-8 邻氯苯酚 | CAS号450-96-4 1-氯-2-(三氟甲氧基)苯 | CAS号106-44-5 对甲酚 | CAS号53153-46-1 3,3,5-trimethyl... | CAS号603-44-1 4,4’,4’’-亚甲基三苯酚 | CAS号611-99-4 4,4'-二羟基二苯甲酮 | CAS号108-95-2 苯酚 | CAS号106-51-4 苯醌 | CAS号609-23-4 2,4,6三碘苯酚 | CAS号548-61-8 4,4',4''-三氨基三苯甲烷 | CAS号467-62-9 付玫瑰苯胺

合成工艺路线路线简述

  • 合成目标产物 Rosolic Acid 主要起始原料 Carbon Tetrachloride And Phenol
  • (文献来源)合成步骤主要原料 Carbon Tetrachloride 和 Phenol
📜三氟甲氧基苯置于氢氟酸,五氯化钽体系中,化学反应 4.0H,以25%的收率获得产物玫红酸
参考文献:Lability Of The Trifluoromethyl Group Of Trifluoromethoxybenzenes Under Hf/lewis Acid Conditions
标题:Lability Of The Trifluoromethyl Group Of Trifluoromethoxybenzenes Under Hf/lewis Acid Conditions
摘要:The Trifluoromethyl Functionality Of Trifluoromethoxybenzenes (Trifluoromethyl Phenyl Ethers) Becomes Labile Under Hf/lewis Acid Conditions. Substrates With An Unsubstituted Para-Position Shed Their-Cf(3) Groups While Performing A Friedel-Crafts Reaction Upon Another Substrate Molecule'S Trifluoromethoxy Group To Generate P-Rosolic Acids. Substrates That Had Blocking Groups At The Para-Positions Reacted Ortho. The Electron Donating Substituents Methoxy And Phenoxy Interfered With The Formation Of Rosolic Acids. (C) 2010 Elsevier B.V. All Rights Reserved.
DOI:10.1016/j.Jfluchem.2010.08.003

海关参考信息

专利信息


专利号:US-7355036-B2
优先权日:2001-07-03
标 题 :Two-stage protective groups for the synthesis of biopolymers
发明人:GUEIMIL RAMON; SCHEFFLER MATTHIAS; STAEHLER PEER F; BEIJER BARBRO
权利人:FEBIT AG
摘要:The invention relates to a method for the synthesis of a nucleic acid by gradual breakdown from protected synthesis building blocks carrying two-stage protective groups. The two-stage protective groups are split by means of a first exposure step and a subsequent chemical treatment step

专利号:US-7541165-B2
优先权日:2001-10-30
标 题 :Molecular detection systems utilizing reiterative oligonucleotide synthesis
发明人:HANNA MICHELLE M
权利人:RIBOMED BIOTECHNOLOGIES INC
摘要:The present invention provides methods for detecting the presence of a target molecule by generating multiple detectable oligonucleotides through reiterative enzymatic oligonucleotide synthesis events on a defined polynucleotide sequence. The methods generally comprise using a nucleoside, a mononucleotide, an oligonucleotide, or a polynucleotide, or analog thereof, to initiate synthesis of an oligonucleotide product that is substantially complementary to a target site on the defined polynucleotide sequence; optionally using nucleotides or nucleotide analogs as oligonucleotide chain elongators; using a chain terminator to terminate the polymerization reaction; and detecting multiple oligonucleotide products that have been synthesized by the polymerase. In one aspect, the invention provides a method for detecting a target protein, DNA or RNA by generating multiple detectable RNA oligoribonucleotides by abortive transcription.

专利号:US-11851651-B2
优先权日:2017-06-19
标 题 :Automated methods for scalable, parallelized enzymatic biopolymer synthesis and modification using microfluidic devices
发明人:BANAL JAMES; BERLEANT JOSEPH DON; SHEPHERD TYSON; BATHE MARK
权利人:MASSACHUSETTS INST TECHNOLOGY
摘要:Methods for the automated template-free synthesis of user-defined sequence controlled biopolymers using microfluidic devices are described. The methods facilitate simultaneous synthesis of up to thousands of uniquely addressed biopolymers from the controlled movement and combination of regents as fluid droplets using microfluidic and EWOD-based systems. In some forms, biopolymers including nucleic acids, peptides, carbohydrates, and lipids are synthesized from step-wise assembly of building blocks based on a user-defined sequence of droplet movements. In some forms, the methods synthesize uniquely addressed nucleic acids of up to 1,000 nucleotides in length. Methods for adding, removing and changing barcodes on biopolymers are also provided. Biopolymers synthesized according to the methods, and libraries and databases thereof are also described. Modified biopolymers, including chemically modified nucleotides and biopolymers conjugated to other molecules are described.

专利号:US-2004054162-A1
优先权日:2001-10-30
标 题:Molecular detection systems utilizing reiterative oligonucleotide synthesis
发明人:HANNA MICHELLE M
摘要:The present invention provides methods for detecting the presence of a target molecule by the use of nucleotide analogs containing moieties that enable detection. Such analogs may be incorporated into nucleic acids. In one embodiment, nucleotide analogs are used in a process generating multiple detectable oligonucleotides through reiterative enzymatic oligonucleotide synthesis events on a defined polynucleotide sequence. The methods generally comprise using a nucleoside, a mononucleotide, an oligonucleotide, or a polynucleotide, or analog thereof, to initiate synthesis of an oligonucleotide product that is substantially complementary to a target site on the defined polynucleotide sequence; optionally using nucleotides or nucleotide analogs as oligonucleotide chain elongators or chain terminators to terminate the polymerization reaction; and detecting multiple oligonucleotide products that have been synthesized by the polymerase.

专利号:US-2022233673-A1
优先权日:2019-06-04
标 题:METHODS OF PRODUCING SHIGA TOXIN B-SUBUNIT (STxB) MONOMERS AND OLIGOMERS, AND USES THEREOF
发明人:BILLET ANNE; SCHMIDT FRÉDÉRIC; JOHANNES LUDGER; SERVENT DENIS; MOURIER GILLES; TARTOUR ÉRIC; KAY MICHAEL; FULCHER JAMES M
权利人:INST CURIE; CENTRE NAT RECH SCIENT; INST NAT SANTE RECH MED; COMMISSARIAT A LENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES CEA; APHP ASSIST PUBLIQUE HOPITAUX DE PARIS; UNIV PARIS; UNIV OF UTAH RESEARCH FOUDATION; UNIV UTAH RES FOUND
摘要:A method of producing a monomer of a Shiga toxin B-subunit (STxB) protein or of a variant thereof by peptide chemical synthesis, as well as to a method of producing a pentamer of the STxB protein or of the variant thereof. The methods are particularly advantageous as they overcome major issues typically observed in peptide chemical synthesis, including solubility and purity issues.

专利号:US-7135565-B2
优先权日:2000-07-28
标题 :Synthesis of polynucleotides using combined oxidation/deprotection chemistry
发明人:DELLINGER DOUGLAS J; PERBOST MICHAEL G M; CARUTHERS MARVIN H; BETLEY JASON R
权利人:UNIV COLORADO
摘要:A method of synthesizing a polynucleotide which can, for example, be used during fabrication of an array. A second nucleoside is coupled to a first nucleoside through a phosphite linkage, with the second nucleoside having a hydroxyl protecting group that is a non-carbonate protecting group. The product of the foregoing step is exposed to a composition which both oxidizes the formed phosphite to a phosphate and deprotects the protected hydroxyl of the coupled nucleoside. The method has particular application to fabricating an addressable array of polynucleotides on a substrate which carries substrate bound moieties each with a hydroxyl group.

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1: Gao J, Cui JZ, Wang A, Chen HHR, Fong A, Matsubara JA. The reduction of XIAP is associated with inflammasome activation in RPE: implications for AMD pathogenesis. J Neuroinflammation. 2019 Aug 22;16(1):171. doi: 10.1186/s12974-019-1558-5.
2: Wang M, Hua Y, Keep RF, Wan S, Novakovic N, Xi G. Complement Inhibition Attenuates Early Erythrolysis in the Hematoma and Brain Injury in Aged Rats. Stroke. 2019 Jul;50(7):1859-1868. doi: 10.1161/STROKEAHA.119.025170. Epub 2019 Jun 10.
3: Verma P, Doharey PK, Yadav S, Omer A, Singh P, Saxena JK. Molecular cloning and characterization of protein disulfide isomerase of Brugia malayi, a human lymphatic filarial parasite. EXCLI J. 2017 Jun 1;16:824-839. doi: 10.17179/excli2017-214.

合成参考文献


摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
摘要:T. H. Lin, J. Chinese Chem. Soc. (Taiwan) 9, 220 (1962); CA 60, 7509b.
参考文献:10.1021/jm050617x
摘要:Sharma RK, Chopra S, Sharma SD, Pande V, Ramos MJ, Meguro K, Inoue J, Otsuka M. Biological evaluation, chelation, and molecular modeling studies of novel metal-chelating inhibitors of NF-kappaB-DNA binding: structure activity relationships. J Med Chem. 2006 Jun 15;49(12):3595–601. doi: 10.1021/jm050617x.
参考文献:10.1016/0006-291x(86)90877-6
摘要:Balzarini J, Mitsuya H, De Clercq E, Broder S. Aurintricarboxylic acid and evans blue represent two different classes of anionic compounds which selectively inhibit the cytopathogenicity of human T-cell lymphotropic virus type III/lymphadenopathy-associated virus. Biochemical and Biophysical Research Communications. 1986 Apr;136(1):64–71. doi: 10.1016/0006-291x(86)90877-6.
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