Prasad, Pragati K. et al. published their research in Organic Letters in 2016 | CAS: 40594-98-7

Ethyl 1H-1,2,3-triazole-5-carboxylate (cas: 40594-98-7) belongs to triazole derivatives. The triazole ring is a relatively stable functional group, and the triazole bond can be used for a variety of applications, such as replacing the phosphate backbone of DNA.Triazole heterocyclic structures are found to form many weak nonbond interactions with the receptors and enzymes in biological systems.Quality Control of Ethyl 1H-1,2,3-triazole-5-carboxylate

Regioselective Oxo-Amination of Alkenes and Enol Ethers with N-Bromosuccinimide-Dimethyl Sulfoxide Combination: A Facile Synthesis of α-Amino-Ketones and Esters was written by Prasad, Pragati K.;Reddi, Rambabu N.;Sudalai, Arumugam. And the article was included in Organic Letters in 2016.Quality Control of Ethyl 1H-1,2,3-triazole-5-carboxylate This article mentions the following:

An unprecedented conversion of alkenes and enol ethers to the corresponding α-imido carbonyl compounds with excellent regioselectivity and yields has been developed. This oxo-amination process employs readily available N-bromosuccinimide (NBS) and secondary amines as N-sources and DMSO (DMSO) as the oxidant and also leads to the production of amino alcs. in a single step on reduction, thus broadening the scope of this operationally simple reaction. For the first time, the formation of reactive Me2S+-O-Br species generated by the interaction of NBS with DMSO has been proven. In the experiment, the researchers used many compounds, for example, Ethyl 1H-1,2,3-triazole-5-carboxylate (cas: 40594-98-7Quality Control of Ethyl 1H-1,2,3-triazole-5-carboxylate).

Ethyl 1H-1,2,3-triazole-5-carboxylate (cas: 40594-98-7) belongs to triazole derivatives. The triazole ring is a relatively stable functional group, and the triazole bond can be used for a variety of applications, such as replacing the phosphate backbone of DNA.Triazole heterocyclic structures are found to form many weak nonbond interactions with the receptors and enzymes in biological systems.Quality Control of Ethyl 1H-1,2,3-triazole-5-carboxylate

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Sun, Rui et al. published their research in Dalton Transactions in 2017 | CAS: 4546-95-6

1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6) belongs to triazole derivatives. However, triazoles are also useful in bioorthogonal chemistry, because the large number of nitrogen atoms causes triazoles to react similar to azides. Both the triazoles and their derivatives have significant biological properties including antimicrobial, antiviral, antitubercular, anticancer, anticonvulsant, analgesic, antioxidant, anti-inflammatory, and antidepressant activities.COA of Formula: C4H3N3O4

Co-ligand tuned pyrimidine-2-carboxylate Mn(II) complexes from a 2D 63 layer to an interpenetrated srs-net was written by Sun, Rui;Gao, Su-Mei;Wang, Shao-Qiang;Song, Wei-Chao;Zhao, Jiong-Peng;Liu, Fu-Chen. And the article was included in Dalton Transactions in 2017.COA of Formula: C4H3N3O4 This article mentions the following:

A 63 2D layer complex [Mn3Cl3(L3)]n·H2O (1) (L = pyrimidine-2-carboxylate) was obtained by assembling 2-cyanopyrimidine and manganese chloride, in which the L ligands were generated in situ. In 1 six-membered Mn rings were constructed from MnII ions and L ligands, which were connected to each other by double chloride anions affording a 2D layer. When the chloride anions in 1 were substituted partly by formate, [Mn4Cl3L4(HCO2)]n (2) was obtained. In 2, the L ligands bridge MnII to give a 1D chain, which was further connected by the double chloride anions and Cl/formate bridges to form a two-fold interpenetrated srs-net. 2 Exhibits an obvious SHG response of ∼0.8 times that of KDP. Furthermore, 2 is an antiferromagnet with a field induced spin flop transition. In the experiment, the researchers used many compounds, for example, 1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6COA of Formula: C4H3N3O4).

1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6) belongs to triazole derivatives. However, triazoles are also useful in bioorthogonal chemistry, because the large number of nitrogen atoms causes triazoles to react similar to azides. Both the triazoles and their derivatives have significant biological properties including antimicrobial, antiviral, antitubercular, anticancer, anticonvulsant, analgesic, antioxidant, anti-inflammatory, and antidepressant activities.COA of Formula: C4H3N3O4

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Tian, Dan et al. published their research in CrystEngComm in 2013 | CAS: 4546-95-6

1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6) belongs to triazole derivatives. However, triazoles are also useful in bioorthogonal chemistry, because the large number of nitrogen atoms causes triazoles to react similar to azides. Triazoles are compounds with a vast spectrum of applications, varying from materials (polymers), agricultural chemicals, pharmaceuticals, photoactive chemicals and dyes.Product Details of 4546-95-6

Edge-directed assembly of a 3D 2p-3d heterometallic metal-organic framework based on a cubic Co8(TzDC)12 cage was written by Tian, Dan;Liu, Sui-Jun;Chang, Ze;Zhang, Ying-Hui;Zhao, Jiong-Peng;Bu, Xian-He. And the article was included in CrystEngComm in 2013.Product Details of 4546-95-6 This article mentions the following:

A three-dimensional (3D) heterometallic metal-organic framework containing cubic-like cages, {[Co3Na6(TzDC)4(H2O)6]·7H2O}n (1) (H3TzDC = 1,2,3-triazole-4,5-dicarboxylic acid), was synthesized by the edge-directed self-assembly of TzDC3-, Co2+ and Na+ ions. Crystal data reveals that one hydrous Co2+ cation is embedded in the central cavity of a cubic-like cage [Co8(TzDC)12]20- with eight Co2+ cations as the corners and twelve TzDC3- ligands as the edges. The cages are further bridged by Na+ ions to result in a 3-dimensional framework with pcu topol. Magnetic study indicates that besides the spin-orbit coupling of Co2+ ions, an antiferromagnetic exchange interaction was found to exist between the Co2+ ions in the Co9 cluster of 1. In the experiment, the researchers used many compounds, for example, 1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6Product Details of 4546-95-6).

1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6) belongs to triazole derivatives. However, triazoles are also useful in bioorthogonal chemistry, because the large number of nitrogen atoms causes triazoles to react similar to azides. Triazoles are compounds with a vast spectrum of applications, varying from materials (polymers), agricultural chemicals, pharmaceuticals, photoactive chemicals and dyes.Product Details of 4546-95-6

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Mondal, Palash et al. published their research in Journal of Physical Chemistry C in 2019 | CAS: 4546-95-6

1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6) belongs to triazole derivatives. The many free lone pairs in triazoles make them useful as coordination compounds, although not typically as haptic ligands. 1,2,3-Triazoles are usually prepared following (3+2) cycloaddition protocols. A common technique for unsubstituted triazoles is the Huisgen azide-alkyne 1,3-dipolar cycloaddition: a azide and an alkyne react at high temperature to form a ring. However, the Huisgen strategy produces a mixture of isomers (typically 1,4- and 1,5-disubstituted) when used to produce substituted triazoles.Product Details of 4546-95-6

Colorimetric Dual Sensors of Metal Ions Based on 1,2,3-Triazole-4,5-Dicarboxylic Acid-Functionalized Gold Nanoparticles was written by Mondal, Palash;Yarger, Jeffery L.. And the article was included in Journal of Physical Chemistry C in 2019.Product Details of 4546-95-6 This article mentions the following:

A simple, rapid, selective, and cost-effective colorimetric assay for Cr3+ and Eu3+ ion detection has been developed using functionalized gold nanoparticles. Gold nanoparticles (AuNPs) were prepared using HAuCl4, where sodium citrate is a reducing agent as well as a capping agent, and then functionalized with 1,2,3-triazole-4,5-dicarboxylic acid (TADA). Fourier transform IR (FTIR) and Raman spectroscopies suggested that TADA was functionalized on the surface of AuNPs through the N atom of triazole. The TADA-functionalized gold nanoparticles (TADA@AuNPs) simultaneously detect Cr3+ and Eu3+ ions from aqueous solution and showed different responses to the two metal ions (Cr3+ and Eu3+) based on an aggregation-induced color change of AuNPs. They showed a color change from wine red to blue, which was easily detected by the naked eye, as well as by UV-visible and FTIR spectroscopies. The surface plasmon resonance absorbances of Cr3+ and Eu3+ are 633 and 671 nm, resp., when Cr3+ and Eu3+ react with TADA@AuNPs and showed good linearity with Cr3+ and Eu3+ concentrations with detection limits 5.89 nM and 4.30 μM, resp. (S/N = 3). The TADA@AuNPs showed excellent selectivity toward Cr3+ and Eu3+ compared to those of the 16 different metal ions. We had also tested the selectivity of TADA@AuNPs toward Eu3+ compared to that of the other 10 lanthanide systems. Optimal detection was achieved toward Cr3+ and Eu3+ ions in the pH range 4-10. In addition, TADA@AuNPs were applied to detect Cr3+ and Eu3+ ions from lake water showing low interference. In the experiment, the researchers used many compounds, for example, 1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6Product Details of 4546-95-6).

1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6) belongs to triazole derivatives. The many free lone pairs in triazoles make them useful as coordination compounds, although not typically as haptic ligands. 1,2,3-Triazoles are usually prepared following (3+2) cycloaddition protocols. A common technique for unsubstituted triazoles is the Huisgen azide-alkyne 1,3-dipolar cycloaddition: a azide and an alkyne react at high temperature to form a ring. However, the Huisgen strategy produces a mixture of isomers (typically 1,4- and 1,5-disubstituted) when used to produce substituted triazoles.Product Details of 4546-95-6

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Wang, Lihua et al. published their research in Inorganic Chemistry Communications in 2015 | CAS: 157069-48-2

4-(4H-1,2,4-Triazol-4-yl)benzoic acid (cas: 157069-48-2) belongs to triazole derivatives. The triazole ring is a relatively stable functional group, and the triazole bond can be used for a variety of applications, such as replacing the phosphate backbone of DNA. Due to the structural characteristics, both 1,2,3- and 1,2,4-triazoles are able to accommodate a broad range of substituents (electrophiles and nucleophiles) around the core structures and pave the way for the construction of diverse novel bioactive molecules.Recommanded Product: 157069-48-2

A 3D-diamond-like metal-organic framework: Crystal structure, nonlinear optical effect and high thermal stability was written by Wang, Lihua;Ye, Yingxiang;Zhang, Liuqin;Chen, Qianhuo;Ma, Xiuling;Zhang, Zhangjing;Xiang, Shengchang. And the article was included in Inorganic Chemistry Communications in 2015.Recommanded Product: 157069-48-2 This article mentions the following:

A new metal-organic framework [Zn(cpt)(ATZ)]n (1, HATZ = 5-amino-1H-tetrazol, Hcpt = 4-(4H-1,2,4-Triazol-4-yl)benzoic acid), has been solvothermally synthesized and structurally characterized by single crystal X-ray diffraction. Structural anal. shows that compound 1 is a three-dimensional (3D) framework with 3-fold interpenetrated diamond topol. where the Zn(II) centers are all 4-coordinated. Compound 1 exhibits high thermal stability up to 370 °C, and weak second-order nonlinear optical coefficient as ca. 0.13 times as that of potassium dihydrogen phosphate (KDP), and also displays blue photoluminescence at room temperature In the experiment, the researchers used many compounds, for example, 4-(4H-1,2,4-Triazol-4-yl)benzoic acid (cas: 157069-48-2Recommanded Product: 157069-48-2).

4-(4H-1,2,4-Triazol-4-yl)benzoic acid (cas: 157069-48-2) belongs to triazole derivatives. The triazole ring is a relatively stable functional group, and the triazole bond can be used for a variety of applications, such as replacing the phosphate backbone of DNA. Due to the structural characteristics, both 1,2,3- and 1,2,4-triazoles are able to accommodate a broad range of substituents (electrophiles and nucleophiles) around the core structures and pave the way for the construction of diverse novel bioactive molecules.Recommanded Product: 157069-48-2

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics