Tag: 100-200

Wang, Liang; Zhu, Kai-qiang; Wu, Wen-ting; Chen, Qun; He, Ming-yang published an article in 2015, the title of the article was n-Bu4NI-catalyzed direct amination of ethers with aryl tetrazoles and triazoles via cross-dehydrogenative coupling reaction.HPLC of Formula: 5301-96-2 And the article contains the following content:

An efficient, metal-free protocol for direct amination of ethers with aryl tetrazoles and triazoles has been developed using tetrabutylammonium iodide (TBAI) as a catalyst and tert-Bu hydroperoxide (t-BuOOH) as an oxidant. A series of ethers, aryl tetrazoles as well as triazoles are tolerated in this system, giving the corresponding products in moderate to good yields. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).HPLC of Formula: 5301-96-2

The Article related to amination ether aryltetrazole aryltriazole cross dehydrogenative coupling, metal free amination tetrabutylammonium iodide catalyst tertbutyl hydroperoxide oxidant, Heterocyclic Compounds (More Than One Hetero Atom): General and other aspects.HPLC of Formula: 5301-96-2

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

On April 7, 1998, Bolkan, Steven A.; Dunn, Steve published a patent.Synthetic Route of 5301-96-2 The title of the patent was Aqueous metal cleaner having an anticorrosion system. And the patent contained the following:

The title composition is composed of an alk. metal salt, a surfactant, and a corrosion inhibitor with a pH ∼7.5 to <10, preferably silicate free, of a combination of a triazole compound and an alkali metal borate. The use of 1,2,3-benzotriazole (Cobratec) and borax prevent discoloration of steel in addition to providing an anticorrosive effect at mild pH levels. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Synthetic Route of 5301-96-2

The Article related to aqueous cleaning composition corrosion inhibitor, borate alkali triazole corrosion inhibitor, mild alk aqueous cleaner copper, Surface Active Agents and Detergents: Cleaning Compositions and other aspects.Synthetic Route of 5301-96-2

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

On May 3, 2019, Yang, Yong-Zheng; Song, Ren-Jie; Li, Jin-Heng published an article.HPLC of Formula: 5301-96-2 The title of the article was Intermolecular Anodic Oxidative Cross-Dehydrogenative C(sp3)-N Bond-Coupling Reactions of Xanthenes with Azoles. And the article contained the following:

A new anode strategy for accessing xanthen-9-azoles via an electrochem. C(sp3)-H/N-H cross-coupling of xanthenes with azoles is described. This reaction proceeds efficiently with a broad scope of both xanthenes and N-H-free azoles under metal- and addnl. oxidant-free conditions and represents a new access to direct incorporation of important N-heterocycle units into the resulting xanthenes. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).HPLC of Formula: 5301-96-2

The Article related to xanthenazole preparation electrochem cross coupling xanthene azole, intermol anodic oxidative cross dehydrogenative coupling, Heterocyclic Compounds (More Than One Hetero Atom): General and other aspects.HPLC of Formula: 5301-96-2

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

On April 4, 2019, Ge, Jhih Kuei; Lee, Yi-Chia; Liu, Wen Dar; Kuo, Chi-Hsien published a patent.COA of Formula: C9H9N3 The title of the patent was Stripper solutions and methods of using stripper solutions. And the patent contained the following:

The invention relates to a stripper solution for removing a resist from a substrate, comprising one or more than one organic solvent, water, hydroxylamine or one or more than one derivative of hydroxylamine, one or more than one corrosion inhibitor, optional one or more than one surfactant, and one or more than one quaternary ammonium hydroxide, wherein the quaternary ammonium hydroxide has the formula: R2-N(R1)(R3)-R4, wherein R1, R2, R3, and R4 are alkyl groups, benzyl, aryl groups, or a combination thereof having collectively at least 5 carbons. The invention also relates to a method for removing a resist from a substrate, comprising; (a) providing a substrate having a resist thereon; (b) contacting the substrate with a stripper solution for a time sufficient to remove the resist; (c) removing the substrate from the stripping solution; and {d} rinsing the stripper solution from the substrate with a solvent. An electronic device prepared according to the inventive method is also claimed. The invention also claims a method for preparing a stripper solution, comprising: (a) providing a container; (b) providing components of the stripper solution composition; and (c) adding components of stripper solution to container to provide contents. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).COA of Formula: C9H9N3

The Article related to cleaning composition stripper photoresist removal electronic device fabrication, Surface Active Agents and Detergents: Cleaning Compositions and other aspects.COA of Formula: C9H9N3

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

On April 4, 2019, Ge, Jhih Kuei; Lee, Yi-Chia; Liu, Wen Dar; Kuo, Chi-Hsien published a patent.Related Products of 5301-96-2 The title of the patent was Stripper solutions and methods of using stripper solutions. And the patent contained the following:

The invention relates to a stripper solution for removing a resist from a substrate, comprising one or more than one organic solvent, water, hydroxylamine or one or more than one derivative of hydroxylamine, one or more than one corrosion inhibitor, optional one or more than one surfactant, and one or more than one quaternary ammonium hydroxide, wherein the quaternary ammonium hydroxide has the formula: R2-N(R1)(R3)-R4, wherein R1, R2, R3, and R4 are alkyl groups, benzyl, aryl groups, or a combination thereof having collectively at least 5 carbons. The invention also relates to a method for removing a resist from a substrate, comprising; (a) providing a substrate having a resist thereon; (b) contacting the substrate with a stripper solution for a time sufficient to remove the resist; (c) removing the substrate from the stripping solution; and {d} rinsing the stripper solution from the substrate with a solvent. An electronic device prepared according to the inventive method is also claimed. The invention also claims a method for preparing a stripper solution, comprising: (a) providing a container; (b) providing components of the stripper solution composition; and (c) adding components of stripper solution to container to provide contents. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Related Products of 5301-96-2

The Article related to cleaning composition stripper photoresist removal electronic device fabrication, Surface Active Agents and Detergents: Cleaning Compositions and other aspects.Related Products of 5301-96-2

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

Tome, A. C. published an article in 2004, the title of the article was Product class 13: 1,2,3-triazoles.Computed Properties of 5301-96-2 And the article contains the following content:

A review. Methods to prepare 1,2,3-triazoles are reviewed including cyclization, aromatization, ring transformation and substituent modification. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Computed Properties of 5301-96-2

The Article related to review triazole preparation cyclization aromatization ring transformation, Heterocyclic Compounds (More Than One Hetero Atom): Reviews and other aspects.Computed Properties of 5301-96-2

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

On December 31, 2018, Lee, Dong-Hwan; Hasanuzzaman, M.; Kwon, Daeho; Choi, Hye-Young; Kim, So Myoung; Kim, Dong Jin; Kang, Dong Ju; Hwang, Tae-Ho; Kim, Hyung-Hoi; Shin, Ho Jung; Shin, Jae-Gook; Oh, Sangtae; Lee, Seokjoon; Kim, So Won published an article.Recommanded Product: 5301-96-2 The title of the article was 10-Phenyltriazoyl Artemisinin is a Novel P-glycoprotein Inhibitor that Suppresses the Overexpression and Function of P-glycoprotein. And the article contained the following:

The effect of drugs on ATP-binding cassette transporters, especially permeability-glycoprotein (P-gp), is an important consideration during new anti-cancer drug development. In this context, the effects of a newly synthesized artemisinin derivative, 10-(4-phenyl-1H-1,2,3- triazol)-artemisinin (5a), were evaluated on P-gp expression and function. Reverse transcript polymerase chain reaction and immunoblotting techniques were used to determine the effect of 5a on P-gp expression in LS174T cells. In addition, the ability of 5a to work as either a substrate or an inhibitor of P-gp was investigated through different methods. The results revealed that 5a acts as a novel P-gp inhibitor that dually suppresses the overexpression and function of P-glycoprotein. Co-treatment of LS174T cell line, human colon adenocarcinoma cell line, with 5a and paclitaxel recovered the anticancer effect of paclitaxel by controlling the acquired drug resistance pathway. The overexpression of P-gp induced by rifampin and paclitaxel in a colorectal cell line was suppressed by 5a which could be a novel inhibitory substrate inhibiting the transport of paclitaxel by P-gp. The results revealed that 5a can be classified as a type B P-gp inhibitor (with both substrate and inhibitor activities) with an addnl. function of suppressing P-gp overexpression. The results might be clin. useful in the development of anticancer drugs against cancers with multidrug resistance. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Recommanded Product: 5301-96-2

The Article related to glycoprotein inhibitor anticancer agent colon adenocarcinoma, artemisinin, immunoblotting techniques, p-glycoprotein, paclitaxel, rifampin, triazolyl artemisinin., Pharmacology: Effects Of Antimicrobials and Parasiticides and other aspects.Recommanded Product: 5301-96-2

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

On February 20, 2011, Lee, Seokjoon published an article.Synthetic Route of 5301-96-2 The title of the article was Synthesis of 10β-substituted triazolyl artemisinins and their growth inhibitory activity against various cancer cells. And the article contained the following:

A library of 10-triazolylartemisinins was established comprising compounds that strongly inhibit the growth of cancer cell lines, such as DLD-1, U-87, Hela, SiHa, A172, and Bi1. These compounds were synthesized by an acid-catalyzed reaction of dihydroartemisinin (I) with various triazoles in CH2Cl2 at room temperature In particular, when 3 equivalent of triazole were reacted with I, 10β-(4-substituted triazolyl)artemisinins were obtained, which means that the type of product obtained differs according to the quantity of triazole reactant employed in the synthesis. From the viewpoint of antiproliferative activity against the various cancer cells, compounds, which have a (pentylphenyl)triazole moiety, exhibited potent activity. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Synthetic Route of 5301-96-2

The Article related to triazolylartemisinin preparation anticancer, artemisinin triazole preparation anticancer, Terpenes and Terpenoids: Sesquiterpenes (C15), Including Ionones and other aspects.Synthetic Route of 5301-96-2

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

On July 15, 2010, Oh, Sangtae; Shin, Woon-Seob; Ham, Jungyeob; Lee, Seokjoon published an article.HPLC of Formula: 5301-96-2 The title of the article was Acid-catalyzed synthesis of 10-substituted triazolyl artemisinins and their growth inhibitory activity against various cancer cells. And the article contained the following:

A diastereomeric and regioisomeric library of 10-triazolylartemisinins with potent growth-inhibitory activities against various cancer cell lines was established. These compounds were synthesized by the reaction with dihydroartemisinin and various triazoles in CH2Cl2 using BF3.OEt2 catalyst. Most of the compounds exhibited a strong potency in the submicromolar range, and, in particular, 3 compounds, having a (pentylphenyl)triazole moiety, proved to be promising candidates for preclin. trials. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).HPLC of Formula: 5301-96-2

The Article related to triazole artemisinin preparation anticancer, Terpenes and Terpenoids: Sesquiterpenes (C15), Including Ionones and other aspects.HPLC of Formula: 5301-96-2

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

On May 31, 1980, Boev, V. I.; Kushnir, V. N.; Shevchuk, M. I.; Dombrovskii, A. V. published an article.Recommanded Product: 5301-96-2 The title of the article was Synthesis and properties of 1,2,3-triazoles containing a ferrocenyl nucleus. And the article contained the following:

The title compounds I (R1 = H, Me, MeO, Cl, Br, NO2, R2 = H; R1 = H, R2 = Me; Fc = ferrocenyl) were prepared in 57-77% yields by cyclizing Ph3P:CR2COR1 with FcSO2N3. Treating I with EtOH gave 96-99% II. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Recommanded Product: 5301-96-2

The Article related to ferrocenyl triazole, triazole ferrocenylsulfonyl, Organometallic and Organometalloidal Compounds: Iron Compounds and other aspects.Recommanded Product: 5301-96-2

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