Category: 5301-96-2

On February 29, 2016, Wu, Luyong; Wang, Xianghui; Chen, Yuxue; Huang, Qinglan; Lin, Qiang; Wu, Mingshu published an article.Recommanded Product: 4-(p-Tolyl)-1H-1,2,3-triazole The title of the article was 4-Aryl-NH-1,2,3-Triazoles via Multicomponent Reaction of Aldehydes, Nitroalkanes, and Sodium Azide. And the article contained the following:

4-Aryl-NH-1,2,3-triazoles are valuable compounds in organic chem. and pharmaceutical chem. In this paper, we describe a novel multicomponent reaction of aldehydes, nitroalkanes, and sodium azide for the synthesis of 4-aryl-NH-1,2,3-triazoles. In this transformation, it was found that both the slow addition of nitroalkane and the presence of NaHSO3/Na2SO3 are advantageous to promote the reaction results. Addnl., a series of aldehydes and nitro compounds were investigated. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Recommanded Product: 4-(p-Tolyl)-1H-1,2,3-triazole

The Article related to aryl triazole multicomponent preparation aldehyde nitroalkane sodium azide, Heterocyclic Compounds (More Than One Hetero Atom): Other 5-Membered Rings, Two Or More Hetero Atoms and other aspects.Recommanded Product: 4-(p-Tolyl)-1H-1,2,3-triazole

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

Chavan, Omprakash S. published an article in 2022, the title of the article was Comparative study of various synthetic methods of 1,2,3-triazoles via click reaction: a mini review.Recommanded Product: 4-(p-Tolyl)-1H-1,2,3-triazole And the article contains the following content:

Different derivatives of azides were condensed with different derivatives of terminal alkynes via click condensation reaction to form resp. derivatives of 1,2,3-triazoles in various reaction conditions. Present paper deals with the comparative study of synthesis of derivatives of 1,2,3-triazoles with respect to yield, reaction time and reaction conditions. All products were characterized by spectral data and elemental anal. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Recommanded Product: 4-(p-Tolyl)-1H-1,2,3-triazole

The Article related to alkyne azide condensation reaction green chem, triazole preparation, Heterocyclic Compounds (More Than One Hetero Atom): Other 5-Membered Rings, Two Or More Hetero Atoms and other aspects.Recommanded Product: 4-(p-Tolyl)-1H-1,2,3-triazole

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

Zhu, Li-Li; Tian, Lifang; Cai, Bin; Liu, Guanglu; Zhang, Hui; Wang, Yahui published an article in 2020, the title of the article was Diamine-mediated N2-selective β-selenoalkylation of triazoles with alkenes.Name: 4-(p-Tolyl)-1H-1,2,3-triazole And the article contains the following content:

A N2-selective β-selenoalkylation of 1,2,3-triazoles with alkenes mediated by diamines has been developed. The reaction proceeds presumably via the interaction of diamines with both the triazole moiety and selenium/alkene complex to construct a U-shaped reaction intermediate. This activation mode will block the N1 position on triazoles and thus favor the N2-selective selenoamination. This stereospecific anti-addition method enables an efficient N2-selective β-selenoalkylation of 1,2,3-triazoles under mild and open-air conditions and might find applications in the synthesis of biol. active mols. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Name: 4-(p-Tolyl)-1H-1,2,3-triazole

The Article related to triazole derivative regioselective preparation, alkene triazole regioselective selenoalkylation diamine, Heterocyclic Compounds (More Than One Hetero Atom): Other 5-Membered Rings, Two Or More Hetero Atoms and other aspects.Name: 4-(p-Tolyl)-1H-1,2,3-triazole

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

On December 15, 2010, Jiang, Yubo; Kuang, Chunxiang; Yang, Qing published an article.Safety of 4-(p-Tolyl)-1H-1,2,3-triazole The title of the article was Copper(I) iodide-catalyzed synthesis of 4-aryl-1H-1,2,3-triazoles from anti-3-aryl-2,3-dibromopropanoic acids and sodium azide. And the article contained the following:

4-Aryl-1H-1,2,3-triazoles were synthesized from anti-3-aryl-2,3-dibromopropanoates and NaN3 by using inexpensive CuI as the catalyst in DMSO. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Safety of 4-(p-Tolyl)-1H-1,2,3-triazole

The Article related to bromopropanoate sodium azide cyclization cuprous iodide catalyst, triazole aryl preparation, Heterocyclic Compounds (More Than One Hetero Atom): Other 5-Membered Rings, Two Or More Hetero Atoms and other aspects.Safety of 4-(p-Tolyl)-1H-1,2,3-triazole

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

On September 13, 2004, Jin, Tienan; Kamijo, Shin; Yamamoto, Yoshinori published an article.Formula: C9H9N3 The title of the article was Copper-catalyzed synthesis of N-unsubstituted 1,2,3-triazoles from nonactivated terminal alkynes. And the article contained the following:

The [3 + 2]-cycloaddition of nonactivated terminal alkynes and trimethylsilyl azide proceeded smoothly in the presence of Cu1 catalyst to give N-unsubstituted triazoles, e.g., I, in good to high yields. The reaction most probably proceeded through the in situ formation of a copper acetylide species and hydrazoic acid, followed by a successive [3 + 2]-cycloaddition reaction. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Formula: C9H9N3

The Article related to alkyne silyl azide cycloaddition copper, triazole preparation, copper cycloaddition catalyst, Heterocyclic Compounds (More Than One Hetero Atom): Other 5-Membered Rings, Two Or More Hetero Atoms and other aspects.Formula: C9H9N3

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

On July 13, 2017, Hoffman, Thomas James; Stierli, Daniel; Jeanguenat, Andre; Beaudegnies, Renaud; Pouliot, Martin published a patent.Synthetic Route of 5301-96-2 The title of the patent was Preparation of microbicidal oxadiazole derivatives useful as pesticides and fungicides. And the patent contained the following:

The invention relates to preparation of oxadiazoles of formula I wherein all the variables areas defined in the disclosure, useful as pesticides, especially fungicides. The example compound II was prepared according the disclosed procedure and was tested for its antifungal activity against various microorganisms in agricultural plants (data shown). Compounds I can be used in agrochem. as pesticides and fungicides. 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 oxadiazole derivative preparation agricultural pesticide fungicide plant microbial infection, Heterocyclic Compounds (More Than One Hetero Atom): Other 5-Membered Rings, Two Or More Hetero Atoms and other aspects.Synthetic Route of 5301-96-2

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

Wang, Xiaokun; Kuang, Chunxiang; Yang, Qing published an article in 2012, the title of the article was Copper-catalyzed synthesis of 4-aryl-1H-1,2,3-triazoles from 1,1-dibromoalkenes and sodium azide.Application In Synthesis of 4-(p-Tolyl)-1H-1,2,3-triazole And the article contains the following content:

A methodol. for the Cu-catalyzed synthesis of 1H-1,2,3-triazoles from 1,1-dibromoalkenes and sodium azide is presented. Aryl dibromoolefins were efficiently converted into the corresponding 1,2,3-triazoles. A comprehensive number of functional groups were compatible with this reaction. 1,2,3-Triazoles were obtained in moderate to excellent yields. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Application In Synthesis of 4-(p-Tolyl)-1H-1,2,3-triazole

The Article related to aryltriazole preparation, aryldibromoalkene sodium azide dipolar cycloaddition copper catalyst, Heterocyclic Compounds (More Than One Hetero Atom): Other 5-Membered Rings, Two Or More Hetero Atoms and other aspects.Application In Synthesis of 4-(p-Tolyl)-1H-1,2,3-triazole

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

On August 6, 2021, Garg, Anirban; Hazarika, Roktopol; Dutta, Nilakshi; Dutta, Bidyutjyoti; Sarma, Diganta published an article.Name: 4-(p-Tolyl)-1H-1,2,3-triazole The title of the article was Bio-waste Derived Catalytic Approach Towards NH-1,2,3-Triazole Synthesis. And the article contained the following:

A bio-waste derived catalyst towards the synthesis of 4-aryl-NH-1,2,3-triazoles were reported. Whey was used as an efficient bio-waste derived catalyst for straight forward synthesis of NH-1,2,3-triazoles under very mild condition. The method was highly versatile, inexpensive, offered various NH-1,2,3-triazoles in good to excellent yields. The solvent-catalyst combination was effectively reused up to 4th consecutive cycles without significant loss in its catalytic efficiency. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Name: 4-(p-Tolyl)-1H-1,2,3-triazole

The Article related to azide aryl aldehyde biowaste whey catalyst heterocyclization green chem, aryl triazole preparation, Heterocyclic Compounds (More Than One Hetero Atom): Other 5-Membered Rings, Two Or More Hetero Atoms and other aspects.Name: 4-(p-Tolyl)-1H-1,2,3-triazole

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

Ramkumar, Rajagopal; Chandrasekaran, Srinivasan published an article in 2018, the title of the article was Efficient Catalyst-Free Trans Sulfonamidation/Sulfonamide Metathesis under Mild Conditions.Recommanded Product: 5301-96-2 And the article contains the following content:

An efficient, catalyst-free chemoselective protocol for the N-tosyl metathesis of 1,2,3-triazoles/N-tosyl heteroaromatic compounds with various amines at room temperature is reported. This effective procedure would be useful for the detosylation of 1,2,3-triazoles/ N-tosyl heteroaromatic compounds as well as N-tosylation of amines. 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 triazole tosyl heteroaromatic compound amine chemoselective sulfonamidation sulfonamide metathesis, Heterocyclic Compounds (More Than One Hetero Atom): Other 5-Membered Rings, Two Or More Hetero Atoms and other aspects.Recommanded Product: 5301-96-2

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

Tiwari, Vibha; Bingham, Jacob T.; Vyas, Shubham; Singh, Anand published an article in 2020, the title of the article was Intermolecular fluoroamination of allenes towards substituted vinyl fluorides.Product Details of 5301-96-2 And the article contains the following content:

A synthetic method towards fluorinated allylamines e.g., I, using allene precursors is reported. A variety of heterocyclic amines such as benzotriazole, 4-phenyl-1H-1,2,3-triazole, 5-phenyl-1H-1,2,3,4-tetrazole, etc. were employed as nucleophiles in a Selectfluor promoted intermol. fluoroamination reaction. This strategy provides a novel synthetic route to access vinyl fluorides with a vicinal amine moiety e.g., I. The experimental process involved the reaction of 4-(p-Tolyl)-1H-1,2,3-triazole(cas: 5301-96-2).Product Details of 5301-96-2

The Article related to allene selectfluor triazole regioselective fluoroamination, tetrazole allene selectfluor fluoroamination, Heterocyclic Compounds (More Than One Hetero Atom): Other 5-Membered Rings, Two Or More Hetero Atoms and other aspects.Product Details of 5301-96-2

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