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6-methyl-2-phenyl[1,2,4]triazolo[1,5-a]pyridine is a complex organic chemical compound with the molecular formula C13H10N4. It belongs to the class of triazolo[1,5-a]pyridine derivatives, which are heterocyclic compounds containing a triazole ring fused to a pyridine ring. The structure of 6-methyl-2-phenyl[1,2,4]triazolo[1,5-a]pyridine features a methyl group at the 6th position and a phenyl group at the 2nd position, which are both attached to the triazolopyridine core. 6-methyl-2-phenyl[1,2,4]triazolo[1,5-a]pyridine has potential applications in medicinal chemistry and material science, as it may exhibit unique biological activities or properties due to its specific molecular structure. However, further research and characterization are needed to fully understand its potential uses and properties.

4931-26-4

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4931-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4931-26-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,3 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4931-26:
(6*4)+(5*9)+(4*3)+(3*1)+(2*2)+(1*6)=94
94 % 10 = 4
So 4931-26-4 is a valid CAS Registry Number.

4931-26-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-2-phenyl-[1,2,4]triazolo[1,5-a]pyridine

1.2 Other means of identification

Product number -
Other names 6-Methyl-2-phenyl-s-triazolo<1,5-a>pyridin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4931-26-4 SDS

4931-26-4Downstream Products

4931-26-4Relevant academic research and scientific papers

Synthetic method 1, 2 and 4 - triazole compound

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Paragraph 0030-0033, (2021/12/07)

The invention discloses 1. 2,4 - Triazole compound synthesis method belongs to the technical field of synthesis of triazole compounds. After the reaction is finished, the reaction is carried out under the heating condition, and the target product 1, 2 and

A Convenient Synthesis of 1,5-Fused 1,2,4-Triazoles from N-Arylamidines via Chloramine-T Mediated Intramolecular Oxidative N-N Bond Formation

Bhatt, Ashish,Kant, Ravi,Sarma, Bhupendra K.,Singh, Rajesh K.

, p. 3883 - 3890 (2019/10/11)

A convenient synthesis of 1,5-fused 1,2,4-triazoles from readily available N-arylamidines is reported. The reaction is efficiently promoted by chloramine-T to afford the desired products mostly in high yields and in relatively short time, through direct m

Trichloroisocyanuric acid-mediated synthesis of 1,5-fused 1,2,4-triazoles from N-heteroaryl benzamidines via intramolecular oxidative N–N bond formation

Bhatt, Ashish,Singh, Rajesh K.,Sarma, Bhupendra K.,Kant, Ravi

supporting information, (2019/08/13)

A convenient synthesis of 1,5-fused 1,2,4-triazoles from readily available N-heteroaryl benzamidines is reported. The reaction is efficiently promoted by trichloroisocyanuric acid to afford the desired products, mostly in high yields and in relatively sho

Intramolecular electrochemical dehydrogenative N-N bond formation for the synthesis of 1,2,4-triazolo[1,5-a] pyridines

Li, Yong,Ye, Zenghui,Chen, Na,Chen, Zhenkun,Zhang, Fengzhi

supporting information, p. 4035 - 4039 (2019/08/07)

A metal- and oxidant-free intramolecular dehydrogenative N-N bond formation has been developed under mild and scalable electrolytic conditions. Various valuable 1,2,4-triazolo[1,5-a]pyridines were synthesized efficiently from the readily available N-(2-pyridyl)amidines. The reactions were conducted in a simple undivided cell under constant current conditions with nBu4NBr as both the redox mediator and the electrolyte. This protocol was applied to the efficient synthesis of key intermediates for anti-diabetic compounds.

I2/KI-Mediated Oxidative N-N Bond Formation for the Synthesis of 1,5-Fused 1,2,4-Triazoles from N -Aryl Amidines

Song, Lina,Tian, Xianhai,Lv, Zhigang,Li, Ertong,Wu, Jie,Liu, Yangxue,Yu, Wenquan,Chang, Junbiao

, p. 7219 - 7225 (2015/07/28)

An I2/KI-mediated oxidative N-N bond formation reaction is described. This new and environmentally benign approach allows for the convenient synthesis of a variety of 1,2,4-triazolo[1,5-a]pyridines and other 1,5-fused 1,2,4-triazoles from readi

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