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N-[(1H-pyrazol-3-ylamino)carbonothioyl]benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34683-41-5

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34683-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34683-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,8 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34683-41:
(7*3)+(6*4)+(5*6)+(4*8)+(3*3)+(2*4)+(1*1)=125
125 % 10 = 5
So 34683-41-5 is a valid CAS Registry Number.

34683-41-5Downstream Products

34683-41-5Relevant academic research and scientific papers

Synthesis of Purine Analogues: Photocatalyst-Free Visible-Light-Enhanced Annulation Approach to Pyrazolo[1,5- A[[1,3,5]triazine-2,4-diamines

Guo, Wei,Xie, Zhen,Cai, Liuhuan,Liu, Gongping,Deng, Ling,Mei, Weijie,Zou, Xiaoying,Zhong, Yumei,Zhuo, Xiaoya,Zheng, Lvyin,Fan, Xiaolin

supporting information, p. 8365 - 8380 (2021/06/28)

A new photocatalyst-free visible-light-enhanced strategy for the synthesis of pyrazolo[1,5-a][1,3,5]triazine-2,4-diamines via the formation of electron donor-acceptor (EDA) complexes is reported. The in situ generated pyrazolthiourea intermediates from 1H-pyrazol-3-amines and isothiocyanates undergo formal [4 + 2] annulation with 1,1,3,3-tetramethylguanidines (TMG) to deliver the corresponding products involved in three C-N bond formations in a one-pot protocol. The formation of EDA complex from pyrazolthiourea and TMG is confirmed by UV-vis spectroscopy and 1H NMR experiments. Moreover, this mild reaction proceeds in the absence of any external transition metals, oxidants, bases, and ligands. This efficient methodology for the synthesis of purine analogues pyrazolo[1,5-a][1,3,5]triazine-2,4-diamines provides potential synthetic applications in the field of drug research and development.

THIAZOLE DERIVATIVES AND USE THEREOF

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Page/Page column 52-53, (2010/11/25)

The present invention is related to thiazole derivatives of Formula (I) in particular for the treatment and/or prophylaxis of autoimmune disorders and/or inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, bacterial or viral infections, kidney diseases, platelet aggregation, cancer, transplantation, graft rejection or lung injuries.

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