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N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86298-24-0

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86298-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86298-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,9 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86298-24:
(7*8)+(6*6)+(5*2)+(4*9)+(3*8)+(2*2)+(1*4)=170
170 % 10 = 0
So 86298-24-0 is a valid CAS Registry Number.

86298-24-0Relevant academic research and scientific papers

Simple, novel synthesis for 1-carbamoyl-lH-benzotriazole and some of its analogs

Perry, Christopher John,Holding, Keith,Tyrrell, Elizabeth

, p. 3354 - 3365 (2008)

1-Carbamoyl-1H-benzotriazole (benzotriazole-1-carboxamide, 2a), an effective carbamoyl chloride substitute, and a range of its analogs can be synthesized in good yields in two very simple steps from 1,2-diaminobenzene. The facile preparation of the interm

P(III)-Assisted Electrochemical Access to Ureas via in situ Generation of Isocyanates from Hydroxamic Acids

Meng, Haiwen,Sun, Kunhui,Xu, Zhimin,Tian, Lifang,Wang, Yahui

, p. 1768 - 1772 (2021/03/26)

An external oxidant-free protocol for the generation of isocyanates from hydroxamic acids assisted by trivalent phosphine under mild electrochemical conditions was reported. The process started with the anodic oxidation of hydroxamic acids, followed by reacting with phosphine to form corresponding alkoxyphosphoniums and subsequent rearrangement with the release of tri-substituted phosphine oxide as the driving force to give isocyanates, which were trapped by N-based nucleophiles to produce various ureas. This method provides a broadly applicable procedure to access isocyanate intermediates under mild electrochemical conditions.

One-pot preparation of carbamoyl benzotriazoles and their applications in the preparation of ureas, hydrazinecarboxamides and carbamic esters

Mao, Hui,Liu, Huili,Tu, Yawei,Zhong, Zhiyun,Lv, Xin,Wang, Xiaoxia

, p. 13 - 22 (2016/02/18)

Carbamoyl benzotriazoles were conveniently synthesized in one-pot from carboxylic acids, diphenyl phosphorazidate (DPPA) and 1H-benzotriazole (BtH). The reactivity and applications of carbamoyl benzotriazoles were also explored. Carbamoyl benzotriazoles react smoothly with amino acids, hydrazines and alcohols, thus providing facile access to the corresponding ureas, hydrazinecarboxamides and carbamic esters, respectively, in good to excellent yields.

PHARMACEUTICAL COMPOUNDS

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Page/Page column 184, (2012/03/27)

The invention relates to compounds and compositions for inhibiting the enzyme fatty acid amide hydrolase (FAAH), the use of the compounds in therapy and, in particular, for treating or preventing conditions whose development or symptoms are linked to subs

Trapping! of isocyanates with benzotriazole in situ - Preparation of carbamoyl benzotriazoles as an isocyanate alternative via curtius rearrangement

Zhong, Zhiyun,Wang, Xiaoxia,Kong, Lichun,Zhu, Xiangming

experimental part, p. 2461 - 2464 (2010/01/07)

N-Aryl and N-alkenyl carbamoyl benzotriazoles were prepared in good to excellent yields from acyl azides and benzotriazole via Curtius rearrangement, while N-alkylcarbamoyl benzotriazoles were formed from N-alkanoyl benzotriazoles and sodium azide in one

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