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1-(N-(4-chlorophenyl)carbamoyl)benzotriazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39764-22-2

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39764-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39764-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,6 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39764-22:
(7*3)+(6*9)+(5*7)+(4*6)+(3*4)+(2*2)+(1*2)=152
152 % 10 = 2
So 39764-22-2 is a valid CAS Registry Number.

39764-22-2Relevant academic research and scientific papers

Novel urea and bis-urea primaquine derivatives with hydroxyphenyl or halogenphenyl substituents: Synthesis and biological evaluation

Perkovi?,Antunovi?,Marijanovi?,Pavi?,Ester,Kralj,Vlaini?,Kosalec,Schols,Hadjipavlou-Litina,Pontiki,Zorc

, p. 622 - 636 (2016/09/14)

A series of novel compounds 3a-j and 6a-j with primaquine and hydroxyl or halogen substituted benzene moieties bridged by urea or bis-urea functionalities were designed, synthesized and evaluated for biological activity. The title compounds were prepared

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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